JP5849317B2 - Variety identification marker of vegetative propagation crop - Google Patents

Description

  The present invention relates to a DNA marker for distinguishing konjac main cultivars from other varieties / lines in konjac ginger and primary processed products, and a method for narrowing down konjac main cultivars candidates using the markers as targets.

Konjac is grown and cultivated mainly by vegetative breeding, and if you purchase a small quantity of excellent varieties first, you can produce high-quality konjac by self-propagation.
So far, varieties of konjac have been identified through appearance observations such as the leaf petals of the ground part, the color and shape of the leaflets, the shape of the corms and pupae. However, since these characteristics change according to the growth environment, they are only accurate to the extent that a variety is estimated from a plurality of characteristics, and cannot be used as a marker for reliably identifying the variety. In addition, the harvested corms are primarily processed into coarse powder and fine powder, but there was no means for identifying the variety in these processed products. For this reason, it was not possible to prevent or regulate the varieties of high quality varieties overseas, which could have a serious impact on the domestic konjac industry.

  Regarding the application of molecular biological techniques in recent years, Gunma Agricultural Technology Center conducted research on varietal identification technology of konjac using RFLP method and RAPD method from 1993 to 2013. However, it was extremely difficult to detect a stable DNA polymorphism, and no practical variety identification marker was obtained. For this reason, it has been extremely difficult to identify the four main varieties of Konjac “Akagi Odama”, “Harunakuro”, “Myogi Yutaka”, and “Miyama Sari”.

"Development of konjac varieties identification marker" Tomoaki Noguchi, Ayako Hosoe, Tomoko Takamiya, Hiroaki Iizuka, Yasufumi Murakami, Shuji Yamashita, Hisato Okuizumi DNA polymorphism vol.15 p.154-158, 2007 `` Development of konjac varieties distinguishing codominant marker using RLGS method '' Tomoaki Noguchi, Akiko Hosogaki, Tomoko Takamiya, Hiroaki Iizuka, Shuji Yamashita, Yasufumi Murakami, Hisato Okuizumi DNA polymorphism vol.16 p.65-71, 2008

  The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a DNA marker specific to varieties of konjac using a molecular biological technique. The present invention also provides a method for narrowing down konjac cultivar candidates using the marker as a target, reagents and kits for use in the method, oligonucleotides usable in the method, a set of oligonucleotides usable in the method, and the like. This is the issue.

  The present inventors have intensively studied to solve the above problems. The inventors of the present invention used the restriction enzyme landmark genome scanning method (RLGS method; Patent No. 1) for the four main cultivars of konjac (Akagi Odama, Harukuroro, Myougi Yutaka, Miyama Sari), and one other line (a Chinese species). In this way, we succeeded in detecting a total of 38 specific DNA fragments between cultivars and strains. The present inventors have analyzed a specific DNA fragment between varieties and strains, and found that by using the genotype contained in the DNA fragment as an index, candidate konjac cultivar candidates can be narrowed down. It was.

Specifically, the present inventors specifically amplify a DNA fragment showing a polymorphism between cultivars / lines from the nucleotide sequence information contained in the DNA fragments specific between varieties / lines obtained by the RLGS method. Three possible pairs of primers (SEQ ID NOs: 1-6) were synthesized. PCR using the primer pairs designed using the konjac main cultivars “Akagi Odama”, “Harunuro”, “Myogi Yutaka”, “Miyama Sari” and one other strain (Chinese species) genomic DNA as a template. Went.
As a result of separating the obtained amplification products by electrophoresis, PCR fragments capable of identifying konjac cultivar candidates were detected, and it was found that konjac cultivar candidates could be determined using the PCR fragment length as an index. did.

Furthermore, the present inventors have succeeded in developing a CAPS marker for identifying four main cultivars. The present inventors designed a primer pair consisting of the nucleotide sequences set forth in SEQ ID NOs: 7 and 8, and performed PCR. Furthermore, the amplification product obtained by PCR was digested with the restriction enzyme HhaI.
As a result of separation of the obtained degradation products by electrophoresis, a DNA fragment capable of identifying a candidate for the konjac variety was detected, and it was found that the candidate for the konjac variety could be determined using the DNA fragment as an index. .

The present invention is based on such findings, and more specifically, relates to the inventions described in [1] to [17] below.
[1] A method for narrowing down candidate konjac varieties including the step of comparing the genotype described in (a) below and the genotype described in (b) below, wherein the genes compared in the above step A method of narrowing down the varieties of the control konjac as candidates for the varieties of the tested konjac when the types match;
(A) a genotype in the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari, wherein the genotype is specific to the control konjac, and (b) Genotype of the same DNA region as in (a) in the genomic DNA of konjac
[2] The method according to [1], wherein the genotype in the genomic DNA of the control konjac is a genotype of at least one DNA region selected from the group consisting of (1) to (3) below;
(1) a DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 1 and a base sequence complementary to the base sequence described in SEQ ID NO: 2;
(2) a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 4; and (3) SEQ ID NO: 5 A DNA sequence sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 6 and a base sequence complementary to the base sequence described in SEQ ID NO: 6,
[3] The method according to [2], wherein the genotype in the genomic DNA of the control konjac is the genotype of the DNA region described in (1) and (2) below;
(1) a base sequence complementary to the base sequence described in SEQ ID NO: 1, and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 2; and (2) SEQ ID NO: 3 A DNA sequence sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 4 and a base sequence complementary to the base sequence described in SEQ ID NO: 4,
[4] The method according to [2], wherein the genotype in the genomic DNA of the control konjac is the genotype of the DNA region described in (1) and (2) below;
(1) a base sequence complementary to the base sequence described in SEQ ID NO: 1, and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 2; and (2) SEQ ID NO: 5 A DNA sequence sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 6 and a base sequence complementary to the base sequence described in SEQ ID NO: 6,
[5] The method according to [2], wherein the genotype in the genomic DNA of the control konjac is the genotype of the DNA region described in (1) and (2) below;
(1) a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 4; and (2) SEQ ID NO: 5 A DNA sequence sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 6 and a base sequence complementary to the base sequence described in SEQ ID NO: 6,
[6] A method for narrowing down candidate konjac varieties comprising a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Miyama Sari, Kaki Odama or Miya Mama Sari is narrowed down as a candidate for the konjac varieties to be tested,
A method in which when the genotype described in (b) coincides with that of Harukuroro or Miyu Yutaka, the target of the tested konjac variety is narrowed down.
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 1 in the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence described in No. 2: a genotype specific to the control konjac, and (b) (a) in the genomic DNA of the test konjac Genotype of the same DNA region,
[7] A method for narrowing down candidates for the varieties of test konjac including the step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Ogaki Odama or Myougi Yutaka, Akao Odama or Myougi Yutaka is narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Harunakuro or Miyamakari, the candidate konjac variety is narrowed down to Harunakuro or Miyamakari;
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 3 in the genomic DNA of any konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 4, wherein the genotype is specific to the control konjac, and (b) in the genomic DNA of the test konjac (a ) Genotype of the same DNA region,
[8] A method for narrowing down candidate konjac varieties comprising a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Harukuroro, Akao Odama or Harukuro is narrowed down as a candidate for the varieties of konjac.
When the genotype described in (b) matches that of Miyuki Yutaka, Miyu Yutaka was narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Miyama Sari, Miyama Sari is narrowed down as a candidate for the varieties of test konjac;
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 5 in the genomic DNA of any konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 6, wherein the genotype is specific to the control konjac, and (b) in the genomic DNA of the test konjac (a ) Genotype of the same DNA region,
[9] A method for narrowing down candidate konjac varieties including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Miyama Sari, Kaki Odama or Miya Mama Sari is narrowed down as a candidate for the konjac varieties to be tested,
A method in which when the genotype described in (b) coincides with that of Harukuroro or Miyu Yutaka, the target of the tested konjac variety is narrowed down.
(A) a genotype specific to the control konjac in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and (ii) Genotype identified through the steps described in), and (b) genotype in the genomic DNA of the test konjac, (a) the genotype of the same DNA region as the control konjac,
(I) obtaining a DNA fragment comprising a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 8; And (ii) decomposing the DNA fragment obtained in step (i) with the restriction enzyme HhaI,
[10] A kit for narrowing down konjac variety candidates for use in the method according to any one of [1] to [9],
[11] SEQ ID NO: 1 an oligonucleotide comprising the nucleotide sequence of any one of 8
[12] At least one set selected from the group consisting of (A) to (D) below;
(A) an oligonucleotide comprising the base sequence described in SEQ ID NO: 1, and a set of oligonucleotides comprising the base sequence described in SEQ ID NO: 2,
(B) an oligonucleotide comprising the base sequence set forth in SEQ ID NO: 3 and a set of oligonucleotides comprising the base sequence set forth in SEQ ID NO: 4.
(C) comprising an oligonucleotide comprising the base sequence set forth in SEQ ID NO: 5 and a set of oligonucleotides comprising the base sequence set forth in SEQ ID NO: 6; and (D) comprising the base sequence set forth in SEQ ID NO: 7. A set of oligonucleotides and oligonucleotides comprising the base sequence set forth in SEQ ID NO: 8;
[13] A kit for narrowing down candidates for konjac varieties containing the oligonucleotide according to [11] or the set according to [12],
[14] The kit according to [13], further containing a restriction enzyme HhaI,
[15] Of the konjac varieties, selected from the group consisting of (i) to (iv) below, using as a template a konjac genomic DNA selected from the group consisting of Akagi Odama, Harunuroro, Myougi Yutaka, and Miyamasari DNA fragments amplified by PCR using at least one set as a primer set;
(I) an oligonucleotide comprising the nucleotide sequence set forth in SEQ ID NO: 1 and a set of oligonucleotides comprising the nucleotide sequence set forth in SEQ ID NO: 2.
(Ii) a set of oligonucleotides containing the base sequence set forth in SEQ ID NO: 3 and an oligonucleotide containing the base sequence set forth in SEQ ID NO: 4;
(Iii) an oligonucleotide containing the base sequence set forth in SEQ ID NO: 5 and a set of oligonucleotides containing the base sequence set forth in SEQ ID NO: 6; and (iv) a base sequence set forth in SEQ ID NO: 7 A set of oligonucleotides and oligonucleotides comprising the base sequence set forth in SEQ ID NO: 8;
[16] DNA fragment obtained by the steps described in (a) and (b) below;
(A) an oligonucleotide containing the nucleotide sequence of SEQ ID NO: 7 using as a template a konjac genomic DNA selected from the group consisting of konjac varieties Akagi Odama, Harunuro, Miyugi Yutaka, and Miyama Sari; And a step of amplifying a DNA fragment by PCR using a set of oligonucleotides containing the nucleotide sequence set forth in SEQ ID NO: 8 as a primer set, and (b) the DNA fragment obtained in step (a) is digested with restriction enzyme HhaI. Disassembling process,
[17] DNA comprising all or part of the base sequence described in any of SEQ ID NOs: 10-12, 14, 18-21 or a base sequence complementary to the base sequence.

According to the present invention, it has become possible to narrow down konjac cultivar candidates using molecular biological techniques. Conventionally, the varieties of konjac have been identified by appearance observation. However, since the appearance of konjac changes depending on the growth environment, there is a problem that the accuracy of variety identification is low. In addition, when konjac was processed, there was no means for identifying the variety.
In the present invention, varieties of konjac are identified using a DNA fragment specific to the variety as an index. Therefore, it is possible to determine varieties of konjac with high accuracy compared to identification using an appearance that is easily affected by the growth environment as an index. In addition, it is possible to predict the varieties of konjac even in the state of processed products that have been difficult to identify.

It is the figure and photograph which show the identification result (electrophoresis result) of a konjac variety using the variety identification primer kon601. It is a photograph which shows the identification result (electrophoresis result) of a konjac variety using the variety identification primer kon603. It is a photograph which shows the identification result (electrophoresis result) of a konjac variety using the variety identification primer kon272. It is a figure and a photograph which show the identification result (electrophoresis result) of a konjac variety using the kind identification primer kon601 CAPS.

  The present inventors analyzed specific DNA fragments between cultivars and strains obtained by the restriction enzyme landmark genome scanning method (RLGS method). As a result, the genotype contained in the DNA fragment was used as an index. They found that they could narrow down the varieties of konjacs to be tested. The present invention provides the following inventions based on such findings.

A method for narrowing down candidates for varieties of test konjac including the step of comparing the genotype described in (a) below and the genotype described in (b) below, wherein the genotypes compared in the step match When the control konjac varieties are narrowed down as candidates for the konjac varieties to be tested;
(A) a genotype in the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari, wherein the genotype is specific to the control konjac, and (b) Genotype of the same DNA region as in (a) in the genomic DNA of konjac.

Examples of “genotype in genomic DNA of control konjac” include “genotype of at least one DNA region selected from the group consisting of the following (1) to (3) in genomic DNA of control konjac”.
(1) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 1 and a base sequence complementary to the base sequence described in SEQ ID NO: 2.
(2) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a base sequence complementary to the base sequence described in SEQ ID NO: 4.
(3) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 5 and a base sequence complementary to the base sequence described in SEQ ID NO: 6.

In this method, when the genotype matches, the varieties of the control konjac are narrowed down as candidates for the varieties of the konjac to be tested.
If the genotype does not match, the control konjac variety is excluded from the candidate konjac varieties.

  In the present invention, the “genotype” means the kind (pattern) of allele. Therefore, the “genotype” of the present invention can also be expressed as an “allyl pattern”. The “allyl” of the present invention can also be expressed as “allele”, “allele”, or “polymorphism”.

  In the present invention, “genotype of at least one DNA region” includes a combination of genotypes of one DNA region and genotypes of a plurality of (for example, two or more) DNA regions. .

The “genotype specific to control konjac” in the present invention can also be expressed as “genotype specific to varieties of control konjac”.
The “DNA region genotype” can also be expressed as “a genotype present in the DNA region” or “a genotype present in a site on DNA”.
“DNA” can also be expressed as “double-stranded DNA”.

The control konjac in the present invention is a genotype of at least one DNA region selected from the group consisting of (1) to (3) above in the genomic DNA of the konjac, and a genotype specific to the konjac is detected. It is konjac. Examples of the control konjac include, but are not limited to, at least one konjac selected from the group consisting of 1 to 4 below. The following 1 to 4 konjacs and related konjacs and remote konjacs are also included in the control konjac of the present invention.
1. Akagi Odama (Agriculture and Forestry Certification Number: Konjac Agriculture and Forestry No. 1, Training Organization: Gunma Agricultural Technology Center)
2. Harunuroro (Agricultural and Forestry Certification Number: Konjac Agriculture and Forestry No. 2, Training Organization: Gunma Agricultural Technology Center)
3.Yuyo Yutaka (registration number: No. 9035, breeder right: Gunma Prefecture)
4. Miyama Sari (registration number: 13194, breeder right holder: Gunma Prefecture)
These control konjacs can be obtained from, for example, Gunma Agricultural Technology Center. It can also be obtained from a konjac farm.

  The “agricultural and forestry certification numbers” and “nurturing organizations” mean the agricultural and forestry certification numbers and the training organizations in the Japanese agricultural and forestry certification system (conventional naming registration system). In addition, “registration number” and “cultivator right holder” mean a registration number and a grower right holder in the Japanese variety registration system.

  In the present invention, the test konjac can be exemplified by plants having the characteristics of konjac, plants that have the potential of konjac, plant species that are genetically related to konjac, and processed products using these plants as raw materials. It is not limited to these. Examples of the processed product include, but are not limited to, raw potato slices, coarse powder, and fine powder.

  In addition, konjac has the characteristics of seed propagation by seeds and vegetative propagation by suckling and mucago. The stem is a corpus that is a vegetative body with enlarged stems, and the ground part has small leaves and petioles with one leaf changed. Although the plant comprised from can be illustrated, it is not limited to these.

  In addition, the “variety” in the present invention can also be expressed as “variety or breeding line” when the variety is registered. “Cultivar” in “Cultivar or breeding line” means a registered variety in the breed registration system, and “Growth line” in “Cultivar or breeding line” means an unregistered variety in the breed registration system (for example, before being established as a breed) Examples include those in the breeding stage and widely distributed systems).

In the present invention, “narrowing breed candidates” means “selecting breed candidates”, “identifying breed candidates”, “discriminating breed candidates”, “identifying breed candidates”, “breeds” Can be expressed as “determining a candidate for a product” or “determining a candidate for a variety”.
In the present invention, “narrow down product candidates” is expressed as “identify product types”, “identify product types”, “identify product types”, “identify product types”, or “determine product types”. You can also
In addition, “the genotype of the same DNA region as (a)” is expressed as “the genotype of a DNA region containing a genotype specific to the control konjac” and “the genotype identified through the same process as (a)”. You can also More specifically, for example,
(1) Genotype in a DNA region sandwiched by a base sequence complementary to the base sequence described in SEQ ID NO: 1 and a base sequence complementary to the base sequence described in SEQ ID NO: 2 (2) SEQ ID NO: The nucleotide sequence complementary to the nucleotide sequence described in 3, and the genotype in the DNA region sandwiched by the nucleotide sequence complementary to the nucleotide sequence described in SEQ ID NO: 4 (3) The nucleotide sequence described in SEQ ID NO: 5 And a genotype in a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 6 and the like.

  The present invention can be expressed in another form as follows. In addition, the inventions exemplified in the present specification as specific embodiments of the present invention and the inventions arbitrarily combining these inventions can also be expressed in the following forms.

The genotype described in (a) and the genotype described in (b) below match the genotype described in (a), including the step of comparing the genotype described in (a) below and the genotype described in (b) below. How to determine whether or not;
(A) At least one DNA region selected from the group consisting of (1) to (3) above in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari A genotype specific to the control konjac, and (b) a genotype of the same DNA region as (a) in the genomic DNA of the test konjac.
If it is determined that the genotypes match, the varieties of the control konjac are narrowed down as candidates for the varieties of the test konjac.

  The present invention can be expressed in another form as follows. In addition, the inventions exemplified in the present specification as specific embodiments of the present invention and the inventions arbitrarily combining these inventions can also be expressed in the following forms.

A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
A method in which the varieties of the control konjac are selected as candidates for the varieties of the tested konjac when the genotypes compared in the step match;
(A) consisting of Akagi Odama, Harunaroro, Myougi Yutaka, and Miyama Sari, which are the amplification targets of PCR using at least one set selected from the group consisting of (A) to (C) below as a primer set A genotype in the genomic DNA of a control konjac selected from the group, the genotype specific to the control konjac,
(B) the genotype of the same DNA region as (a) in the genomic DNA of the test konjac,
(A) an oligonucleotide comprising the base sequence described in SEQ ID NO: 1, and a set of oligonucleotides comprising the base sequence described in SEQ ID NO: 2,
(B) an oligonucleotide comprising the base sequence set forth in SEQ ID NO: 3 and a set of oligonucleotides comprising the base sequence set forth in SEQ ID NO: 4; and (C) a base sequence set forth in SEQ ID NO: 5 A set of oligonucleotides and oligonucleotides comprising the base sequence set forth in SEQ ID NO: 6.

  In the present invention, the word “consisting of” can be used instead of the word “including”.

  The present invention can be expressed in another form as follows. In addition, the inventions exemplified in the present specification as specific embodiments of the present invention and the inventions arbitrarily combining these inventions can also be expressed in the following forms.

A method for narrowing down the candidates for the varieties of test konjac including the step of comparing the types of PCR products described in (a) below and the types of PCR products described in (b) below. When the PCR product types match, the control konjac variety is selected as the candidate konjac variety to be tested;
(A) At least 1 selected from the group consisting of (A) to (C) above, using as a template the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari The kind of PCR product amplified by PCR using one set as a primer set, the kind of PCR product specific to the control konjac, and (b) the genomic DNA of the test konjac as a template, the same as (a) Types of PCR products amplified by PCR using the set as a primer set.

  In the present invention, “type of PCR product” means a PCR product pattern classified by the presence or absence of the PCR product or molecular size, and “type of PCR product” can be expressed as “PCR pattern”. “Type of PCR product (PCR pattern)” corresponds to “genotype (allele pattern)”.

  The present invention can be expressed in another form as follows. In addition, the inventions exemplified in the present specification as specific embodiments of the present invention and the inventions arbitrarily combining these inventions can also be expressed in the following forms.

A method of narrowing down the candidates for the varieties of the test konjac including the PCR product described in (a) below and the step of determining the identity of the PCR product described in (b) below. A method of narrowing down the varieties of the control konjac as candidates for the varieties of the tested konjac when they are identical;
(A) At least 1 selected from the group consisting of (A) to (C) above, using as a template the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari PCR product amplified by PCR using one set as a primer set, which is a PCR product specific to the control konjac and (b) genomic DNA of the test konjac as a template, and the same set as (a) is the primer set PCR product amplified by PCR.

In addition, the present invention is a method for narrowing down candidates for the varieties of the test konjac including the step of comparing the genotype described in (a) below and the genotype described in (b) below. Provided is a method for narrowing down the varieties of control konjac as candidates for the varieties of konjac to be tested when the genotypes matched.
(A) a genotype specific to the control konjac in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and (ii) Genotype identified through the steps described in), and (b) genotype in the genomic DNA of the test konjac, (a) the genotype of the same DNA region as the control konjac,
(I) obtaining a DNA fragment comprising a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 8; And (ii) a step of degrading the DNA fragment obtained in step (a) with the restriction enzyme HhaI.

  In the above invention, the definitions of “genotype”, “control konjac”, “test konjac”, “variety”, and “narrow down varieties of candidates” are as described above.

  In the above invention, “the genotype of the same DNA region as the control konjac of (a)” can also be expressed as “the genotype identified through the same steps as the control konjac of (a)”.

Moreover, the said invention can be expressed in another form as follows.
The genotype described in (a) and the genotype described in (b) below match the genotype described in (a), including the step of comparing the genotype described in (a) below and the genotype described in (b) below. How to determine whether or not;
(A) a genotype specific to the control konjac in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and (ii) Genotype identified through the steps described in), and (b) genotype in the genomic DNA of the test konjac, (a) the genotype of the same DNA region as the control konjac,
(I) obtaining a DNA fragment comprising a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 8; And (ii) a step of degrading the DNA fragment obtained in step (a) with the restriction enzyme HhaI.
If it is determined that the genotypes match, the varieties of the control konjac are narrowed down as candidates for the varieties of the test konjac.
If it is determined that the genotypes do not match, the varieties of the control konjac are excluded from the candidate varieties of the test konjac.

Moreover, the said invention can be expressed in another form as follows.
A method for narrowing down candidates for varieties of test konjac including the step of comparing the genotype described in (a) below and the genotype described in (b) below, wherein the genotypes compared in the step match A method of narrowing down the varieties of the control konjac as candidates for the varieties of konjac to be tested;
(A) a genotype specific to the control konjac in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and (ii) Genotype identified through the steps described in), and (b) genotype in the genomic DNA of the test konjac, (a) the genotype of the same DNA region as the control konjac,
(I) amplifying the genomic DNA of the control konjac using as a primer an oligonucleotide comprising the nucleotide sequence set forth in SEQ ID NO: 7 and an oligonucleotide comprising the nucleotide sequence set forth in SEQ ID NO: 8; ii) Decomposing the DNA fragment amplified in step (a) with the restriction enzyme HhaI.
In the present invention, the word “consisting of” can be used instead of the word “including”.

Moreover, the said invention can be expressed in another form as follows.
The method for narrowing down candidates for the varieties of konjac to be tested, including the step of comparing the types of restriction enzyme-treated products described in (a) below and the types of restriction enzyme-treated products described in (b) below, A method of narrowing down the varieties of the control konjac as candidates of the varieties of the tested konjac when the types of the restriction enzyme-treated products compared in the process match;
(A) a kind of restriction enzyme-treated product specific to the control konjac in the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and ( The type of restriction enzyme treatment product identified through the process described in ii), and (b) the type of restriction enzyme treatment product in the test konjac, identified through the same process as the control konjac in (a) Types of restriction enzyme treatment products,
(I) by PCR using the genomic DNA of control konjac as a template, and using as a primer set an oligonucleotide comprising the base sequence set forth in SEQ ID NO: 7 and an oligonucleotide set comprising the base sequence set forth in SEQ ID NO: 8 A step of amplifying the genomic DNA of the control konjac, and (ii) a step of degrading the DNA fragment amplified in step (a) with the restriction enzyme HhaI.

  In the above invention, "type of restriction enzyme treatment product" means a pattern of restriction enzyme HhaI treatment products classified according to molecular size, and "type of restriction enzyme treatment product" is "pattern of restriction enzyme treatment product". It can be expressed as “Type of restriction enzyme treatment product (restriction enzyme treatment product pattern)” corresponds to “genotype (allele pattern)”.

Moreover, the said invention can be expressed in another form as follows.
A method for narrowing down candidates for the varieties of konjac to be tested, including the step of determining the identity of the restriction enzyme-treated product described in (a) below and the restriction enzyme-treated product described in (b) below. A method of narrowing down the varieties of the control konjac as candidates for the varieties of the tested konjac when the restriction enzyme-treated products are the same in FIG.
(A) a kind of restriction enzyme-treated product specific to the control konjac in the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and ( ii) the type of restriction enzyme-treated product identified through the steps described in (ii), and (b) the type of restriction enzyme-treated product in the genomic DNA of the test konjac, through the same steps as the control konjac in (a) The type of restriction enzyme product identified,
(I) by PCR using the genomic DNA of control konjac as a template, and using as a primer set an oligonucleotide comprising the base sequence set forth in SEQ ID NO: 7 and an oligonucleotide set comprising the base sequence set forth in SEQ ID NO: 8 A step of amplifying the genomic DNA of the control konjac, and (ii) a step of degrading the DNA fragment amplified in step (a) with the restriction enzyme HhaI.

The present invention can be expressed in another form as follows.
A method for narrowing down candidates for a test konjac variety including the steps described in (a) to (c) below, when the restriction enzyme-treated products are the same, How to narrow down konjac varieties;
(A) The base sequence set forth in SEQ ID NO: 7 using as a template the genomic DNA of any control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari Amplifying genomic DNA of the control konjac and the test konjac by PCR using the oligonucleotide set comprising the oligonucleotide set comprising the nucleotide sequence set forth in SEQ ID NO: 8 as a primer set,
(B) a step of degrading the DNA fragment amplified in step (a) with restriction enzyme HhaI, and (c) a step of determining the identity of the restriction enzyme treatment product obtained in step (b).

Although the method of this invention is illustrated below, it is not limited to this.
In the present invention, first, at least one selected from the group consisting of (1) to (3) in the genomic DNA for each konjac selected from Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari Detect genotypes present in the DNA region. Next, a specific or specific konjac among varieties and strains of konjac (hereinafter referred to as genotype X), and a DNA region indicating the genotype X (hereinafter referred to as DNA region Y) Identified). The specific or one variety of konjac is used as a control konjac. Next, in the genomic DNA of the test konjac, the genotype (hereinafter referred to as genotype Z) of the same DNA region as the DNA region Y is identified. Next, genotype X and genotype Z are compared. When the compared genotypes match, the varieties of control konjac are narrowed down as candidates for the varieties of test konjac.

  Specifically, first, a primer for amplifying any DNA region selected from the group consisting of (1) to (3) by PCR is designed. When designing a primer, it is preferable that the length of the primer is about 20 bp and the Tm value is about 55 to 60 ° C. However, the present invention is not limited to this. Primers can be designed by Primer 3 (Rozen and Skaletsky, 2000, In: Krawets and Misener (eds.) Bioinfomatics Methods and Protocols: Methods in Molecular Biology, Totowa, NJ, USA: Humana Press, 365-386). PCR amplification using any set selected from the group consisting of (A) to (C) as a primer set as any DNA region selected from the group consisting of (1) to (3) above This is a region in the genomic DNA of the target konjac.

  The designed primer is then synthesized. Primers can be chemically synthesized according to the nucleotide sequence information. Methods for synthesizing oligonucleotides having an arbitrary base sequence are known. For example, the oligonucleotide can be synthesized by a DNA synthesizer. Specifically, DNA synthesizers based on principles such as the phosphoramidite method and the phosphonate method are now in practical use. These DNA synthesizers chemically link nucleotide monomers one by one on a solid phase according to a given base sequence. All reaction steps are automated, and synthesis is started by inputting target base sequence information. Therefore, the target DNA can be synthesized by giving the designed primer base sequence to such a DNA synthesizer.

  Subsequently, for each control konjac selected from Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, PCR is performed using the synthesized primer set with genomic DNA as a template. In the present invention, preferably, control konjac genomic DNA is first prepared (genomic DNA extraction). Genomic DNA can be prepared using, for example, control konjac leaves, roots, flowers, seeds, petioles, corms, suckers, calli, cultured cells, semen, etc., but is not particularly limited thereto. Extraction of genomic DNA from konjac or konjac cells is performed by methods generally known to those skilled in the art, such as the cetyltrimethylammonium bromide (CTAB) method (Murray and Thompson, Nucleic Acids Research 8, p.4321-4325, 1980). ) Etc. In addition, genomic DNA can be extracted using DNeasy (registered trademark) Plant Mini Kit (QIAGEN) or the like. Moreover, it is also possible to carry out PCR without using a genomic DNA extraction process, for example, directly using a cell disruption solution or the like.

  Examples of the PCR method include touchdown PCR method (Sato et al. 2005, DNA Res. 12, 301-364), nested PCR method (guideline for using PCR method, supervised by Yoshio Yazaki, Chugai Medical, 1998). However, the present invention is not limited to this, and those skilled in the art can implement the reaction conditions by appropriately selecting optimum conditions based on experiments or experience.

  Usually, PCR is performed using a commercially available reagent kit (rTaq, ExTaq, Takara; BIOTAQ, BIOLINE, etc.) containing a reaction solution and a thermostable polymerase, a commercially available PCR device (GeneAmp (registered trademark) PCR System 9700, ABI, etc.), etc. It can be carried out simply by using.

  Next, the presence or absence of the PCR product or the molecular size of the PCR product amplified by PCR is measured. Methods for measuring the presence or absence of a PCR product or the molecular size of a PCR product amplified by PCR include methods well known to those skilled in the art. Examples include, but are not limited to, a method using polyacrylamide gel electrophoresis, a method using agarose gel electrophoresis, a method using a fragment analyzer, and a microchip electrophoresis apparatus (Multina, Shimadzu).

  When measuring the molecular size of the PCR product, specifically, the PCR product is fluorescently labeled and then separated by capillary electrophoresis, and the molecular size of each PCR product separated is measured. Alternatively, PCR products are separated by electrophoresis (on polyacrylamide gel / agarose gel) and the molecular size of each separated PCR product is measured. Usually, the molecular size (for example, molecular weight or length) of each separated PCR product is measured using a DNA fragment (for example, a size marker) of a known size as a control. Next, the PCR products are classified by molecular size, and the kind of the PCR product is specified. The type of PCR product identified corresponds to a genotype specific for the control konjac.

  Next, a specific or specific genotype is identified among the control konjacs selected from Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari.

  Next, in the genomic DNA of the test konjac, the same DNA region showing a genotype specific to a specific or one control konjac among the control konjacs selected from Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari A genotype existing in the region (hereinafter referred to as “genotype in test konjac”) is identified. Identification of the genotype in the test konjac is preferably carried out by the same experimental method and experimental conditions as in the control konjac. Subsequently, the genotype specific to the control konjac is compared with the genotype in the test konjac by, for example, BioNumerics (distributor: Infocom, creator: Applied Maths).

The present invention also provides an invention comprising the step of detecting a genotype present in the DNA region (4) below.
(4) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a base sequence complementary to the base sequence described in SEQ ID NO: 8.
When detecting the genotype existing in the DNA region of (4) above, in addition to the steps of primer design, synthesis of the designed primer, PCR reaction using the designed primer, the DNA fragment obtained by the PCR reaction is used as a restriction enzyme HhaI. And the step of measuring the molecular size of the product obtained by the restriction enzyme treatment. Primer design, synthesis of the designed primer, PCR reaction, and measurement of molecular size can be performed by the methods described above. The type of restriction enzyme treatment product identified by measuring the molecular size corresponds to a genotype specific to the control konjac and the test konjac. Comparison of the genotype specific to the control konjac and the genotype in the test konjac can be performed by the method described above.

In the present invention, the genotype described in this example is exemplified as a genotype specific to any control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari. Yes, but not limited to this. For example, as a genotype specific to these control konjacs, the types of PCR products detected when PCR products amplified under PCR conditions different from those in this example are separated by the same separation method and conditions as in this example. Or the type of PCR product detected when a PCR product amplified under the same PCR conditions or different PCR conditions as in this example is separated by a different separation method and separation conditions from this example. The corresponding genotype may be used.
Further, a PCR product amplified under PCR conditions different from those in this example is decomposed under the same or different restriction enzyme treatment conditions as in this example, and the obtained restriction enzyme treatment products are separated in the same separation method and separation conditions as in this example. Or a genotype corresponding to the type of restriction enzyme treatment product detected when separated by different separation methods and separation conditions, or a PCR product amplified under the same PCR conditions as in this example, Restrictions detected when the product is decomposed under the same restriction enzyme treatment conditions or different restriction enzyme treatment conditions, and the obtained restriction enzyme treatment products are separated by the same separation method and separation conditions as in this example, or by different separation methods and separation conditions. It may be a genotype corresponding to the type of enzyme treatment product.

  Specific embodiments of the present invention include the following inventions (I) to (VII), and inventions arbitrarily combining (I) to (VII), but are not limited thereto. The invention includes all inventions that can be identified based on the results of the examples.

(I)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Miyama Sari, Kaki Odama or Miya Mama Sari is narrowed down as a candidate for the konjac varieties to be tested,
A method in which when the genotype described in (b) coincides with that of Harukuroro or Miyu Yutaka, the target of the tested konjac variety is narrowed down.
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 1 in the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence described in No. 2: a genotype specific to the control konjac, and (b) (a) in the genomic DNA of the test konjac Genotype of the same DNA region.

(II)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Ogaki Odama or Myougi Yutaka, Akao Odama or Myougi Yutaka is narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Harunakuro or Miyamakari, the candidate konjac variety is narrowed down to Harunakuro or Miyamakari;
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 3 in the genomic DNA of any konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 4, wherein the genotype is specific to the control konjac, and (b) in the genomic DNA of the test konjac (a ) Genotype of the same DNA region.

(III)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Harukuroro, Akao Odama or Harukuro is narrowed down as a candidate for the varieties of konjac.
When the genotype described in (b) matches that of Miyuki Yutaka, Miyu Yutaka was narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Miyama Sari, Miyama Sari is narrowed down as a candidate for the varieties of test konjac;
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 5 in the genomic DNA of any konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 6, wherein the genotype is specific to the control konjac, and (b) in the genomic DNA of the test konjac (a ) Genotype of the same DNA region.

(IV)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Akagi Odama, Akagi Odama is narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Harukuroro, Harukuro is narrowed down as a candidate for the varieties of konjac,
When the genotype described in (b) matches that of Miyuki Yutaka, Miyu Yutaka was narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Miyama Sari, Miyama Sari is narrowed down as a candidate for the varieties of test konjac;
(A) a genotype present in the DNA region described in (1) and (2) below in the genomic DNA of the control konjac, the genotype specific to the control konjac,
(B) the genotype of the same DNA region as (a) in the genomic DNA of the test konjac,
(1) a DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 1 and a base sequence complementary to the base sequence described in SEQ ID NO: 2;
(2) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a base sequence complementary to the base sequence described in SEQ ID NO: 4.

(V)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Akagi Odama, Akagi Odama is narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Harukuroro, Harukuro is narrowed down as a candidate for the varieties of konjac,
When the genotype described in (b) matches that of Miyuki Yutaka, Miyu Yutaka was narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Miyama Sari, Miyama Sari is narrowed down as a candidate for the varieties of test konjac;
(A) a genotype present in the DNA region described in (1) and (2) below in the genomic DNA of the control konjac, the genotype specific to the control konjac,
(B) the genotype of the same DNA region as (a) in the genomic DNA of the test konjac,
(1) a DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 1 and a base sequence complementary to the base sequence described in SEQ ID NO: 2;
(2) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 5 and a base sequence complementary to the base sequence described in SEQ ID NO: 6.

(VI)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Akagi Odama, Akagi Odama is narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Harukuroro, Harukuro is narrowed down as a candidate for the varieties of konjac,
When the genotype described in (b) matches that of Miyuki Yutaka, Miyu Yutaka was narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Miyama Sari, Miyama Sari is narrowed down as a candidate for the varieties of test konjac;
(A) a genotype present in the DNA region described in (1) and (2) below in the genomic DNA of the control konjac, the genotype specific to the control konjac,
(B) the genotype of the same DNA region as (a) in the genomic DNA of the test konjac,
(1) a DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a base sequence complementary to the base sequence described in SEQ ID NO: 4;
(2) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 5 and a base sequence complementary to the base sequence described in SEQ ID NO: 6.

(VII)
A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Miyama Sari, Kaki Odama or Miya Mama Sari is narrowed down as a candidate for the konjac varieties to be tested,
A method in which when the genotype described in (b) coincides with that of Harukuroro or Miyu Yutaka, the target of the tested konjac variety is narrowed down.
(A) a genotype specific to the control konjac in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and (ii) Genotype identified through the steps described in), and (b) genotype in the genomic DNA of the test konjac, (a) the genotype of the same DNA region as the control konjac,
(I) obtaining a DNA fragment comprising a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 8; And (ii) a step of degrading the DNA fragment obtained in step (a) with the restriction enzyme HhaI.

In addition, although the following can be illustrated as invention which combined (I)-(VII) arbitrarily, it is not limited to these.
-Invention combining (I) invention with (VI) invention-Invention combining (II) invention with (V) invention-Invention combining (III) invention with (IV) invention- An invention combining the invention of I) and the invention of (VII)-An invention combining the invention of (II) and the invention of (VII)-An invention combining the invention of (III) and the invention of (VII)-(IV) Inventions Combining Inventions of (VII) with Inventions of (V) and Inventions of (VII) Combining Inventions of (VI) and Inventions of (VII)

The present invention also provides a reagent for narrowing down konjac variety candidates and a kit for narrowing down konjac variety for use in the method of the present invention. Such reagents and kits include at least the following component (i).
(I) A set of oligonucleotides for amplifying by PCR any DNA region selected from the group consisting of (1) to (4) below (1) Complementary to the base sequence described in SEQ ID NO: 1 A DNA region sandwiched between a base sequence and a base sequence complementary to the base sequence described in SEQ ID NO: 2.
(2) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a base sequence complementary to the base sequence described in SEQ ID NO: 4.
(3) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 5 and a base sequence complementary to the base sequence described in SEQ ID NO: 6.
(4) A DNA region sandwiched between a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a base sequence complementary to the base sequence described in SEQ ID NO: 8.

Examples of oligonucleotide sets for amplifying the DNA regions (1) to (4) above by PCR include the following sets (A) to (D), but are not limited thereto.
(A) A set of oligonucleotides containing the base sequence set forth in SEQ ID NO: 1 and oligonucleotides containing the base sequence set forth in SEQ ID NO: 2.
(B) A set of oligonucleotides containing the base sequence set forth in SEQ ID NO: 3 and oligonucleotides containing the base sequence set forth in SEQ ID NO: 4.
(C) An oligonucleotide set comprising the base sequence set forth in SEQ ID NO: 5 and an oligonucleotide set comprising the base sequence set forth in SEQ ID NO: 6.
(D) An oligonucleotide set comprising the base sequence set forth in SEQ ID NO: 7 and an oligonucleotide set comprising the base sequence set forth in SEQ ID NO: 8.

In addition to the component (i), the reagent or kit of the present invention may include the component (ii).
(Ii) Restriction enzyme HhaI
In particular, when the reagent or kit of the present invention contains an oligonucleotide set for amplifying the DNA region (4) by PCR, the reagent or kit preferably further contains a restriction enzyme HhaI.

In addition to the components (i) and (ii), the reagents and kits can further include the following additional elements (iii) or (iv).
(Iii) DNA polymerase: The reagent or kit of the present invention may contain a DNA polymerase that catalyzes a template-dependent complementary strand synthesis reaction. Various DNA polymerases used in known nucleic acid synthesis reactions such as PCR can be used in the present invention.
(Iv) Nucleotide substrate: The reagent or kit of the present invention may contain nucleotides used as a substrate for a complementary strand synthesis reaction of a nucleic acid. Specifically, at least one of dCTP, dGTP, dTPT, and dATP, usually all of these (dNTP) can be included in the kit. These nucleotides can utilize not only natural structures but also derivatives. Nucleotides modified with fluorescent substances or binding ligands are known. The above-mentioned reagents and kits can be accompanied by a document that describes the presence or absence of an amplification product by PCR and the size of the PCR product amplified by PCR. Moreover, the size information of the PCR product amplified by PCR can be converted into machine-readable data and added to a reagent or kit as a recording medium storing the data.

  For example, as a reagent or a kit used for determining whether Akagi Odama or Miyayama Masari is narrowed down as a candidate for the konjac variety to be tested, or whether Harukuroro or Miyagi Yutaka is narrowed down, (A ) To (D), or a reagent or kit containing at least the set described in (A), or a reagent or kit containing at least the set described in (D) and the restriction enzyme HhaI.

  For example, as a reagent or kit used to determine whether kurokuro or Miyayamasari is narrowed down as a candidate for the konjac varieties to be tested, or whether Akagi Odama or Myogi Yutaka is narrowed down, (A ) To (D), and a reagent or kit including at least the set described in (B) can be exemplified.

  For example, as a reagent or a kit used to determine whether Akagi Odama or Harukuroro is narrowed down as a candidate for the konjac varieties to be tested, Ayumi Yutaka is narrowed down, or Miyamakari is narrowed down, Examples thereof include reagents and kits including at least the set described in (C) selected from the group consisting of (A) to (D).

  For example, reagents and kits used to determine whether Akagi Odama is narrowed down as a candidate for the konjac varieties to be tested, whether Harukuro is narrowed down, Yugi Yutaka is narrowed down, or Miyamayakari is narrowed down As a reagent or kit containing at least the set of (A) and (B) selected from the group consisting of (A) to (D) above, a reagent or kit containing at least the set of (A) and (C), Reagents and kits containing at least the set of (B) and (C), at least sets of (A) and (D) and a reagent and kit containing the restriction enzyme HhaI, at least the sets of (B) and (D) and the restriction enzyme HhaI And a reagent or kit containing at least the set of (C) and (D) and the restriction enzyme HhaI.

Furthermore, the present invention provides a template of any of the control konjac genomic DNA selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, from the group consisting of (A) to (D) above. A PCR product that is amplified by PCR using any selected set as a primer set is provided. The present invention also provides PCR using as a template the genomic DNA of any control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari, and using the above set (D) as a primer set. The product obtained by digesting the PCR product amplified by the restriction enzyme HhaI is provided. As such a PCR product or a degradation product of HhaI, for example, an oligonucleotide containing a base sequence described in any of SEQ ID NOs: 10 to 12, 14, 18 to 21, or a base sequence complementary to the base sequence is included. Can be mentioned. The method for producing and using the PCR product and the degradation product of HhaI are as described above.
The degradation product of HhaI has a protruding end. Therefore, one strand of the double-stranded DNA (for example, the base sequence described in SEQ ID NO: 18 or 19) is complementary to the complementary strand (for example, the base sequence complementary to the base sequence described in SEQ ID NO: 18, 19). It is not perfectly complementary (since double-stranded DNA with protruding ends does not form base pairs at the ends). Even if one strand of the double-stranded DNA and its complementary strand are not completely complementary because of this reason or because the sequence of the PCR product is heterogeneous, the present invention Is included in the meaning of “complementary”.

  EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, this invention is not restrict | limited to these Examples.

[Example 1] Identification of konjac varieties using kon601
(1) Extraction of konjac genomic DNA Five varieties and strains of konjac corms including the main cultivars “Akagi Odama”, “Harunuro”, “Myogi Yutaka”, “Miyama Sari” and one other line (a Chinese species) And DNA was extracted from the sample. Freezing and grinding the above 5 varieties / lines of corm buds in liquid nitrogen, and adding 0.1 mg of polyvinylpyrrolidone (PVP) and 20 mg of sodium dodecyl sulfate (SDS) to the ground tissue, 0.8 ml cetyl trimethyl ammonium Suspended with bromide (CTAB) extract. The composition of the extract at this time was 1% CTAB, 0.1 M Tris-HCl (pH 8.0), 50 mM ethylene diamine tetraacetic acid (EDTA), 1.4 M sodium chloride (NaCl), 0.1% β-mercaptoethanol (CTAB method) Met. Add 40 μg of proteinase K (MERCK) to the lysate and let stand at 56 ° C for 30 minutes, then treat with PCI (Phenol / Chloroform / Isoamylalchohol (25: 24: 1)), CIA (Chloroform / Isoamylalchohol (24: 1)) And the supernatant was collected. Subsequently, the genomic DNA of varieties and strains of konjac was extracted by purification by isopropyl alcohol precipitation.

(2) PCR reaction PCR was performed using 2 ng of extracted genomic DNA as a template.
The reagent composition of the PCR is 1 ng TaKaRa Ex Taq HS (Takara Bio Inc.), 2 μl of 10 × Ex Taq Buffer, 5 nmol of dNTP Mixture, variety identification primers kon601-F and kon601-R (SEQ ID NO :) 1 and 2) The reaction was started by preparing 20 μl in total (0.75 pmol) 1.5 μl and 20 μl of sterilized water respectively in a PCR tube.
The PCR reaction was performed using iCycler (manufactured by BIO RAD) at 95 ° C for 10 minutes, followed by 36 cycles of 95 ° C for 15 seconds, 67 ° C for 10 seconds, and 72 ° C for 5 seconds.

(3) Analysis of amplified fragment length using agarose gel electrophoresis Add 4 μl of 6 × loading buffer to 20 μl of amplification product obtained after reaction, and add 3 in 0.5 × TBE (50 mM Tris, 62 mM Boric acid, 1 mM EDTA). Electrophoresis was performed on a% agarose gel. As the electrophoresis apparatus, Mupid II (manufactured by Cosmo Bio) was used. The agarose gel after electrophoresis was immersed in ethidium bromide solution for staining, and after decolorization, a band was detected under ultraviolet irradiation. Photographs were taken to compare polymorphisms between varieties and strains (Fig. 1). The detection results are summarized in Table 1 (identification of varieties by kon601 marker).

  A DNA fragment obtained by a PCR reaction using Miyama Sari genomic DNA as a template and an oligonucleotide containing the nucleotide sequence of SEQ ID NOs: 1 and 2 as a primer is shown in SEQ ID NO: 10.

[Example 2] kon603-F and kon603-R (SEQ ID NOS: 3 and 4) were used as varietal identification primers for konjac varieties using kon603. After the reaction, the konjac cultivar / line was identified in the same manner as in Example 1 except that the reaction at 95 ° C. for 15 seconds, 65 ° C. for 10 seconds, and 72 ° C. for 2 seconds was repeated for 38 cycles. The results are shown in FIG. 2 and Table 2 (variety identification by kon603 marker). The symbols in the table are the same as those in Table 2.

  The base sequence of the DNA fragment obtained by PCR reaction using the genomic DNA of Akagi Odama and Myougi Yutaka as a template and the oligonucleotide containing the base sequence described in SEQ ID NOs: 3 and 4 as a primer is shown in SEQ ID NO: 11. Show.

[Example 3] Identification of konjac cultivars using kon272 cultivar identification primer kon272 Using 20 ng of extracted genomic DNA, using kon272-F and kon272-R (SEQ ID NOs: 5 and 6) as cultivar identification primers, PCR The konjac cultivar was the same as in Example 1 except that the reaction was carried out at 95 ° C for 10 minutes and then repeated at 95 ° C for 15 seconds, 55 ° C for 30 seconds, and 72 ° C for 10 seconds for 30 cycles. System identification was performed. The results are shown in FIG. 3 and Table 3 (variety identification by kon272 marker). In the table, “C1”, “C2”, “C3”, “C4”, and “C5” represent different chain lengths (sizes) of the amplified DNA fragments. Other symbols are the same as in Table 2.

The base sequence of the DNA fragment obtained by PCR reaction using the genomic DNA of Akagi Odama as a template and the oligonucleotide containing the base sequence described in SEQ ID NOs: 5 and 6 as the primer, SEQ ID NO: 12 (band name C4) Shown in
The base sequence of the DNA fragment obtained by PCR reaction using the genomic DNA of Akagi Odama as a template and the oligonucleotide containing the base sequence described in SEQ ID NO: 5 and 6 as a primer, SEQ ID NO: 20 (band name C2) Shown in
The base sequence of a DNA fragment obtained by PCR reaction using the genomic DNA of Myogyu Yutaka as a template and the oligonucleotide containing the base sequence described in SEQ ID NOs: 5 and 6 as a primer, SEQ ID NO: 14 (band name C3) Shown in

[Example 4] Identification of konjac varieties using cultivar identification primer kon601-CAPS
(1) Extraction of konjac genomic DNA Five varieties and strains of konjac corms including the main cultivars “Akagi Odama”, “Harunuro”, “Myogi Yutaka”, “Miyama Sari” and one other line (a Chinese species) And DNA was extracted from the sample. Freezing and grinding the above 5 varieties / lines of corm buds in liquid nitrogen, and adding 0.1 mg of polyvinylpyrrolidone (PVP) and 20 mg of sodium dodecyl sulfate (SDS) to the ground tissue, 0.8 ml cetyl trimethyl ammonium Suspended with bromide (CTAB) extract. The composition of the extract at this time was 1% CTAB, 0.1 M Tris-HCl (pH 8.0), 50 mM ethylene diamine tetraacetic acid (EDTA), 1.4 M sodium chloride (NaCl), 0.1% β-mercaptoethanol (CTAB method) Met. Add 40 μg of proteinase K (MERCK) to the lysate and let stand at 56 ° C for 30 minutes, then treat with PCI (Phenol / Chloroform / Isoamylalchohol (25: 24: 1)), CIA (Chloroform / Isoamylalchohol (24: 1)) And the supernatant was collected. Subsequently, the genomic DNA of varieties and strains of konjac was extracted by purification by isopropyl alcohol precipitation.

(2) PCR reaction PCR was performed using 20 ng of extracted genomic DNA as a template.
PCR reagent composition is 20 ng of extracted DNA, 1 Units TaKaRa Ex Taq HS (Takara Bio Inc.), 2 μl of 10 × Ex Taq Buffer, 5 nmol of dNTP Mixture, breed identification primers kon601CAPS-F and kon601CAPS-R (SEQ ID NO: 7 and 8) 1.5 μl each (0.75 pmol) and a total of 20 μl with sterilized water added were prepared in PCR tubes to start the reaction.
The PCR reaction was carried out using iCycler (manufactured by BIO RAD) at 95 ° C for 10 minutes, followed by 35 cycles of 95 ° C for 15 seconds, 65 ° C for 30 seconds, and 72 ° C for 30 seconds.

(3) The amplification product obtained after the DNA digestion reaction with the restriction enzyme HhaI was digested with the restriction enzyme HhaI.
For restriction enzyme digestion, prepare 10 μl of the amplified product, 4Units HhaI (NEB), 4 μl of 10 × NEBuffer 4, 0.4 μl of 100 × BSA, 25.4 μl of sterilized water for a total of 40 μl in a 0.5 ml tube. And reacted at 37 ° C. for 2 hours.

(4) Analysis of cleavage amplification polymorphism using agarose gel electrophoresis Add 6 μl loading buffer 1.6 μl to the digested product 8 μl after the reaction, then add 0.5 μTBE (50 mM Tris, 62 mM Boric acid, 1 mM EDTA), 3 Electrophoresis was performed on a% agarose gel. As the electrophoresis apparatus, Mupid II (manufactured by Cosmo Bio) was used. The agarose gel after electrophoresis was immersed in ethidium bromide solution for staining, and after decolorization, a band was detected under ultraviolet irradiation. Photographs were taken to compare polymorphisms between varieties and strains (Fig. 4). The detection results are summarized in Table 4.

The base sequence of a DNA fragment obtained by PCR reaction using Harukuroro genomic DNA as a template and an oligonucleotide containing the base sequences described in SEQ ID NOs: 7 and 8 as primers is shown in SEQ ID NO: 21.
The base of the DNA fragment obtained as a result of digesting the DNA fragment obtained by PCR reaction using the genomic DNA of Harunokuro as a template and the oligonucleotide containing the nucleotide sequence of SEQ ID NOs: 7 and 8 as a primer with the restriction enzyme HhaI The sequence is shown in SEQ ID NO: 18 (band name 223) and 19 (band name 130).
The band names shown in Table 4 were named based on the length of one strand of the double-stranded DNA. Since the degradation product of HhaI has a protruding end, the strand length may differ between one strand of the double-stranded DNA and its complementary strand. It is not excluded.

Claims (14)

A method for narrowing down candidates for varieties of test konjac including the step of comparing the genotype described in (a) below and the genotype described in (b) below, wherein the genotypes compared in the step match In this method, the varieties of the control konjac are selected as candidates for the varieties of the test konjac, and the genotype in the genomic DNA of the control konjac is at least one selected from the group consisting of (1) to (3) below. A method that is a genotype of a DNA region;
(A) a genotype in the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Miyugi Yutaka, and Miyama Sari, wherein the genotype is specific to the control konjac, and (b) Genotype of the same DNA region as in (a) in the genomic DNA of konjac (1) Base sequence complementary to the base sequence described in SEQ ID NO: 1, and complementary to the base sequence described in SEQ ID NO: 2 DNA region sandwiched between base sequences,
(2) a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 4; and (3) SEQ ID NO: 5 And a DNA region sandwiched between a base sequence complementary to the base sequence described in [5] and a base sequence complementary to the base sequence described in SEQ ID NO: 6. The method according to claim 1, wherein the genotype in the genomic DNA of the control konjac is the genotype of the DNA region described in (1) and (2) below;
(1) a base sequence complementary to the base sequence described in SEQ ID NO: 1, and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 2; and (2) SEQ ID NO: 3 And a DNA region sandwiched between a base sequence complementary to the base sequence described in 1 and a base sequence complementary to the base sequence described in SEQ ID NO: 4. The method according to claim 1, wherein the genotype in the genomic DNA of the control konjac is the genotype of the DNA region described in (1) and (2) below;
(1) a base sequence complementary to the base sequence described in SEQ ID NO: 1, and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 2; and (2) SEQ ID NO: 5 And a DNA region sandwiched between a base sequence complementary to the base sequence described in [5] and a base sequence complementary to the base sequence described in SEQ ID NO: 6. The method according to claim 1, wherein the genotype in the genomic DNA of the control konjac is the genotype of the DNA region described in (1) and (2) below;
(1) a base sequence complementary to the base sequence described in SEQ ID NO: 3 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 4; and (2) SEQ ID NO: 5 And a DNA region sandwiched between a base sequence complementary to the base sequence described in [5] and a base sequence complementary to the base sequence described in SEQ ID NO: 6. A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Miyama Sari, Kaki Odama or Miya Mama Sari is narrowed down as a candidate for the konjac varieties to be tested,
A method in which when the genotype described in (b) coincides with that of Harukuroro or Miyu Yutaka, the target of the tested konjac variety is narrowed down.
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 1 in the genomic DNA of a control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence described in No. 2: a genotype specific to the control konjac, and (b) (a) in the genomic DNA of the test konjac Genotype of the same DNA region. A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Ogaki Odama or Myougi Yutaka, Akao Odama or Myougi Yutaka is narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Harunakuro or Miyamakari, the candidate konjac variety is narrowed down to Harunakuro or Miyamakari;
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 3 in the genomic DNA of any konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 4, wherein the genotype is specific to the control konjac, and (b) in the genomic DNA of the test konjac (a ) Genotype of the same DNA region. A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Harukuroro, Akao Odama or Harukuro is narrowed down as a candidate for the varieties of konjac.
When the genotype described in (b) matches that of Miyuki Yutaka, Miyu Yutaka was narrowed down as a candidate for the konjac cultivar,
When the genotype described in (b) matches that of Miyama Sari, Miyama Sari is narrowed down as a candidate for the varieties of test konjac;
(A) a base sequence complementary to the base sequence set forth in SEQ ID NO: 5 in the genomic DNA of any konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari; A genotype of a DNA region sandwiched by a base sequence complementary to the base sequence set forth in SEQ ID NO: 6, wherein the genotype is specific to the control konjac, and (b) in the genomic DNA of the test konjac (a ) Genotype of the same DNA region. A method for narrowing down candidates for the varieties of test konjac including a step of comparing the genotype described in (a) below and the genotype described in (b) below,
When the genotype described in (b) matches that of Kagi Odama or Miyama Sari, Kaki Odama or Miya Mama Sari is narrowed down as a candidate for the konjac varieties to be tested,
A method in which when the genotype described in (b) coincides with that of Harukuroro or Miyu Yutaka, the target of the tested konjac variety is narrowed down.
(A) a genotype specific to the control konjac in the genomic DNA of the control konjac selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari, and at least the following (i) and (ii) Genotype identified through the steps described in), and (b) genotype in the genomic DNA of the test konjac, (a) the genotype of the same DNA region as the control konjac,
(I) obtaining a DNA fragment comprising a base sequence complementary to the base sequence described in SEQ ID NO: 7 and a DNA region sandwiched between base sequences complementary to the base sequence described in SEQ ID NO: 8; And (ii) a step of degrading the DNA fragment obtained in step (i) with the restriction enzyme HhaI. At least one set selected from the group consisting of (A) to (D) below;
(A) an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 1 and a set of oligonucleotides consisting of the base sequence set forth in SEQ ID NO: 2,
(B) an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 3 and a set of oligonucleotides consisting of the base sequence set forth in SEQ ID NO: 4,
(C) an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 5 and a set of oligonucleotides consisting of the base sequence set forth in SEQ ID NO: 6; and (D) consisting of the base sequence set forth in SEQ ID NO: 7. A set of oligonucleotides and an oligonucleotide consisting of the nucleotide sequence set forth in SEQ ID NO: 8. A kit for narrowing down konjac variety candidates containing the set according to claim 9. The kit according to claim 10, further comprising a restriction enzyme HhaI. Among the konjac varieties, at least one selected from the group consisting of the following (i) to (iv), using as a template a konjac genomic DNA selected from the group consisting of Akagi Odama, Harukuroro, Myougi Yutaka, and Miyama Sari A method for producing a DNA fragment , comprising the step of amplifying the DNA fragment by PCR using one set as a primer set;
(I) an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 1 and a set of oligonucleotides consisting of the base sequence set forth in SEQ ID NO: 2;
(Ii) a set of oligonucleotides consisting of the base sequence set forth in SEQ ID NO: 3 and an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 4;
(Iii) an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 5 and a set of oligonucleotides consisting of the base sequence set forth in SEQ ID NO: 6; and (iv) consisting of the base sequence set forth in SEQ ID NO: 7. A set of oligonucleotides and an oligonucleotide consisting of the nucleotide sequence set forth in SEQ ID NO: 8. A method for producing a DNA fragment , comprising the steps described in (a) and (b) below;
(A) an oligonucleotide consisting of the base sequence set forth in SEQ ID NO: 7, using as a template a konjac genomic DNA selected from the group consisting of konjac varieties Akagi Odama, Harunuro, Miyugi Yutaka, and Miyama Sari; And a step of amplifying a DNA fragment by PCR using a set of oligonucleotides comprising the nucleotide sequence set forth in SEQ ID NO: 8 as a primer set, and (b) the DNA fragment obtained in step (a) is digested with the restriction enzyme HhaI. The process of disassembling. DNA consisting of the base sequence described in any of SEQ ID NOs: 10-12, 14, 18-21 or a base sequence complementary to the base sequence.