Suppr超能文献

真核生物中的多顺反子肽编码基因——它们有多普遍?

Polycistronic peptide coding genes in eukaryotes--how widespread are they?

作者信息

Tautz Diethard

机构信息

Max-Planck-Institut für Evolutionsbiologie, August-Thienemannstrasse 2, Plön, Germany.

出版信息

Brief Funct Genomic Proteomic. 2009 Jan;8(1):68-74. doi: 10.1093/bfgp/eln054. Epub 2008 Dec 12.

Abstract

The classical textbook assumption for the structure of an eukaryotic gene is that it codes for a single polypeptide of more than 100 amino acids in length. This is also the implicit assumption in most gene annotation pipelines. A gene family has now been discovered in insects that shows that an eukaryotic mRNA can code for peptides as short as eleven amino acids and that a single mRNA can code for several such peptides. This raises the question whether short open reading frames might also have a functional potential in other mRNAs, in particular those that occur in the 5'-UTR of many mRNAs. A number of these have been shown to act in cis to regulate the translation of the main open reading frame of the mRNA. But there may be others that could act in trans on other biological processes. The question of how many peptide-coding genes may exist is therefore worth revisiting. This poses new bioinformatic challenges that can only be resolved through multiple genome comparisons within a range of evolutionary distances.

摘要

关于真核基因结构的经典教科书假设是,它编码一条长度超过100个氨基酸的单一多肽。这也是大多数基因注释流程中的隐含假设。现在在昆虫中发现了一个基因家族,该家族表明真核mRNA可以编码短至11个氨基酸的肽,并且单个mRNA可以编码几种这样的肽。这就提出了一个问题,即短开放阅读框在其他mRNA中是否也可能具有功能潜力,特别是那些存在于许多mRNA的5'-UTR中的短开放阅读框。其中一些已被证明在顺式作用中调节mRNA主要开放阅读框的翻译。但可能还有其他一些短开放阅读框可以在反式作用中作用于其他生物学过程。因此,关于可能存在多少个肽编码基因的问题值得重新审视。这带来了新的生物信息学挑战,只有通过在一系列进化距离内进行多个基因组比较才能解决。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验