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蓝藻基因组中编码类真核信号蛋白的基因的调查、分析及基因组织

Survey, analysis and genetic organization of genes encoding eukaryotic-like signaling proteins on a cyanobacterial genome.

作者信息

Zhang C C, Gonzalez L, Phalip V

机构信息

Unité d'Immunotechnologie et Microbiologie Moléculaires, Ecole Supérieure de Biotechnologie de Strasbourg, Université Louis Pasteur de Strasbourg, Boulevard Sébastien Brandt, F-67400 Illkirch, France.

出版信息

Nucleic Acids Res. 1998 Aug 15;26(16):3619-25. doi: 10.1093/nar/26.16.3619.

Abstract

Bacteria usually use two-component systems for signal transduction, while eukaryotic organisms employ Ser/Thr and Tyr kinases and phosphatases for the same purpose. Many prokaryotes turn out to harbor Ser/Thr and Tyr kinases, Ser/Thr and Tyr phosphatases, and their accessory components as well. The sequence determination of the genome of the cyanobacterium Synechocystis sp. strain PCC 6803 offers the possibility to survey the extent of such molecules in a prokaryotic organism. This cyanobacterium possesses seven Ser/Thr kinases, seven Ser/Thr and Tyr phosphatases, one protein kinase interacting protein, one protein kinase regulatory subunit and several WD40-repeat-containing proteins. The majority of the protein phosphatases presented in this study were previously reported as hypothetical proteins. We analyze here the structure and genetic organization of these ORFs in the hope of providing a guidance for their functional analysis. Unlike their eukaryotic counterparts, many of these genes are clustered on the chromosome, and this genetic organization offers the opportunity to study their possible interaction. In several cases, genes of two-component transducers are found within the same cluster as those encoding a Ser/Thr kinase or a Ser/Thr phosphatase; the implication for signal transduction mechanism will be discussed.

摘要

细菌通常利用双组分系统进行信号转导,而真核生物则为此目的使用丝氨酸/苏氨酸激酶和酪氨酸激酶及磷酸酶。事实证明,许多原核生物也含有丝氨酸/苏氨酸激酶、酪氨酸激酶、丝氨酸/苏氨酸磷酸酶和酪氨酸磷酸酶及其辅助成分。蓝藻集胞藻PCC 6803菌株基因组序列的测定为研究原核生物中此类分子的存在程度提供了可能。这种蓝藻拥有7种丝氨酸/苏氨酸激酶、7种丝氨酸/苏氨酸和酪氨酸磷酸酶、1种蛋白激酶相互作用蛋白、1种蛋白激酶调节亚基以及几种含WD40重复序列的蛋白。本研究中呈现的大多数蛋白磷酸酶之前被报道为假定蛋白。我们在此分析这些开放阅读框的结构和基因组织,以期为其功能分析提供指导。与真核生物中的对应物不同,这些基因中的许多在染色体上成簇分布,这种基因组织为研究它们可能的相互作用提供了机会。在一些情况下,双组分传感器的基因与编码丝氨酸/苏氨酸激酶或丝氨酸/苏氨酸磷酸酶的基因位于同一簇中;将讨论其对信号转导机制的影响。

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