Schmelling Nicolas M, Lehmann Robert, Chaudhury Paushali, Beck Christian, Albers Sonja-Verena, Axmann Ilka M, Wiegard Anika
Institute for Synthetic Microbiology, Cluster of Excellence on Plant Sciences (CEPLAS), Heinrich Heine University Duesseldorf, Universitaetsstrasse 1, Duesseldorf, 40225, Germany.
Institute for Theoretical Biology, Humboldt University Berlin, Invalidenstrasse 43, Berlin, 10115, Germany.
BMC Evol Biol. 2017 Jul 21;17(1):169. doi: 10.1186/s12862-017-0999-7.
Circadian clocks are found in organisms of almost all domains including photosynthetic Cyanobacteria, whereby large diversity exists within the protein components involved. In the model cyanobacterium Synechococcus elongatus PCC 7942 circadian rhythms are driven by a unique KaiABC protein clock, which is embedded in a network of input and output factors. Homologous proteins to the KaiABC clock have been observed in Bacteria and Archaea, where evidence for circadian behavior in these domains is accumulating. However, interaction and function of non-cyanobacterial Kai-proteins as well as homologous input and output components remain mainly unclear.
Using a universal BLAST analyses, we identified putative KaiC-based timing systems in organisms outside as well as variations within Cyanobacteria. A systematic analyses of publicly available microarray data elucidated interesting variations in circadian gene expression between different cyanobacterial strains, which might be correlated to the diversity of genome encoded clock components. Based on statistical analyses of co-occurrences of the clock components homologous to Synechococcus elongatus PCC 7942, we propose putative networks of reduced and fully functional clock systems. Further, we studied KaiC sequence conservation to determine functionally important regions of diverged KaiC homologs. Biochemical characterization of exemplary cyanobacterial KaiC proteins as well as homologs from two thermophilic Archaea demonstrated that kinase activity is always present. However, a KaiA-mediated phosphorylation is only detectable in KaiC1 orthologs.
Our analysis of 11,264 genomes clearly demonstrates that components of the Synechococcus elongatus PCC 7942 circadian clock are present in Bacteria and Archaea. However, all components are less abundant in other organisms than Cyanobacteria and KaiA, Pex, LdpA, and CdpA are only present in the latter. Thus, only reduced KaiBC-based or even simpler, solely KaiC-based timing systems might exist outside of the cyanobacterial phylum, which might be capable of driving diurnal oscillations.
几乎在所有生物域的生物体中都发现了生物钟,包括光合蓝细菌,其中涉及的蛋白质成分存在很大差异。在模式蓝细菌聚球藻PCC 7942中,昼夜节律由独特的KaiABC蛋白质生物钟驱动,该生物钟嵌入输入和输出因子网络中。在细菌和古菌中观察到了与KaiABC生物钟同源的蛋白质,这些生物域中昼夜行为的证据正在积累。然而,非蓝细菌Kai蛋白以及同源输入和输出成分的相互作用和功能仍主要不清楚。
通过通用的BLAST分析,我们在蓝细菌以外的生物体中鉴定出了假定的基于KaiC的计时系统以及蓝细菌内部的变异。对公开可用的微阵列数据进行系统分析,揭示了不同蓝细菌菌株之间昼夜节律基因表达的有趣差异,这可能与基因组编码的生物钟成分的多样性相关。基于对与聚球藻PCC 7942同源的生物钟成分共现情况的统计分析,我们提出了简化和功能完整的生物钟系统的假定网络。此外,我们研究了KaiC序列保守性,以确定分化的KaiC同源物的功能重要区域。对示例性蓝细菌KaiC蛋白以及来自两个嗜热古菌的同源物的生化特性分析表明,激酶活性始终存在。然而,仅在KaiC1直系同源物中可检测到KaiA介导的磷酸化。
我们对11264个基因组的分析清楚地表明,聚球藻PCC 7942生物钟的成分存在于细菌和古菌中。然而,所有成分在其他生物体中的丰度都低于蓝细菌,并且KaiA、Pex、LdpA和CdpA仅存在于后者中。因此,在蓝细菌门之外可能仅存在简化的基于KaiBC的计时系统,甚至可能存在更简单的仅基于KaiC的计时系统,它们可能能够驱动昼夜振荡。