3.9 Article

Genetic variation in the first intron and exon of the myostatin gene in several Indonesian cattle populations

期刊

VETERINARY WORLD
卷 14, 期 5, 页码 1197-1201

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VETERINARY WORLD
DOI: 10.14202/vetworld.2021.1197-1201

关键词

beef cattle; double muscling; myostatin gene; polymorphisms; single-nucleotide polymorphism

资金

  1. Ministry of Agriculture of the Republic of Indonesia through the Agency of Agricultural Research and Development [SP DIPA-018.09.2.648720/2020]

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This study aimed to detect the genetic variation of the MSTN gene in cattle populations raised in Indonesia. Several nucleotide substitutions and insertions were found, with two loci showing polymorphism in all populations. Different genotypes had varying frequencies among the populations.
Background and Aim: Myostatin (MSTN), a member of the transforming growth factor-beta family, is a negative regulator of muscle mass. This study aimed to detect the genetic variation of the 1160 bp fragment of exon 1 and part of intron 1 of the MSTN gene in several cattle populations raised in Indonesia. Materials and Methods: Polymerase chain reaction products of the MSTN gene amplified from 92 animals representing 10 cattle populations (Peranakan Ongole [PO], Belgian Blue x PO cross, Rambon, PO x Bali cross, Jabres, Galekan, Sragen, Donggala, Madura, and Bali) were sequenced, compared, and aligned with bovine MSTN of Bos taurus (GenBank Ace. No. AF320998.1) and Bos indicus (GenBank Ace. No. AY794986.1). Results: Four nucleotide substitutions (nt 1045 and 1066 in intron 1; nt 262 and 418 in exon 1) and two indels (nt 807 and 869 in intron 1) were synonymous mutations. Among these substitutions, only the nt 262G>C and nt 418A>G loci were polymorphic in all populations, except Bali cattle. The frequencies of the nt 262C (0.82) and nt 418A (0.65) alleles were highest. For the nt 262G>C locus, the CC genotype had the highest frequency (0.66) followed by GC (0.30) and CC (0.03). For the nt 418A>G locus, the AG genotype had the highest frequency (0.52) followed by AA (0.39) and GG (0.09). Conclusion: The results, showing genetic variations in cxon 1 and intron 1 of the MSTN gene, might be helpful for future association studies.

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