CN108977551A - One kind SNP marker relevant to Macrobrachium rosenbergii body ruler and growth traits and its application - Google Patents
One kind SNP marker relevant to Macrobrachium rosenbergii body ruler and growth traits and its application Download PDFInfo
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Abstract
The invention discloses one kind SNP markers relevant to Macrobrachium rosenbergii body ruler and growth traits and its application that belong to molecular marker breeding technical field.The SNP marker corresponds to the site Macrobrachium rosenbergii ND1 Gene A 571-, and base is A or C herein.SNP marker and Macrobrachium rosenbergii body ruler (body length of the invention, eye socket away from, periproct is wide, carapace is high, promerous is high) and growth (pH value of meat) character correlation, it is a new molecular labeling, by the genotype of determination Macrobrachium rosenbergii SNP site to be measured to the body ruler (body length to Macrobrachium rosenbergii, eye socket away from, periproct is wide, carapace is high, promerous is high) and growth (pH value of meat) character progress early stage breeding, production cost can effectively be saved and accelerate genetic progress, preferably serve the breeding of Macrobrachium rosenbergii, both it had been able to satisfy the huge market demand, again with very big Economic Application value and scientific research value.
Description
Technical field
The invention belongs to molecular marker breeding technical fields, in particular to one kind and Macrobrachium rosenbergii body ruler and growth traits phase
The SNP marker and its application of pass.
Background technique
Molecular mark (Marker Assisted Selection, MAS) is using molecular labeling and to determine mesh
The characteristics of marking the gene close linkage of character is screened and important economic characters (such as weight, growth in animals and plants breeding process
Speed, resistance etc.) relevant molecular labeling, and building has the breeding population of related molecular marker in breeding process, with
Achieve the purpose that a kind of breeding method of selection target character, accuracy high feature strong with Objective can be significantly
Breeding efficiency is improved, the breeding time limit is shortened.
Mononucleotide loci polymorphism (Single Nucleotide Polymorphisms, SNP) is on genome by list
The nucleotide variation that a nucleotide generates has the characteristics that distributed quantity is more, rich polymorphism, be after microsatellite molecular marker it
Another important molecular genetic marker, referred to as third generation molecular genetic marker afterwards.The label is widely used to animals and plants mark
Remember the fields such as assistant breeding, the assignment of genes gene mapping, genetic diversity Journal of Sex Research.
ND1 gene is the gene for encoding nadh dehydrogenase subunit 1,1 (NADH of nadh dehydrogenase subunit
Dehydrogenase subunit 1, ND1) gene be mtDNA protein coding gene, including cytochrome b, cytochromes
The coded sequence of 7 subunits of 3 subunits of oxidizing ferment, 2 subunits of ATP enzyme and nadh dehydrogenase is responsible for the egg of coding
White is the subunit I of nadh dehydrogenase.Nadh dehydrogenase is the main composition of electron transport chain complex I, by direct in respiratory chain
It participates in hydrogen and electron transmission and goes to participate in energetic supersession effect by oxidative phosphorylation generation ATP.Thus, it influences to a certain extent
The acquisition of animal exogenous nutrition substance, assimilation utilize and the activity of the vital metabolics such as transhipment and then the character of animal risen decisive
Effect.It is more about species ND1 gene diversity Journal of Sex Research both at home and abroad, such as three tail swallowtail butterflies (Bhutanitis thaidina), nothing
The discussion of the phylogeographies and genetic development such as web gecko (Gekko swinhonis), tree toad (Hylid).Currently, Hou Lingling
Have found chicken NDl Gene A 4589G mutation and caecum length, 8 week old chest depths, 8 week old keel lengths and 8 week old shins length, leg flesh length
There is significant correlation respectively with the influence of leg flesh width, glucose, lactic dehydrogenase, abdominal fat, abdominal fat and subcutaneous fat thickness.
Macrobrachium rosenbergii, also known as Malaysian prawn, fresh water prawn, big long-armed prawn are under the jurisdiction of Arthropoda, hapalonychia
Guiding principle, Decapoda, Palaemonidae, pond crayfish category are one of tropical fresh water shrimps largest in the world, and with growing, fast, feeding habits are wide, resistance to
The features such as high temperature, premunition are strong, the culture-cycle is short, mouthfeel is fresh and tender and rich in nutrition content and by consumers.It originates in
In the India Pacific region, various types of fresh water or salt-fresh water waters are lived in, is supported later by the shifting of many countries and regions numerous
It grows, becomes local main freshwater aquiculture shrimps.Currently, Macrobrachium rosenbergii is up to more than 60 ten thousand mu, but Roche in the cultured area of China
The breeding quantity of pond crayfish is far from meeting its huge industry size and huge seed demand, therefore, the early stage of Macrobrachium rosenbergii
Breeding seems very urgent and significant.
Summary of the invention
To overcome the above insufficient or defect in the prior art, the present invention provides a kind of and Macrobrachium rosenbergii body ruler and growths
The relevant SNP marker of character and its application, can be by the genotype of determination Macrobrachium rosenbergii SNP site to be measured to Roche
Pond crayfish body ruler (body length, eye socket away from, periproct is wide, carapace is high, promerous is high) and growth (pH value of meat) character
Early stage breeding is carried out, is limited without age, the gender etc. by Macrobrachium rosenbergii, be can be effectively used for the early stage breeding of Macrobrachium rosenbergii, promote
Into the breeding process of Macrobrachium rosenbergii.
The technical solution used in the present invention is:
A kind of SNP marker relevant to Macrobrachium rosenbergii body ruler and growth traits, the SNP marker are located at Roche
The site pond crayfish ND1 Gene A 571-, base is A or C herein.
Application of the SNP marker in Macrobrachium rosenbergii early stage breeding.
A kind of Macrobrachium rosenbergii body ruler and the method for growth traits early stage breeding, for according to Macrobrachium rosenbergii ND1 Gene A 571-
The genotype of point carries out early stage breeding to Macrobrachium rosenbergii body ruler and growth traits, includes the following steps:
(1) design specific amplification contains the primer pair of the genetic fragment in the site Macrobrachium rosenbergii ND1 Gene A 571-；
(2) genomic DNA of Macrobrachium rosenbergii to be measured is extracted；
(3) PCR amplification, detection amplification gained are carried out with genomic DNA of step (1) the resulting primer pair to Macrobrachium rosenbergii
The genotype of the SNP site of genetic fragment；
(4) early stage breeding is carried out to Macrobrachium rosenbergii body ruler and growth traits based on the genotype of SNP site.
As a further improvement of the foregoing solution, the primer sequence of the PCR amplification is
ND1-F:5 '-GATAAAGTAGGCTATGCTGG-3 ' (SEQ ID № 1),
ND1-R:3 '-CCTCCTCTGTACTCGGTATT-5 ' (SEQ ID № 2).
As a further improvement of the foregoing solution, the amplification instrument that the PCR amplification uses is BIO-RAD T100PCR instrument.
The beneficial effects of the present invention are: the present invention provides a kind of SNPs relevant to Macrobrachium rosenbergii body ruler and growth traits
Molecular labeling and its application, the SNP marker are located at the site Macrobrachium rosenbergii ND1 Gene A 571-, and base is A or C herein.
Body ruler and growth of the nucleotide sequence of ND1 gene from 5 ' end 571 bit base A or C and Macrobrachium rosenbergii in the Macrobrachium rosenbergii
The significant correlation of shape, i.e. SNP marker on the site Macrobrachium rosenbergii ND1 Gene A 571- and Macrobrachium rosenbergii body ruler (body length,
Eye socket away from, periproct is wide, carapace is high, promerous is high) and growth (pH value of meat) character it is related, be a new molecule mark
Note, by the genotype of determination Macrobrachium rosenbergii SNP site to be measured to which (body length, eye socket are away from, periproct to Macrobrachium rosenbergii body ruler
Wide, carapace height, promerous are high) and growth (pH value of meat) character progress early stage breeding, it can effectively save production cost
And accelerate genetic progress, the early stage breeding of Macrobrachium rosenbergii is preferably served, had not only been able to satisfy the huge market demand, but also have very
Big Economic Application value and scientific research value.
Detailed description of the invention
Fig. 1 is the PCR products electrophoresis map of Macrobrachium rosenbergii ND1 Gene Partial segment；
Fig. 2 is 571 mutational site genotype mutations sequence alignment of Macrobrachium rosenbergii ND1 gene.
Specific embodiment
The present invention is specifically described below with reference to embodiment, in order to technical field personnel to of the invention
Understand.It is necessary to it is emphasized that embodiment is only intended to, the present invention will be further described herein, should not be understood as to this
The limitation of invention protection scope, fields person skilled in the art, according to foregoing invention content non-to made by the present invention
The modifications and adaptations of matter should still fall within protection scope of the present invention.Mentioned raw materials following simultaneously are unspecified,
For commercial product；The processing step or preparation method not referred in detail be processing step known to a person skilled in the art
Or preparation method.
The source of the Macrobrachium rosenbergii cultured population of test: Guangdong (GD) adopts 47 samples；Adopt 76 samples in Guangxi 1 (GX1)
Product；Adopt 35 samples in Guangxi 2 (GX2)；44 samples are adopted in Hainan (HN), are provided by the seedling base of three water-white golden breeding companies,
Raised under identical environmental condition 106, in July, 2017 random acquisition at shrimp.
Embodiment 1
One, the detection of SNP marker
1. design primer: design specific amplification contains the primer of the genetic fragment in the site Macrobrachium rosenbergii ND1 Gene A 571-
It is right.
Using software Primer 5.0, with the ND1 gene (GenBank:NC_006880.1) of Macrobrachium rosenbergii in GenBank
The specificity amplification primer for making Reference Design, the primer sequence expanded are
Upstream F:5 '-GATAAAGTAGGCTATGCTGG-3 ' (SEQ ID № 1), 20bp；
Downstream R:3 '-CCTCCTCTGTACTCGGTATT-5 ' (SEQ ID № 2), 20bp.
Optimum temperature is 48.8 DEG C, product length 542bp, and by Guangzhou, Sheng Gong bioengineering Co., Ltd is synthesized.
2. the extraction of Macrobrachium rosenbergii genomic DNA
Use the whole blood kit of OMEGAD, the specific steps are as follows:
(1) each sample takes the blood sample of 150 μ L, and buffer Elution Buffer is added, and vortex mixes 10s；
(2) the Buffer GL lysate of 500 μ L is added in each sample, shakes up 20s manually, stands 20min；
(3) after the GL2 lysate of 100 μ L is added, there is white opacity in solution, after vortex mixes 60s, 13000 × g high speed
It is centrifuged 15min, the phenomenon that separation of solid and liquid after centrifugation；
(4) supernatant after centrifugation is transferred in adsorption column, 10000 × g high speed centrifugation 1min, is outwelled in absorption column tube
Waste liquid；
(5) the HB Buffer that 500 μ L are added binds liquid, after 10000 × g is centrifuged 1min, outwells useless in absorption column tube
Liquid；
(6) the Wash Buffer cleaning solution of 650 μ L is added, 10000 × g high speed centrifugation 1min is outwelled in absorption column tube
Waste liquid；
(7) (6) step is repeated；
(8) the Elution Buffer dilution of 70 DEG C of preheatings is added, 1000 × g is centrifuged after being incubated at room temperature 3min；
(9) liquid that centrifugation is obtained rejoins in adsorption column, and 1000 × g is centrifuged after being incubated at room temperature 3min, carries out pair
The label answered, -20 DEG C of preservations.
3. amplification and detection: carrying out PCR amplification, detection amplification with genomic DNA of the primer pair of design to Macrobrachium rosenbergii
The genotype of the SNP site of gained genetic fragment.
Take 40 samples at random in the genome extracted, every 4 samples take 2 μ L to mix, are divided into 10 groups, carry out PCR respectively
Amplification amounts to 10 samples.
Program: the PCR SuperMix of full formula gold is used.
System: DD H2O:22 μ L；Mix:25 μ L；
Upstream primer: 1 μ L；Downstream primer: 1 μ L；DNA:1 μ L.
Using BIO-RAD T100PCR instrument, wherein program setting: A, 94 DEG C of initial denaturation 5min；B, 94 DEG C of denaturation 30s；C,
48.8 DEG C of annealing 30s；D, 72 DEG C of extension 1min；E, B~D30 circulation；F:72 DEG C of extension 5min；G:4 DEG C of constant temperature saves.
With 0.8g BIOWEST agarose, 1.0% agarose is made in 1 × TAE liquid of 80ml and 8 μ L Goldview
It is solidifying.With 5 μ L product point samples, using the full formula gold DNA Marker DL2000 of 5 μ L as reference, in BIO-RAD Powerpac electrophoresis
In instrument, use 1 × TAE liquid as room temperature electrophoresis.(wherein, voltage: 150V；Electric current 400mA；Time: 20min.) after electrophoresis,
It observes and photographs to record under Tanon gel imaging system.Determine single and clearly bright purpose band occur (such as Fig. 1 institute
Show) after send to Guangzhou Sheng Gong biotech firm and be sequenced, Genotyping is carried out according to sequencing result, obtains Fig. 2.
Two, the association analysis of SNP site genotype and character
The relevance of linear analogue analysis SNP site genotype and character is carried out using SAS9.0 software Mixed program,
In, when analysis with body ruler (body length, eye socket away from, periproct is wide, carapace is high, promerous is high) and growth (pH value of meat)
Character represents phenotypic number, as follows using model:
Model: Yijkx=p+Bj+Gk+Eijkl+Fx+bjk:
YijkxFor the observation of Carcass Traits, p is group's mean, BjIt is sex-effects, GkFor genotype effects.
EijklFor random error.FxFor family stochastic effects.bjkFor the regression coefficient for influencing slaughter traits.With GLM program
The least squares means and standard error of different genotype slaughter trait are calculated, while carrying out significance test.
The gene frequency and body ruler and the association analysis of growth traits of its SNP site are as shown in table 1 below.
The gene frequency of 1 SNP site of table and the association analysis of body ruler and growth traits
As shown in Table 1, the SNP site be the body length of Macrobrachium rosenbergii of homozygous deletion, eye socket away from, periproct wide, cephalothorax
First is high, promerous height is significantly higher than AA type (P < 0.05), and the pH value of meat is noticeably greater than AA type (P < 0.01).The nucleotide
Sequence from 5 ' end 571 bit base A or C and Macrobrachium rosenbergii body ruler (body length, eye socket away from, periproct is wide, carapace is high, first
Uromere is high) and the growth significant correlation of (pH value of meat) character.
Above-described embodiment is the preferred embodiment of the present invention, all with similar technique of the invention and made equivalence changes,
It should belong to protection category of the invention.
SEQUENCE LISTING
<110>Foshan Science &. Technology College
<120>a kind of SNP marker relevant to Macrobrachium rosenbergii body ruler and growth traits and its application
<130> 2018.08.01
<160> 2
<170> PatentIn version 3.5
<210> 1
<211> 20
<212> DNA
<213>artificial sequence
<400> 1
gataaagtag gctatgctgg 20
<210> 2
<211> 20
<212> DNA
<213>artificial sequence
<400> 2
cctcctctgt actcggtatt 20
Claims (6)
1. a kind of SNP marker relevant to Macrobrachium rosenbergii body ruler and growth traits, which is characterized in that the SNP molecule mark
Note is located at the site Macrobrachium rosenbergii ND1 Gene A 571-, and base is A or C herein.
2. a kind of application of SNP marker relevant to Macrobrachium rosenbergii body ruler and growth traits, which is characterized in that right
SNP marker described in asking 1 is applied in Macrobrachium rosenbergii early stage breeding.
3. a kind of Macrobrachium rosenbergii body ruler and the method for growth traits early stage breeding, which is characterized in that according to claim 1
The genotype of SNP site carries out early stage breeding to Macrobrachium rosenbergii body ruler and growth traits.
4. according to the method described in claim 3, it is characterized by comprising the following steps:
(1) design specific amplification contains the primer pair of the genetic fragment in the site Macrobrachium rosenbergii ND1 Gene A 571-；
(2) genomic DNA of Macrobrachium rosenbergii to be measured is extracted；
(3) PCR amplification, detection amplification gained genetic fragment are carried out with genomic DNA of the primer pair of step (1) to Macrobrachium rosenbergii
SNP site genotype；
(4) early stage breeding is carried out to Macrobrachium rosenbergii body ruler and growth traits based on the genotype of SNP site.
5. according to the method described in claim 4, it is characterized in that, the sequence of the primer pair of the PCR amplification such as SEQ ID № 1
Shown in 2.
6. according to the method described in claim 4, it is characterized in that, the amplification instrument that uses of the PCR amplification is BIO-RAD
T100PCR instrument.
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109797226A (en) * | 2019-02-26 | 2019-05-24 | 中国水产科学研究院珠江水产研究所 | A kind of Macrobrachium rosenbergii classification method based on EST-SSR label |
| CN110016510A (en) * | 2019-04-22 | 2019-07-16 | 宁波大学 | A kind of molecular labeling for Macrobrachium rosenbergii hereditary and selection |
| CN110029174A (en) * | 2019-04-22 | 2019-07-19 | 浙江省淡水水产研究所 | A kind of SSR marker related to Macrobrachium rosenbergii weight |
| CN111118130A (en) * | 2020-01-15 | 2020-05-08 | 深圳市泽龙生物技术有限公司 | Method for rapidly identifying sex of macrobrachium rosenbergii |
| CN112375827A (en) * | 2020-03-24 | 2021-02-19 | 扬州大学 | SNP marker related to growth of macrobrachium rosenbergii as well as typing method and application thereof |
| CN114395635A (en) * | 2022-03-11 | 2022-04-26 | 广西壮族自治区水产科学研究院 | SNP molecular marker related to growth traits of macrobrachium rosenbergii and application thereof |
| CN114410801A (en) * | 2022-01-26 | 2022-04-29 | 广西壮族自治区药用植物园 | SNP marker influencing growth traits of macrobrachium rosenbergii and application thereof |
| CN114480675A (en) * | 2022-03-04 | 2022-05-13 | 广西壮族自治区药用植物园 | GP gene SNP marker and application thereof |
-
2018
- 2018-08-10 CN CN201810907760.9A patent/CN108977551A/en active Pending
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| AGARWAL ET AL.: "SNP mining in transcripts and concomitant estimation of genetic variation in Macrobrachium rosenbergii stocks", 《CONSERVATION GENETICS RESOURCES》 * |
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Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109797226A (en) * | 2019-02-26 | 2019-05-24 | 中国水产科学研究院珠江水产研究所 | A kind of Macrobrachium rosenbergii classification method based on EST-SSR label |
| CN110016510A (en) * | 2019-04-22 | 2019-07-16 | 宁波大学 | A kind of molecular labeling for Macrobrachium rosenbergii hereditary and selection |
| CN110029174A (en) * | 2019-04-22 | 2019-07-19 | 浙江省淡水水产研究所 | A kind of SSR marker related to Macrobrachium rosenbergii weight |
| CN110016510B (en) * | 2019-04-22 | 2022-06-07 | 宁波大学 | Molecular marker for genetic breeding of macrobrachium rosenbergii |
| CN110029174B (en) * | 2019-04-22 | 2023-01-10 | 浙江省淡水水产研究所 | SSR (simple sequence repeat) marker related to quality of macrobrachium rosenbergii bodies |
| CN111118130A (en) * | 2020-01-15 | 2020-05-08 | 深圳市泽龙生物技术有限公司 | Method for rapidly identifying sex of macrobrachium rosenbergii |
| CN112375827A (en) * | 2020-03-24 | 2021-02-19 | 扬州大学 | SNP marker related to growth of macrobrachium rosenbergii as well as typing method and application thereof |
| CN112375827B (en) * | 2020-03-24 | 2023-10-27 | 扬州大学 | SNP (single nucleotide polymorphism) marker related to growth of macrobrachium rosenbergii as well as typing method and application thereof |
| CN114410801A (en) * | 2022-01-26 | 2022-04-29 | 广西壮族自治区药用植物园 | SNP marker influencing growth traits of macrobrachium rosenbergii and application thereof |
| CN114480675A (en) * | 2022-03-04 | 2022-05-13 | 广西壮族自治区药用植物园 | GP gene SNP marker and application thereof |
| CN114395635A (en) * | 2022-03-11 | 2022-04-26 | 广西壮族自治区水产科学研究院 | SNP molecular marker related to growth traits of macrobrachium rosenbergii and application thereof |
| CN114395635B (en) * | 2022-03-11 | 2023-07-28 | 广西壮族自治区水产科学研究院 | SNP molecular marker related to growth traits of macrobrachium rosenbergii and application of SNP molecular marker |
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