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后生动物早期进化过程中 Pak 原癌基因的功能转变。

Functional transition of Pak proto-oncogene during early evolution of metazoans.

机构信息

Department of Oncogene Research, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.

出版信息

Oncogene. 2010 Jul 1;29(26):3815-26. doi: 10.1038/onc.2010.148. Epub 2010 May 10.

Abstract

Proto-oncogenes encode signaling molecular switches regulating cellular homeostasis in metazoans, and can be converted to oncogenes by gain-of-function mutations. To address the molecular basis for development of the regulatory system of proto-oncogenes during evolution, we screened for ancestral proto-oncogenes from the unicellular choanoflagellate Monosiga ovata by monitoring their transforming activities, and isolated a Pak gene ortholog encoding a serine/threonine kinase as a 'primitive oncogene'. We also cloned Pak orthologs from fungi and the multicellular sponge Ephydatia fluviatilis, and compared their regulatory features with that of M. ovata Pak (MoPak). MoPak is constitutively active and induces cell transformation in mammalian fibroblasts, although the Pak orthologs from multicellular animals are strictly regulated. Analyses of Pak mutants revealed that structural alteration of the auto-inhibitory domain (AID) of MoPak confers higher constitutive kinase activity, as well as greater binding ability to Rho family GTPases than the multicellular Paks, and this structural alteration is responsible for cell transformation and disruption of multicellular tissue organization. These results show that maturation of AID function was required for the development of the strict regulatory system of the Pak proto-oncogene, and suggest a potential link between the establishment of the regulatory system of proto-oncogenes and metazoan evolution.

摘要

原癌基因编码信号分子开关,调节后生动物细胞的内稳态,并且可以通过获得功能突变转化为癌基因。为了解析原癌基因调控系统在进化过程中分子基础,我们通过监测转化活性,从单细胞领鞭毛虫(Monosiga ovata)中筛选出祖先原癌基因,并分离出编码丝氨酸/苏氨酸激酶的 Pak 基因同源物作为“原始癌基因”。我们还从真菌和多细胞海绵(Ephydatia fluviatilis)中克隆了 Pak 同源物,并比较了它们与 M. ovata Pak(MoPak)的调控特征。MoPak 是组成型激活的,可诱导哺乳动物成纤维细胞转化,尽管来自多细胞动物的 Pak 同源物受到严格调控。Pak 突变体的分析表明,MoPak 自动抑制结构域(AID)的结构改变赋予了更高的组成型激酶活性,以及比多细胞 Paks 更高的 Rho 家族 GTPases 结合能力,这种结构改变负责细胞转化和破坏多细胞组织的结构。这些结果表明,AID 功能的成熟是 Pak 原癌基因严格调控系统发育所必需的,并提示原癌基因调控系统的建立与后生动物进化之间存在潜在联系。

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