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蓝藻中的生物钟输入激酶及其同源物:进化约束与结构多样化。

Circadian input kinases and their homologs in cyanobacteria: evolutionary constraints versus architectural diversification.

机构信息

Institute of Genetics, National Academy of Sciences of Moldova, Chisinau, Moldova.

出版信息

J Mol Evol. 2010 May;70(5):453-65. doi: 10.1007/s00239-010-9344-0. Epub 2010 May 1.

Abstract

The circadian input kinase A (cikA) gene encodes a protein relaying environmental signal to the central circadian oscillator in cyanobacteria. The CikA protein has a variable architecture and usually consists of four tandemly arrayed domains: GAF, histidine kinase (HisKA), histidine kinase-like ATPase (HATPase_c), and a pseudo-receiver (REC). Among them, HisKA and HATPase_c are the least polymorphic, and REC is not present in heterocystic filamentous cyanobacteria. CikA contains several conserved motifs that are likely important for circadian function. There are at least three types of circadian systems, each of which possesses a different set of circadian genes. The originally described circadian system (kaiABC system) possesses both cikA and kaiA, while the others lack either only cikA (kaiABC (Delta)) or both (kaiBC). The results we obtained allowed us to approximate the time of the cikA origin to be about 2600-2200 MYA and the time of its loss in the species with the kaiABC (Delta) or kaiBC system between 1100 and 600 MYA. Circadian specialization of CikA, as opposed to its non-circadian homologs, is a result of several factors, including the unique conserved domain architecture and high evolutionary constraints of some domains and regions, which were previously identified as critical for the circadian function of the gene.

摘要

生物钟输入激酶 A(cikA)基因编码一种将环境信号传递给蓝藻中央生物钟振荡器的蛋白质。CikA 蛋白具有可变的结构,通常由四个串联排列的结构域组成:GAF、组氨酸激酶(HisKA)、组氨酸激酶样 ATP 酶(HATPase_c)和伪受体(REC)。其中,HisKA 和 HATPase_c 的多态性最小,而 REC 不存在于异形丝状体蓝藻中。CikA 包含几个保守基序,这些基序可能对生物钟功能很重要。至少有三种类型的生物钟系统,每个系统都拥有不同的一组生物钟基因。最初描述的生物钟系统(kaiABC 系统)既拥有 cikA 又拥有 kaiA,而其他系统则只缺少 cikA(kaiABC(Delta))或两者都缺少(kaiBC)。我们的研究结果使我们能够估计 cikA 的起源时间约为 2600-2200 百万年前,而在具有 kaiABC(Delta)或 kaiBC 系统的物种中,cikA 的丢失时间约为 1100-600 百万年前。与非生物钟同源物相反,CikA 的生物钟专业化是几个因素的结果,包括独特的保守结构域结构以及一些结构域和区域的高进化约束,这些结构域和区域以前被认为是基因生物钟功能的关键。

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