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人猿超科中与生殖相关的TMEM30C转录本的异常终止。

Aberrant termination of reproduction-related TMEM30C transcripts in the hominoids.

作者信息

Osada Naoki, Hashimoto Katsuyuki, Hirai Momoki, Kusuda Jun

机构信息

Division of Biomedical Research Resources, National Institute of Biomedical Innovation, 7-6-8 Saito-Asagi, Ibaraki, Osaka 567-0085, Japan.

出版信息

Gene. 2007 May 1;392(1-2):151-6. doi: 10.1016/j.gene.2006.11.021. Epub 2006 Dec 12.

DOI:10.1016/j.gene.2006.11.021
PMID:17258408
Abstract

Finding genetic novelties that may contribute to human-specific physiology and diseases is a key issue of current biomedical studies. TMEM30C is a gene containing two transmembrane (TM) domains and homologous to the yeast CDC50 family, which is related to polarized cell division. It is conserved among mammals along with two other paralogs, TMEM30A and TMEM30B. We found that TMEM30C is expressed specifically in the testis of mammals, in contrast to the relatively wide expression distributions of the other paralogs. While macaques expressed two alternative splicing isoforms which include one or two TM domains, humans and chimpanzees predominantly expressed truncated transcripts because of the mutations in the splicing and/or poly(A) signal sites. The major transcript in humans harbored non-stop ORF (open reading frame) while the chimpanzee counterpart encoded a protein with one TM domain. The difference was due to the 1-bp indel upstream of the poly(A) signal site. In addition, both the hominoids expressed minor transcripts encoding short proteins with one TM domain. Phylogenetic analysis has showed the acceleration of amino acid substitution after the human and chimpanzee divergence, which may have been caused by a recent relaxation in functional constraints or positive selection on TMEM30C. Elucidating the precise reproductive function of TMEM30C in mammals will be important to the foundation of divergence in higher primates at a molecular level.

摘要

寻找可能导致人类特异性生理和疾病的遗传新特性是当前生物医学研究的关键问题。跨膜蛋白30C(TMEM30C)是一个含有两个跨膜结构域的基因,与酵母CDC50家族同源,该家族与细胞极性分裂有关。它与另外两个旁系同源物跨膜蛋白30A(TMEM30A)和跨膜蛋白30B(TMEM30B)在哺乳动物中保守。我们发现,与其他旁系同源物相对广泛的表达分布不同,TMEM30C在哺乳动物的睾丸中特异性表达。猕猴表达两种可变剪接异构体,其中包括一个或两个跨膜结构域,而人类和黑猩猩由于剪接和/或聚腺苷酸化信号位点的突变,主要表达截短的转录本。人类的主要转录本含有不间断开放阅读框(ORF),而黑猩猩的对应物编码一种含有一个跨膜结构域的蛋白质。这种差异是由于聚腺苷酸化信号位点上游1个碱基的插入缺失。此外,类人猿都表达编码具有一个跨膜结构域的短蛋白的次要转录本。系统发育分析表明,人类和黑猩猩分化后氨基酸替代加速,这可能是由于最近TMEM30C的功能限制放松或正选择所致。阐明TMEM30C在哺乳动物中的精确生殖功能对于从分子水平理解高等灵长类动物的分化基础至关重要。

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