Sverdlov E D
Institute of Molecular Genetics, USSR Academy of Sciences, Moscow.
Genetica. 1991;85(1):91-101. doi: 10.1007/BF00056110.
The review is devoted to analysis of research carried out in the author's laboratory on structure-function relationships in genes coding for Na,K-ATPases. Also considered are problems related to molecular evolution of ion-transporting ATPases. This brief review is devoted to a fragment of research carried out in my laboratory, the Laboratory of Human Genes Structure and Function at the Shemyakin Institute of Bioorganic Chemistry, USSR Academy of Sciences. The area of the review may be named as structural-evolutionary analysis of functional anatomies of genes. The approach is fairly standard and its essence was formulated long ago: evolution decides 'to be or not to be' based on usefulness or lack of it. The elements of genes that are important for the gene function are retained in the course of evolution, and a comparison of genes having similar functions in different species should, hopefully, reveal different behavior of gene blocks, conservation of functionally significant blocks and variability of less significant or insignificant ones. An approach like this has been widely used in comparing proteins. However, a study of genes gives the investigator yet another tool of structural and evolutionary import: the exon structure may be relevant to the gene's evolutionary history, with exons corresponding to the functional domains (arguments for and against this fascinating hypothesis have been reviewed by Blake (Blake, 1985). However, even if the exon-domain correlation does not hold in the general case, a similarity in the exon-intron pattern of genes from different species is indicative of their common evolutionary origin and is enforcing the logic of variability analysis, provided, of course, that the compared genes have a common predecessor. A few years ago we employed this approach to analyze the functional structure of genes coding for subunits of bacterial DNA-dependent RNA polymerases and constructed functional maps of the enzyme. After that, a similar study of Na,K-ATPase genes to be reviewed here was started. The entire project became possible through collaboration with the lab of Dr. N. N. Modyanov, an eminent specialist in protein chemistry who had already accumulated considerable information on Na,K-ATPase from pig kidneys by that time. I would also like to stress that the work has been started on the initiative of the deceased Director of the Institute, Yu. A. Ovchinnikov. Since this is a self-review, I am asking my colleagues whose work will not be cited here to excuse me.(ABSTRACT TRUNCATED AT 400 WORDS)
这篇综述致力于分析作者所在实验室关于编码钠钾ATP酶的基因结构与功能关系的研究。同时也探讨了与离子转运ATP酶分子进化相关的问题。这篇简短的综述聚焦于我所在实验室(苏联科学院谢马亚金生物有机化学研究所人类基因结构与功能实验室)开展的部分研究。综述的领域可称为基因功能解剖的结构进化分析。该方法相当标准,其核心早在很久以前就已阐明:进化基于有用性与否来决定“生存还是毁灭”。基因中对基因功能重要的元件在进化过程中得以保留,比较不同物种中具有相似功能的基因,有望揭示基因片段的不同行为、功能重要片段的保守性以及不太重要或无足轻重片段的变异性。这样的方法已广泛用于比较蛋白质。然而,对基因的研究为研究者提供了另一个具有结构和进化意义的工具:外显子结构可能与基因的进化史相关,外显子对应于功能结构域(布莱克(Blake,1985)已对支持和反对这一迷人假说的论据进行了综述)。然而,即便外显子 - 结构域的相关性在一般情况下不成立,不同物种基因的外显子 - 内含子模式的相似性表明它们有共同的进化起源,并且强化了变异性分析的逻辑性,当然前提是所比较的基因有共同的祖先。几年前我们采用这种方法分析了编码细菌DNA依赖性RNA聚合酶亚基的基因的功能结构,并构建了该酶的功能图谱。之后,便开始了这里要综述的钠钾ATP酶基因的类似研究。整个项目得以开展得益于与N. N. 莫佳诺夫博士实验室的合作,他是蛋白质化学领域的杰出专家,当时已经积累了关于猪肾钠钾ATP酶的大量信息。我还要强调,这项工作是在已故的研究所所长尤·阿·奥夫钦尼科夫的倡议下启动的。由于这是一篇自我综述,我请求那些工作未在此处被引用的同事谅解。(摘要截选至400字)