2011
DOI: 10.17221/4415-cjas
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Polymorphism identification in the goat MSTN gene and association analysis with growth traits

Abstract: ABSTRACT:The myostatin (MSTN) gene was studied as a candidate genetic marker for growth traits. We investigated polymorphisms of the MSTN gene in 664 individuals from four goat populations and applied PCR-SSCP and DNA sequencing analysis to reveal two single nucleotide polymorphisms (DQ167575: g.368A>C (p.Lys49Thr) and g.4911C>T. At g.368A>C locus, the frequencies of g.368A allele were 0.75-0.81, and the frequencies of g.368C allele were 0.19-0.25. At g.4911C>T locus, the frequencies of g.4911C allele were 0.7… Show more

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Cited by 11 publications
(6 citation statements)
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“…The SSCP analysis of PCR products of primer pair 2 refers to An et al (2011) [17]. In addition, PCR products (5μl) of primer pair 2 were mixed with 1 μl 10 × buffer, 3 U Eco81Ⅰ(TaKaRa, Dalian, China) and 3.5 μl sterilized ddH2O, and then incubated for 1.5 h at 37°C.…”
Section: Snp Genotyping and Sequencingmentioning
confidence: 99%
“…The SSCP analysis of PCR products of primer pair 2 refers to An et al (2011) [17]. In addition, PCR products (5μl) of primer pair 2 were mixed with 1 μl 10 × buffer, 3 U Eco81Ⅰ(TaKaRa, Dalian, China) and 3.5 μl sterilized ddH2O, and then incubated for 1.5 h at 37°C.…”
Section: Snp Genotyping and Sequencingmentioning
confidence: 99%
“…The present study in Marwari goat revealed low genetic diversity in exon 3 of MSTN gene which is in agreement with the similar study conducted in Saanen and Boer × Guanzhong goats by An et al . [ 27 ], who also observed one homozygote and a heterozygote genotypic pattern revealed by SSCP in exon 3 of caprine MSTN gene. However, a similar type of study in Sanjabi and Zel sheep by Soufy et al .…”
Section: Resultsmentioning
confidence: 97%
“…Each 25 µL reaction contained 50 ng of sample DNA, 0.4 µM of each primer, 1X PCR buffer (10 mMTris-HCl, pH 8.0, 50 mM KCl), 2.0 mM MgCl2, 0.2 mM of each dNTP and 1 U of Taq DNA polymerase (Invitrogen). Amplification reactions were carried out in a thermocycler (Applied BioSystem), with 5 3 F-TCTTTAATAATGACTCCCTGCG R-GAACACCCACAGCGATCTACT [12] min denaturation at 95˚C, 35 cycles of 94˚C for 1 min, 59˚C for 1 min and a 72˚C extension for 1 min, and a final extension at 72˚C for 4 min. Sequencing was performed at Macrogen Inc. Korea, with an automated sequencer (Applied Biosystems) (Figure 1).…”
Section: Methodsmentioning
confidence: 99%