CN105483259B - SNP site relevant to nest litter size on No. 12 chromosomes of pig - Google Patents

SNP site relevant to nest litter size on No. 12 chromosomes of pig Download PDF

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CN105483259B
CN105483259B CN201610002991.6A CN201610002991A CN105483259B CN 105483259 B CN105483259 B CN 105483259B CN 201610002991 A CN201610002991 A CN 201610002991A CN 105483259 B CN105483259 B CN 105483259B
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pig
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genotype
litter size
snp site
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CN105483259A (en
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张亚平
黄路生
谢海兵
任军
艾华水
徐丹
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Kunming Institute of Zoology of CAS
Jiangxi Agricultural University
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Jiangxi Agricultural University
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Abstract

The present invention relates to SNP sites relevant to pig number born character, and in particular to a SNP site relevant to nest litter size and its primer on No. 12 chromosomes of pig belong to field of biotechnology.The SNP site is the Chr12:11177285 of genome version NCBI Build Sscrofa 10.2;The allele in the site is T and C, has tri- kinds of genotype of C/C, T/C and T/T, expands the primer and extension primer in the site are as follows: Chr12-PCRU:5 '-CAA TGC AGA GAT CCA ACT CC-3 ';Chr12-PCRL:5 '-AAA ATC CAG GCG CAG ATC-3 ';Chr12-SNPU:5 '-CTG ACT GAC TGT TCT TTA TCC TGC CCC ATT AAT TA-3 '.Litter size of pig with T/T genotype is higher than T/C genotype, the number born of sow highest with T/T genotype, and the number born of sow with T/C genotype is minimum.The beneficial effects of the present invention are: full-length genome weight sequencing approach can screen SNP site relevant to character or gene quickly, in bulk, this SNP site of the Chr12:11177285 of genome version NCBI Build Sscrofa 10.2 can improve the litter size of sow as genetic marker for the genetic breeding of pig.

Description

SNP site relevant to nest litter size on No. 12 chromosomes of pig
Technical field:
The present invention relates to SNP sites relevant to pig number born character, and in particular to one and nest on No. 12 chromosomes of pig The relevant SNP site of litter size and its primer belong to field of biotechnology.
Background technique:
The characters of number born of pig is the chief component of pig reproductive trait, improves litter size of pig to the total of raising pig breeding industry Body economic benefit is significant.The Taihu pigs in China are well-known with high yield, and nest litter size is than most of other Chinese native pig breeds And the nest litter size of external pig kind is 4-5 more (" Chinese pig breeds will " Zhang Zhongge chief editor, Shanghai Scientific & Technical Publishers, 1986). Polymorphic site relevant to high litter size in Taihu pigs can be used to improve the litter size of sow as genetic marker.
Full-length genome weight sequencing approach is widely used to the correlative study of each species, it quickly can comprehensively be screened Gene relevant to character, function or mutational site out, compensate for QTL positioning and candidate gene approach is time-consuming and laborious, single The deficiencies of.
At home and abroad there is not yet SNP site open source literature relevant to Litter Size in Pigs is reported in the present invention.
Summary of the invention:
The object of the present invention is to provide a SNP site relevant to nest litter size and its primers on No. 12 chromosomes of pig.
The present invention has selected Erhualian (one kind of Taihu pigs), hides pig, BaMa miniature pig, Laiwu Pigs and the southern regions of the Yunnan Province microtia pig 5 A Chinese native pig breed and wild boar have carried out full-length genome and have resurveyed sequence.The sequence number of individuals of resurveying of 6 pig kinds is respectively 11, and 11 It is a, 9,10,10 and 10.Weight sequencing data is compared with reference genome (NCBI Build Sscrofa 10.2) It is right, the extraction in the site SNPs is carried out using SAMTools software.Inventor compares Erhualian and other 5 pig kinds, 12 A SNP site (Chr12:11177285 of genome version NCBI Build Sscrofa 10.2) is found on number chromosome It is related to the litter size of pig.The allele in the site is T and C, there is tri- kinds of genotype of C/C, T/C and T/T.
After screening the site, inventor hybridizes resource population F in white Duroc × Erhualian2It is right in godmother's pig individual It carries out verifying and correlation analysis, as a result, it has been found that there is significant correlation in the site with litter size of pig.
The beneficial effects of the present invention are: full-length genome weight sequencing approach can screen related to character quickly, in bulk SNP site or gene, this SNP site of the Chr12:11177285 of genome version NCBI Build Sscrofa 10.2 The litter size of sow can be improved for the genetic breeding of pig as genetic marker.
Detailed description of the invention:
Fig. 1 is white Duroc × Erhualian F23 kinds of the site Chr12:11177285 genotype in godmother's pig resource population Litter size compare (when two kinds of genotype litter sizes compare in figure, * indicate 0.01≤P≤0.05;* indicates P < 0.01).
Specific embodiment:
(1) the population distribution feature of SNP site
The present invention selects Erhualian (one kind of Taihu pigs), hides pig, BaMa miniature pig, Laiwu Pigs and the southern regions of the Yunnan Province microtia pig 5 Chinese native pig breed and wild boar have carried out full-length genome and have resurveyed sequence.The sequence number of individuals of resurveying of 6 pig kinds is respectively 11, and 11 It is a, 9,10,10 and 10.Weight sequencing data is compared with reference genome (NCBI Build Sscrofa 10.2) It is right, the extraction in the site SNPs is carried out using SAMTools software.Inventor compares Erhualian and other 5 pig kinds, 12 A SNP site (Chr12:11177285 of genome version NCBI Build Sscrofa 10.2) is found on number chromosome It is related to the litter size of pig.
(2) identification of SNP site
In design of primers website design SNAPSHOT primer, including a pair of of PCR amplification primer (Chr12-PCRU:5 '-CAA TGC AGA GAT CCA ACT CC-3';Chr12-PCRL:5 '-AAA ATC CAG GCG CAG ATC-3 ') and extension primer (Chr12-SNPU:5 '-CTG ACT GAC TGT TCT TTA TCC TGC CCC ATT AAT TA-3 ').The site and its Totally 24, its 11 site (12 pairs) primer respectively takes 1 μ l to be mixed into new multiple PCR primer pond.12 weight PCR reactions are carried out first, Reaction system agents useful for same are as follows: multiple PCR primer pond (6.25 μM of each) 8 μ l, dNTP (10mM each) 8 μ l, 10 × PCR Buffer II 116μl、MgCl2(25mM Stock) 234 μ l, Fast Start Taq (5U/ μ l) 24 μ l and ddH2460 μ l of O, The above 8.5 μ l of reagent mixed liquor and 1.5 μ l DNA (50ng/ μ l) are mixed into 10 μ l systems and carry out 12 heavy pcr amplification reactions.Expand Increase reaction condition are as follows: 94 DEG C of 4min;94 DEG C of 30s, 55 DEG C of 30s, 72 DEG C of 1min, totally 40 recycle.It is anti-that PCR is carried out in next step Should purify, required reagent are as follows: Exo I (10U/ μ l) 60 μ l, SAP (1U/ μ l) 130 μ l, 10 × SAP Buffer, 35 μ l and ddH2125 μ l of O is carried out after the above-mentioned purifying mixed liquor centrifugation of 3.5 μ l is added in the PCR product of each sample by following procedure Reaction: 37 DEG C of 40min, 96 DEG C of 10min.Then single base extension, required reagent are as follows: SNAPSHOT are carried out (6.25 μM of each, 12 extension primers respectively take 1 μ l for 100 μ l of Multiplex ready reaction Mix, extension primer pond Mixing) 8 μ l, 5 × Sequencing Buffer 200 μ l and ddH2300 μ l of O, by the pure of the above 6 μ l of reagent mixed liquor and 4 μ l Change product and is mixed into 10 μ l systems progress extension.Extension condition are as follows: 96 DEG C of 10s, 50 DEG C of 5s, 60 DEG C of 30s, altogether 25 circulations.Then the purifying of extension product, required reagent are as follows: SAP (1U/ μ l) 120 μ l, 10 × SAP Buffer are carried out 70 μ l and ddH2140 μ l of O, be added in the extension product of each sample after above-mentioned 3.3 μ l purifying mixed liquor centrifugation by with Lower program is reacted: 37 DEG C of 40min, 75 DEG C of 20min, 4 DEG C save backup.Each sample takes 5-4 μ l above-mentioned after purification High-purity formamide (Hi-Di Formamide) of SNAPSHOT reaction product and 5-6 μ l are mixed into loading after the centrifugation of 10 μ l systems Genotyping is carried out in ABI 3730XL sequenator, analyzes genotyping result using GeneMarker software.
(note: the reaction reagent mixed liquor dosage of above 4 steps is amount of reagent needed for 100 samples, is prolonged from single base It stretches reaction to start, needs to be carried out in the dark.)
(3) white Duroc × Erhualian reproductive performance hybridization resource population building
Subsequent confirmatory experiment used resource group individual sample and its trait data are by Agricultural University Of Jiangxi's animal organism skill Art National Key Laboratory cultivation base provides.
In December, 1998, two will bought from the 3 Erhualian conservation fields in Jiangsu Province on Agricultural University Of Jiangxi's scientific research pig farm Paint face sow carries out the intersection breeding of blood relationship between field.In January, 2001 according to parent's Farrowing Traits, from 3 boars and 11 sows Pure breeding offspring in selected 17 Erhualian sows as the maternal for generations of sources group.2 that Sygen PIC company is given For generations male parent of the high-quality white Duroc boars as Resource family.This 2 white Durocs and 17 Erhualians are miscellaneous Hand over the F generated1Breed for individual, avoid full, and every boar usually with same head insemination of sows, to obtain The F of large sample2Family half sibs.In January, 2003, March and June, project team is respectively by the 1st batch and the 2nd crowd of F2Sow is sent to Jiangxi Save Yichun City herding seed multiplication farm (59), Jiangxi Province state-run Red Star kind pig farm (52) and Jiangxi Shangyou County quaternionic breeding pig farm (118) are used for the measurement of sow reproductive trait.
(4) SNP site is in hybridization resource population F2The Genotyping of godmother's pig groups
According to method described in above-mentioned steps (2), hybridize resource population F with 192 white Duroc × Erhualians2Godmother Pig individual DNA is the genotype of the template detection SNP site.192 F2For resource population individual in there are 168 individuals successfully to divide The number of individuals of type, 3 kinds of genotype C/C, T/C and T/T is 10,65 and 93 respectively.
(5) regulating effect of the SNP site to characters of number born
In F2For in resource population individual, the average litter size with C/C genotype individuals is 11.6288, and standard deviation is 1.0845;Average litter size with T/C genotype individuals is 10.2746, standard deviation 0.8118;With T/T genotype The average litter size of body is 11.649, standard deviation 0.7845.
The present invention analyzes influence of the SNP site to pig total yield coefficient, number born alive using general linear model (GLM). All statistical analysis is carried out using SAS software.Model is as follows:
Yijklm=u+Ai+Gj+Bk+Pl+eijklm
Wherein YijklmFor pig total yield coefficient or number born alive, u is group's mean value, AiFor the additive effect of i-th of individual, Gj For the fixed effect of j-th of SNP site genotype, BkFor batch effect (k=1,2,3,4), PlFor stochastic effects (l=1,2, 3)。
Analysis is as a result, it has been found that this SNP site of Chr12:11177285 has significant correlation with litter size.With T/T gene The F of type2The litter size of godmother pig is averaged more 1.3744 (P=0.005), as can be seen from Figure 1, band than the sow with T/C genotype There is the number born of sow highest of T/T genotype, the number born of sow with T/C genotype is minimum.
Find out from SNP site and litter size correlation analysis, this SNP site of Chr12:11177285 can be used as molecule Apply the tag to the litter size of molecular marker assisted selection (MAS) Lai Tigao sow.

Claims (1)

1. primer the answering in detection litter size of pig of SNP site relevant to nest litter size on a kind of detection No. 12 chromosomes of pig It include PCR amplification primer and extension primer with, it is characterised in that: the primer, the wherein nucleotide sequence of PCR amplification primer It is as follows: Chr12-PCRU:5 '-CAATGCAGAGATCCAACTCC-3 ';Chr12-PCRL:5 '- AAAATCCAGGCGCAGATC-3';The nucleotide sequence of extension primer is as follows: (Chr12-SNPU:5 '- CTGACTGACTGT TCTTTATCCTGCCCCATTAATTA-3 ', the pig are that white Duroc × Erhualian hybridizes resource Group F2 godmother pig, the SNP site are the Chr12:11177285 of genome version NCBI Sscrofal10.2, the site Allele is T and C, there is tri- kinds of genotype of C/C, T/C and T/T, the litter size of pig with C/C genotype be higher than with T/C and The pig of T/T genotype, wherein allele C is to improve the beneficial allele of litter size of pig.
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Publication number Priority date Publication date Assignee Title
CN107287329B (en) * 2017-07-28 2021-02-09 深圳华大生命科学研究院 SNP locus combination and method for predicting genetic performance of litter size alive piglets of pigs to be tested
CN107365842B (en) * 2017-07-28 2021-01-26 深圳华大生命科学研究院 SNP locus combination and method for predicting genetic performance of total litter size of pigs to be tested
CN109486956B (en) * 2017-09-11 2021-11-02 中国农业科学院北京畜牧兽医研究所 Multi-group integrated precise breeding method for pigs
CN108570505B (en) * 2017-09-11 2021-03-26 中国农业科学院北京畜牧兽医研究所 Multi-group integrated precise breeding method for pigs
CN111705145B (en) * 2020-07-30 2021-07-13 江西农业大学 SNP marker influencing guanine content in pig individual

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