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Nucleotide sequence and variations of the bovine myocyte enhancer factor 2C (MEF2C) gene promoter in Bos Taurus cattle

机译:牛金牛座牛肌细胞增强因子2C(MEF2C)基因启动子的核苷酸序列和变异

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摘要

Myocyte Enhancer Factor 2 (MEF2) proteins are a small family of transcription factors that play pivotal role in morphogenesis and myogenesis of skeletal, cardiac, and smooth muscle cells. In vertebrates, there are four MEF2 genes, referred to as MEF2A, -B, -C, and -D, that are located on different chromosomes. After birth MEF2A, MEF2B, MEF2D transcriptions are expressed ubiquitously, whereas MEF2C transcripts are restricted to skeletal muscle, brain, and spleen. In this study, on the basis of the sequences of the bovine chromosome 7 genomic contig, available in the GenBank database, sets of PCR primers were designed and to amplify the bovine MEF2C gene promoter region, exon 1 (5′UTR) and part sequence of the intron 1. Seven overlapping fragments of the bovine MEF2C gene were amplified and then sequenced. Altogether, these fragments were composed in the 3,120-bp sequence which was deposited in the GenBank database under accession no. . The sequence fragment included the putative site of the promoter region and transcription start of the exon 1. The sequence analysis of these fragments in individual animals representing different Bos taurus breeds revealed four variations in promoter region: g.-1606C>T, g.-1336_-1335DelG, g.-818C>T, g.-613_-612DelA and four SNPs within intron 1: g.2711A>G, g. 2913A>G, g.2962G>T and g.3014A>G. No polymorphism was found within sequence of the exon 1 (5′UTR). These polymorphisms were identified for first time using these sequences and were confirmed by RFLP or MSSCP methods.
机译:肌细胞增强因子2(MEF2)蛋白是一小类转录因子,在骨骼肌,心脏和平滑肌细胞的形态发生和成肌中起关键作用。在脊椎动物中,有四个位于不同染色体上的MEF2基因,分别称为MEF2A,-B,-C和-D。出生后,MEF2A,MEF2B,MEF2D转录无处不在,而MEF2C转录本仅限于骨骼肌,大脑和脾脏。在这项研究中,根据GenBank数据库中的牛7号染色体基因组重叠群的序列,设计了PCR引物对,并扩增了牛MEF2C基因启动子区域,外显子1(5'UTR)和部分序列内含子1.扩增牛MEF2C基因的七个重叠片段,然后测序。这些片段总共以3120 bp的序列组成,并在GenBank数据库中以登录号No.存放。 。序列片段包括启动子区域的假定位点和外显子1的转录起点。在代表不同金牛座牛的各个动物中对这些片段进行的序列分析显示,启动子区域有四个变异: g。- 1606C T ,g .- 1336 _ - 1335DelG ,g .- 818C > T ,g .- 613 _ - 612DelA 和内含子1中的四个SNP:g。 2711A G ,g。 2913A G ,g。 2962G T 和g。 3014A G。在第1外显子( 5'UTR )的序列中未发现多态性。使用这些序列首次鉴定出这些多态性,并通过 RFLP MSSCP 方法进行了确认。

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