CN101067151A - Primer, segment and method for identifying sex of air potato - Google Patents
Primer, segment and method for identifying sex of air potato Download PDFInfo
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- CN101067151A CN101067151A CNA2007100228291A CN200710022829A CN101067151A CN 101067151 A CN101067151 A CN 101067151A CN A2007100228291 A CNA2007100228291 A CN A2007100228291A CN 200710022829 A CN200710022829 A CN 200710022829A CN 101067151 A CN101067151 A CN 101067151A
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Abstract
The present invention belongs to the field of molecular marker technology, and discloses primers, segment and method for identifying the sex of air potato plant. The segment has the nucleotide sequence as shown in SEQ ID No. 1; and the primers have the nucleotide sequences as shown in SEQ ID No. 2 and SEQ ID No. 3. Using the primers in PCR reaction can obtain amplified segment of 677 bp length from male air potato plant and no any amplified product can be obtained from female air potato plant. Therefore, the primers are male air potato plant specific and may be used in identifying the sex of air potato plant.
Description
Technical field:
The invention belongs to the molecular marking technique field, is one group of primer, fragment and method of differentiating sex of air potato.
Background technology:
Air potato Dioscorea bulbifera L. is a Dioscoreaceae Dioscoreaceae Wild yam Dioscorea L. plant, and cosmopolitan intersperses among ground such as Africa, America and Asia.The air potato flower unisexuality, dioecy, and the sex performance is stable.Air potato stem tuber and Bulbilus dioscoreae (bulbil) rich in starch and sugar, the extensively cultivation and edible on Africa, South East Asia and Polynesia and other places.The air potato stem tuber is a conventional Chinese medicine in China, has another name called Rhizoma Dioscoreae Bulbiferae, and it is cool in nature, and bitter has that dissipating bind is become thin, clearing heat and detoxicating a, cooling blood for hemostasis, anticancer effect.With air potato generic Rhizome of Peltate Yam Dioscorea zingiberensis C.H.Wright, contain diosgenin in its rhizome, it is the important medicine source plant resource of steroid hormone class medicine, and there are some researches show, diosgenin content in its staminiferous plant rhizome is higher than female plant, and therefore growing upward, early screening has important economic value to the male plant of Rhizome of Peltate Yam.But under cultivation condition, the sex performance more complicated of Rhizome of Peltate Yam, there is not the generic air potato stable, therefore find a kind of dna marker to differentiate that the early stage air potato plant of growth has important use and is worth from molecular level, the early stage male and female of Rhizome of Peltate Yam plant are differentiated to have important practice significance.
Since nineteen ninety Williams and Welsh foundation RAPD (Random Amplified polymorphie DNA) technology, this technology successfully is used for the study on sex-related difference of plant.SCAR (sequence characterized amplified region) molecule marker, be to carry out pcr amplification according to the The sequencing results of RAPD molecule marker with the special primer of 20-28 base to obtain, can repeat the amplification of high specific to the genome localized area.The RAPD-SCAR labeling technique is succeedd in the sex research of a lot of plants at present, as RAPD-SCAR male mark, papaya (Carica papaya L.) the RAPD-SCAR male marker of hemp (Cannabis sativa L.) with Y linkage.
Still do not have the report that relevant molecule marker is differentiated the sex of air potato method at present both at home and abroad, the present invention has filled up the blank in this field.
Summary of the invention:
The object of the invention provides one group of primer and the section of DNA fragment of differentiating sex of air potato;
Another object of the present invention provides a kind of method of differentiating sex of air potato.
The present invention uses the RAPD method to amplify a male specific band in male air potato genome, having obtained a segment length by clone and order-checking is the dna sequence dna (SEQ ID NO:1) of 681bp, and according to this sequences Design one group of primer of differentiating sex of air potato, its sequence is shown in SEQ ID NO:2 and SEQ ID NO:3, can increase in the air potato genome to primer according to this obtains a male specific sequence, and its length is 677bp.
The invention provides a kind of method of differentiating sex of air potato, it is characterized in that method is the sex that per sample PCR reaction product agarose gel electrophoresis result identifies sample.Auele Specific Primer is SEQ ID NO:2 and SEQ ID NO:3 in this method.The band that length is 677bp appears in PCR product electrophoresis result in this method, and this sample is a staminiferous plant, is female plant and the sample of band does not appear in same area.
The PCR reaction system is 20 μ l, and reaction solution consists of 10 * PCRbuffer, the dNTPs of 2.5mmol/L, the MgCl of 25mmol/L
2, the Taq archaeal dna polymerase of lu, 0.4 μ mol/L random primer, 20-50ng template DNA.On PE-9600 PCR instrument, carry out pcr amplification: 94 ℃ of pre-sex change 3min by following cycling program; 94 ℃ of sex change 45s, 38 ℃ of annealing 30s, 72 ℃ are extended 90s, 35 circulations; Last 72 ℃ are extended 5min, 4 ℃ of preservations.
The present invention has tested 100 RAPD random primers altogether, available from the biological company limited of Shanghai English fine horse, in male air potato genome, amplify a male specific band of 681bp (its dna sequence dna is SEQ ID NO:1), contain a plurality of terminators, belong to non-coding sequence, this sequence is carried out sequence alignment on Genebank, do not find homologous sequence with it.According to this specific band sequencing result, design a pair of Auele Specific Primer SEQ ID NO:2 and SEQ ID NO:3.
Design a pair of SCAR special primer according to complete sequence:
SEQ?ID?NO：2 5′-GGCTTCTGTCACTACATGGG-3′
SEQ?ID?NO：3 5′-GGCTTCTGTCCAGTGCATCT-3′
This validity of the individual check of 35 air potatoes by known sex to primer, SCAR reaction shows in all 13 air potato staminiferous plant DNA of individual electrophoresis result and the 677bp band all occurred, and this band (Fig. 1,2) does not appear in corresponding site in 22 air potato female individuals.
In sum, the invention provides a segment length is the specific dna sequence dna of air potato male and female of 681bp, can be used for the male and female sex identification of air potato.Assay has proved that primer and PCR method among the present invention can accurately identify the sex of air potato male and female.
Description of drawings:
Fig. 1 RAPD-SCAR mark individual plant detected result 1 wherein has a specific band on the electrophoretic band of 13 staminiferous plants (1-13).M:100bp Ladder dna molecular amount mark.Arrow 1 is depicted as the male relevant SCAR mark of air potato, and arrow 2 is depicted as primer dimer.
There is not band on the 677bp position of Fig. 2 RAPD-SCAR mark individual plant 2,22 female plants of detected result (14-35).M:100bp Ladder dna molecular amount mark.Arrow 2 is depicted as primer dimer.
Embodiment:
1. the acquisition of plant genome DNA and RAPD-SCAR mark
Adopt the CTAB method from the air potato spire, to extract DNA, after the DNA purifying that the DNA of extraction produces with the rich Bioexperiment Materials Research Laboratories of Beijing Lay reclaims the test kit purifying, be dissolved in the sterilization distilled water ,-20 ℃ of storages, standby.Get the high eyebrow in the Sichuan female, that staminiferous plant is complete, Tianlin County, Guangxi, 3 the wild air potatoes of population in Mengzi, Yunnan are male and female each 1 strain, with individual plant DNA sample balanced mix, build up male respectively or female dna pond (DNA pools), so that female, the male dna sample with identical genetic background to be provided.
The random primer screening adopts the mixing fractional analysis method (BSA) of Michelmore to carry out.Amplification reaction system is 20 μ l, and reaction solution consists of 10 * PCRbuffer, the dNTPs of 2.5mmol/L, the MgCl of 25mmol/L
2, the Taq archaeal dna polymerase of lu, 0.4 μ mol/L random primer, 20-50ng template DNA.On PE-9600 PCR instrument, carry out pcr amplification: 94 ℃ of pre-sex change 3min by following cycling program; 94 ℃ of sex change 45s, 38 ℃ of annealing 30s, 72 ℃ are extended 90s, 35 circulations; Last 72 ℃ are extended 5min.1.2% agarose gel electrophoresis (80V 1h) detects the pcr amplification result, ethidium bromide (EB) dyeing, and the ultraviolet gel imaging system is taken pictures, and 100bp DNA Ladder makes molecular weight marker.
The PCR product is purified, behind the Pignus pignoris grain, select 1 cloning and sequencing, and its dna sequence dna is SEQ ID NO:1.According to the dna sequence analysis result, design the Auele Specific Primer of a pair of 20 bases.This is SEQ ID NO:2 and SEQ ID NO:3 to primer among the present invention.
2.PAPD-SCAR the confirmatory experiment of molecule marker
With SEQ ID NO:2 and SEQ ID NO:3 this to primer, with 12 population totally 35 individual plant DNA be that template is carried out pcr amplification.Amplification reaction system is 20 μ l, and reaction solution consists of 10 * PCRbuffer, the dNTPs of 2.5mmol/L, the MgCl of 25mmol/L
2, the Taq archaeal dna polymerase of lu, each 0.3 μ mol/L of upstream and downstream primer, 50ng template DNA.On PE-9600 PCR instrument, carry out pcr amplification: 94 ℃ of pre-sex change 3min by following cycling program; 94 ℃ of sex change 45s, 62 ℃ of annealing 30s, 72 ℃ are extended 90s, 35 circulations; Last 72 ℃ are extended 5min.1.2% agarose gel electrophoresis (80V 1h) detects the pcr amplification result, ethidium bromide (EB) dyeing, and the ultraviolet gel imaging system is taken pictures, and 100bp DNA Ladder makes molecular weight marker.
Result such as Fig. 1 shown in 2, have a specific band on the electrophoretic band 677bp position of 13 staminiferous plants (1-13) among Fig. 1, and do not have band on the 677bp position of 22 female plants (14-35) in Fig. 2.This primer and method that shows that the present invention designs can be used in air potato male and female sex identification.
Sequence table
＜110〉Institute of Botany
＜120〉primer, fragment and the method for discriminating sex of air potato
<160>3
<210>1
<211>681
<212>DNA
＜213〉derive from air potato (Dioscorea bulbifera L.)
<400>1
ggcttctgtc?actacatggg?atgaggtggt?agaggctttt?ctcgcatgat?acttcttgtt?60
tggaaaacca?gcaaagcata?acaatgaaat?cttgtcctat?gtacaaaata?agcgggagtc?120
cttatttgag?acttgggaga?aatttaagga?tctcttgtgg?cggtgccccc?aacatggatt?180
tctccattgg?atggtagctc?acacattttc?ttatgggctc?aatttgagca?ctaggtaact?240
cttagatgtc?attgcaagag?gtaatttggg?taacaagacc?tagaagatgc?tagacagctc?300
atagagtgtc?acgcctggac?ccgccgacat?ggcacacaac?ataccgccat?gacaacccaa?360
cgcaaagtga?acaccgccaa?gaccatgagt?tatcgtaagg?atagcatatt?tcctgtttac?420
aaacactggt?ataactggga?aagataacaa?ctcatgatga?tatattctca?agaaaatata?480
tatacgcata?aggtaataca?tgtcctcaat?acgagtttta?atacaacagt?ttgacattaa?540
caagcttaga?atttccaaga?tagaagaaca?aaatgcaaga?aatccaaatg?aatacagtaa?600
tggatcccat?gactacatgt?cacaacagat?aagaagacct?acacaatgca?atacaagaga?660
tgcactggac?agaagccaat?c 681
<210>2
<211>20
<212>DNA
＜213〉artificial primer
<400>2
ggcttctgtc?actacatggg?20
<210>3
<211>20
<212>DNA
＜213〉artificial primer
<400>3
ggcttctgtc?cagtgcatct?20
Claims (4)
1. air potato medicinal material dna molecular is identified the specificity segment of sex, and its sequence is shown in the SEQ ID NO:1.
2. air potato medicinal material dna molecular is identified one group of primer of sex, and this group primer is by sequences Design synthetic shown in the SEQ ID NO:1, and its sequence is shown in SEQ ID NO:2 and the SEQ ID NO:3.
3. air potato medicinal material dna molecular is identified the method for sex, it is characterized in that this method is to utilize sequence to carry out the PCR reaction for the primer shown in SEQ ID NO:2 and the SEQ ID NO:3 to identifying sample, agarose gel electrophoresis result by the PCR reaction product identifies sample then, the sample that occurs one section 677bp left and right sides band among the electrophoretic result of PCR product is a staminiferous plant, and same area the sample of band not occur be female plant.
4. want 3 described methods according to right, it is characterized in that this reaction system is 20 μ l, reaction solution consists of: reaction solution consists of 10 * PCRbuffer, the dNTPs of 2.5mmol/L, the MgCl of 25mmol/L
2, the Taq archaeal dna polymerase of 1u, each 0.3 μ mol/L of upstream and downstream primer, 50ng template DNA; On the PCR instrument, carry out pcr amplification: 94 ℃ of pre-sex change 3min by following cycling program; 94 ℃ of sex change 45s, 62 ℃ of annealing 30s, 72 ℃ are extended 90s, 35 circulations; Last 72 ℃ are extended 5min; 1.2% agarose gel electrophoresis (80V 1h) detects the pcr amplification result, ethidium bromide (EB) dyeing, and the ultraviolet gel imaging system is taken pictures, and 100bp DNA ladder makes molecular weight marker; The sample that occurs one section 677bp band in this method in the PCR product electrophoresis result is male, and same area the sample of band not occur be female plant.
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| CNB2007100228291A CN100547082C (en) | 2007-05-23 | 2007-05-23 | Differentiate primer, fragment and the method for sex of air potato |
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| CNB2007100228291A CN100547082C (en) | 2007-05-23 | 2007-05-23 | Differentiate primer, fragment and the method for sex of air potato |
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| CN101067151A true CN101067151A (en) | 2007-11-07 |
| CN100547082C CN100547082C (en) | 2009-10-07 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102433389A (en) * | 2012-01-06 | 2012-05-02 | 中国林业科学研究院热带林业研究所 | DNA (deoxyribonucleic acid) fragment, primers and method for identifying gender of salak |
| CN103255207A (en) * | 2013-01-15 | 2013-08-21 | 内蒙古农牧业科学院 | Molecular detection method for brassica campestris seeds carrying brassica campestris leptosphaeria maculans pathogenic bacterial |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6037128A (en) * | 1997-03-31 | 2000-03-14 | Council Of Scientific & Industrial Research | Process for the preparation of semisynthetic amplicon useful for sex determination of the papaya plant |
| US6180345B1 (en) * | 1998-03-31 | 2001-01-30 | Counsel Of Scientific & Industrial Research | Process for simultaneous preparation of sex specific and gender-neutral semisynthetic amplicons useful for sex determination |
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2007
- 2007-05-23 CN CNB2007100228291A patent/CN100547082C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102433389A (en) * | 2012-01-06 | 2012-05-02 | 中国林业科学研究院热带林业研究所 | DNA (deoxyribonucleic acid) fragment, primers and method for identifying gender of salak |
| CN102433389B (en) * | 2012-01-06 | 2013-06-19 | 中国林业科学研究院热带林业研究所 | DNA (deoxyribonucleic acid) fragment, primers and method for identifying gender of salak |
| CN103255207A (en) * | 2013-01-15 | 2013-08-21 | 内蒙古农牧业科学院 | Molecular detection method for brassica campestris seeds carrying brassica campestris leptosphaeria maculans pathogenic bacterial |
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| CN100547082C (en) | 2009-10-07 |
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Granted publication date: 20091007 Termination date: 20100523 |