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首页> 外文期刊>Nucleic Acids Research >Structure-function relationships of two paralogous single-stranded DNA-binding proteins from Streptomyces coelicolor: implication of SsbB in chromosome segregation during sporulation
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Structure-function relationships of two paralogous single-stranded DNA-binding proteins from Streptomyces coelicolor: implication of SsbB in chromosome segregation during sporulation

机译:Coelicolor链霉菌的两个旁系单链DNA结合蛋白的结构功能关系:孢子形成过程中SsbB在染色体分离中的意义

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The linear chromosome of Streptomyces coelicolor contains two paralogous ssb genes, ssbA and ssbB. Following mutational analysis, we concluded that ssbA is essential, whereas ssbB plays a key role in chromosome segregation during sporulation. In the ssbB mutant, —30% of spores lacked DNA. The two ssb genes were expressed differently; in minimal medium, gene expression was prolonged for both genes and significantly upregulated for ssbB. The ssbA gene is transcribed as part of a polycistronic mRNA from two initiation sites, 163 bp and 75 bp upstream of the rpsF translational start codon. The ssbB gene is transcribed as a monocistronic mRNA, from an unusual promoter region, 73 bp upstream of the AUG codon. Distinctive DNA-binding affinities of single-stranded DNA-binding proteins monitored by tryptophan fluorescent quenching and electrophoretic mobility shift were observed. The crystal structure of SsbB at 1.7 A resolution revealed a common OB-fold, lack of the clamp-like structure conserved in SsbAand previously unpublished S-S bridges between the A/B and C/D subunits. This is the first report of the determination of paralogous singlestranded DNA-binding protein structures from the same organism. Phylogenetic analysis revealed frequent duplicationof ssb genes in Actinobacteria, whereas their strong retention suggests that they are involved in important cellular functions.
机译:天蓝色链霉菌的线性染色体包含两个同源的ssb基因,ssbA和ssbB。经过突变分析,我们得出结论,ssbA是必不可少的,而ssbB在孢子形成过程中的染色体分离中起着关键作用。在ssbB突变体中,约30%的孢子缺乏DNA。两种ssb基因的表达不同。在基本培养基中,两个基因的基因表达均延长,而ssbB则明显上调。 ssbA基因作为多顺反子mRNA的一部分从rpsF翻译起始密码子上游的163 bp和75 bp的两个起始位点转录。 ssbB基因以单顺反子mRNA的形式转录,来自AUG密码子上游73 bp的异常启动子区域。观察到通过色氨酸荧光猝灭和电泳迁移率迁移监测的单链DNA结合蛋白的独特DNA结合亲和力。 SsbB的晶体结构在1.7 A分辨率下显示出常见的OB折叠,缺乏SsbA中保守的钳状结构以及A / B和C / D亚基之间以前未公开的S-S桥。这是确定同一生物的旁源单链DNA结合蛋白结构的第一份报告。系统发育分析表明,放线菌中ssb基因经常重复,而它们的强烈保留表明它们参与重要的细胞功能。

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