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首页> 外文期刊>BMC Genetics >Myostatin-2 gene structure and polymorphism of the promoter and first intron in the marine fish Sparus aurata: evidence for DNA duplications and/or translocations
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Myostatin-2 gene structure and polymorphism of the promoter and first intron in the marine fish Sparus aurata: evidence for DNA duplications and/or translocations

机译:Myostatin-2基因结构和启动子和第一内含子在海鱼Sparus aurata中的多态性:DNA复制和/或易位的证据

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Background Myostatin (MSTN) is a member of the transforming growth factor-? superfamily that functions as a negative regulator of skeletal muscle development and growth in mammals. Fish express at least two genes for MSTN: MSTN-1 and MSTN-2. To date, MSTN-2 promoters have been cloned only from salmonids and zebrafish. Results Here we described the cloning and sequence analysis of MSTN-2 gene and its 5' flanking region in the marine fish Sparus aurata (saMSTN-2). We demonstrate the existence of three alleles of the promoter and three alleles of the first intron. Sequence comparison of the promoter region in the three alleles revealed that although the sequences of the first 1050 bp upstream of the translation start site are almost identical in the three alleles, a substantial sequence divergence is seen further upstream. Careful sequence analysis of the region upstream of the first 1050 bp in the three alleles identified several elements that appear to be repeated in some or all sequences, at different positions. This suggests that the promoter region of saMSTN-2 has been subjected to various chromosomal rearrangements during the course of evolution, reflecting either insertion or deletion events. Screening of several genomic DNA collections indicated differences in allele frequency, with allele 'b' being the most abundant, followed by allele 'c', whereas allele 'a' is relatively rare. Sequence analysis of saMSTN-2 gene also revealed polymorphism in the first intron, identifying three alleles. The length difference in alleles '1R' and '2R' of the first intron is due to the presence of one or two copies of a repeated block of approximately 150 bp, located at the 5' end of the first intron. The third allele, '4R', has an additional insertion of 323 bp located 116 bp upstream of the 3' end of the first intron. Analysis of several DNA collections showed that the '2R' allele is the most common, followed by the '4R' allele, whereas the '1R' allele is relatively rare. Progeny analysis of a full-sib family showed a Mendelian mode of inheritance of the two genetic loci. No clear association was found between the two genetic markers and growth rate. Conclusion These results show for the first time a substantial degree of polymorphism in both the promoter and first intron of MSTN-2 gene in a perciform fish species which points to chromosomal rearrangements that took place during evolution.
机译:背景Myostatin(MSTN)是转化生长因子-?作为哺乳动物骨骼肌发育负增长调节剂的超家族。鱼表达至少两个MSTN基因:MSTN-1和MSTN-2。迄今为止,仅从鲑鱼和斑马鱼中克隆了MSTN-2启动子。结果在这里我们描述了海洋鱼类Sparus aurata(saMSTN-2)中MSTN-2基因及其5'侧翼区域的克隆和序列分析。我们证明了启动子的三个等位基因和第一个内含子的三个等位基因的存在。三个等位基因中启动子区域的序列比较显示,尽管在三个等位基因中翻译起始位点上游前1050 bp的序列几乎相同,但在上游还存在较大的序列差异。仔细分析三个等位基因中第一个1050 bp上游区域的序列,确定了一些元素,这些元素似乎在某些或所有序列中的不同位置重复出现。这表明saMSTN-2的启动子区域在进化过程中经历了各种染色体重排,反映了插入或缺失事件。对几个基因组DNA集合的筛选显示等位基因频率上的差异,等位基因“ b”最丰富,其次是等位基因“ c”,而等位基因“ a”相对较少。 saMSTN-2基因的序列分析还揭示了第一个内含子的多态性,鉴定了三个等位基因。第一内含子的等位基因“ 1R”和“ 2R”的长度差异是由于存在于第一内含子的5'末端的一个或两个拷贝的大约150 bp的重复区块所致。第三个等位基因“ 4R”在第一个内含子3'端上游116 bp处有一个323 bp的额外插入。对几个DNA集合的分析表明,最常见的是“ 2R”等位基因,其次是“ 4R”等位基因,而“ 1R”等位基因则相对较少。全同胞家族的后代分析显示了两个遗传基因座的孟德尔遗传模式。在两个遗传标记和生长速率之间没有明确的关联。结论这些结果首次表明,在鲈形鱼类中,MSTN-2基因的启动子和第一内含子均具有相当程度的多态性,这表明进化过程中发生了染色体重排。

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