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首页> 外文期刊>Zoologia (Curitiba) >Molecular cloning and analysis of Myc modulator 1 (Mm-1) from Bufo gargarizans (Amphibia: Anura)
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Molecular cloning and analysis of Myc modulator 1 (Mm-1) from Bufo gargarizans (Amphibia: Anura)

机译:中华蟾蜍(两栖动物:阿努拉)Myc调节剂1(Mm-1)的分子克隆和分析

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The protein of Myc modulator 1 (Mm-1) has been reported to repress the transcriptional activity of the proto-oncogene c-Myc in humans. Moreover, it was shown to be the subunit 5 of human prefoldin (PFD). So far, this gene and its homologs have been isolated and sequenced in many organisms, such as mammals and fish, but has not been sequenced for any amphibian or reptile. In order to better understand the function and evolution of Mm-1, we isolated a full-length Mm-1 cDNA (BgMm-1, GenBank accession no. EF211947) from Bufo gargarizans (Cantor, 1842) using RACE (rapid amplification of cDNA ends) methods. Mm-1 in B. gargarizans is 755 bp long, comprising an open reading frame (ORF) of 459 bp encoding 152 amino acids. The amino acid sequence had a prefoldin α-like domain, partially including a typical putative leucine zipper motif. BgMm-1 showed high similarity to its homolog of Mus musculus Linnaeus, 1758 (82%) and Homo sapiens Linnaeus, 1758 MM-1 isoform a (81%) at the amino acid level. The protein secondary structure modeled with the SWISS MODEL server revealed that there were two α-helices and four b-strands in BgMm-1 as its human orthologue, and both proteins belonged to the a class of PFD family. The phylogenetic relationships of Mm-1s from lower archaea to high mammals was consistent with the evolution of species, meanwhile the cluster result was consistent with the multiple alignment and the sequence identity analysis. RT-PCR (reverse transcriptase-polymerase chain reaction) analysis demonstrated that BgMm-1 expressed widely in ten tissues of adult toad. These results can be helpful for the further investigation on the evolution of Mm-1.
机译:据报道,Myc调节剂1(Mm-1)的蛋白质可抑制人类原癌基因c-Myc的转录活性。此外,它被证明是人类前折叠蛋白(PFD)的亚基5。迄今为止,该基因及其同源物已在许多生物体中分离并测序,例如哺乳动物和鱼类,但尚未对任何两栖动物或爬行动物进行测序。为了更好地了解Mm-1的功能和进化,我们使用RACE(快速扩增cDNA)从Bufo gargarizans(Cantor,1842)分离了全长Mm-1 cDNA(BgMm-1,GenBank登录号EF211947)。结束)方法。 gar。gargarizans中的Mm-1长755 bp,包含459 bp的开放阅读框(ORF),编码152个氨基酸。氨基酸序列具有前折叠蛋白α样结构域,部分包括典型的假定的亮氨酸拉链基序。 BgMm-1在氨基酸水平上与小家鼠1758(82%)和智人1758 MM-1亚型a(81%)的同系物表现出高度相似性。用SWISS MODEL服务器建模的蛋白质二级结构显示BgMm-1中有两个α螺旋和四个b链作为人类直系同源物,并且这两个蛋白质都属于PFD家族一类。 Mm-1s从下古细菌到高等哺乳动物的系统发育关系与物种进化一致,而聚类结果与多重比对和序列同一性分析一致。 RT-PCR(逆转录聚合酶链反应)分析表明,BgMm-1在成年蟾蜍的十个组织中广泛表达。这些结果可能有助于进一步研究Mm-1的进化。

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