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Divisome and segrosome components of Deinococcus radiodurans interact through cell division regulatory proteins

机译:放射球菌的Didivsome和segrosome成分通过细胞分裂调节蛋白相互作用

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The Deinococcus radiodurans genome encodes many of the known components of divisome as well as four sets of genome partitioning proteins, ParA and ParB on its multipartite genome. Interdependent regulation of cell division and genome segregation is not understood. In vivo interactions of D. radiodurans' sdivisome, segrosome and other cell division regulatory proteins expressed on multicopy plasmids were studied in Escherichia coli using a bacterial two-hybrid system and confirmed by co-immunoprecipitation with the proteins made in E. coli. Many of these showed interactions both with the self and with other proteins. For example, DrFtsA, DrFtsZ, DrMinD, DrMinC, DrDivIVA and all four ParB proteins individually formed at least homodimers, while DrFtsA interacted with DrFtsZ, DrFtsW, DrFtsE, DrFtsK and DrMinD. DrMinD also showed interaction with DrFtsW, DrFtsE and DrMinC. Interestingly, septum site determining protein, DrDivIVA showed interactions with secondary genome ParAs as well as ParB1, ParB3 and ParB4 while DrMinC interacted with ParB1 and ParB3. PprA, a pleiotropic protein recently implicated in cell division regulation, neither interacted with divisome proteins nor ParBs but interacted at different levels with all four ParAs. These results suggest the formation of independent multiprotein complexes of ‘DrFts’ proteins, segrosome proteins and cell division regulatory proteins, and these complexes could interact with each other through DrMinC and DrDivIVA, and PprA in D. radiodurans.
机译:辐射球菌的基因组编码了许多已知的组成部分,以及其多部分基因组上的四组基因组分配蛋白,即ParA和ParB。细胞分裂和基因组分离的相互依存调节尚不清楚。 D. radiodurans的体内相互作用在多拷贝质粒上表达的sdivisome,segrosome和其他细胞分裂调节蛋白在细菌中使用细菌两杂交系统在大肠杆菌中进行了研究,并与大肠杆菌中的蛋白进行了共免疫沉淀法得到证实。其中许多表现出与自身以及与其他蛋白质的相互作用。例如,DrFtsA,DrFtsZ,DrMinD,DrMinC,DrDivIVA和所有四种ParB蛋白分别形成至少同二聚体,而DrFtsA与DrFtsZ,DrFtsW,DrFtsE,DrFtsK和DrMinD相互作用。 DrMinD还显示了与DrFtsW,DrFtsE和DrMinC的交互。有趣的是,间隔位点决定蛋白DrDivIVA显示与次级基因组ParAs以及ParB1,ParB3和ParB4相互作用,而DrMinC与ParB1和ParB3相互作用。 PprA是一种多效性蛋白,最近与细胞分裂调控有关,既不与divisome蛋白也不与ParBs相互作用,但与所有四个ParA都以不同的水平相互作用。这些结果表明,“ DrFts”蛋白,脂质体蛋白和细胞分裂调节蛋白形成了独立的多蛋白复合物,这些复合物可以通过DrMinC和DrDivIVA以及PduA在放射杜鹃中相互相互作用。

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