首页> 外文期刊>G3: Genes, Genomes, Genetics >Functional Conservation of the Pre-Sensor One Beta-Finger Hairpin (PS1-hp) Structures in Mini-Chromosome Maintenance Proteins of Saccharomyces cerevisiae and Archaea
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Functional Conservation of the Pre-Sensor One Beta-Finger Hairpin (PS1-hp) Structures in Mini-Chromosome Maintenance Proteins of Saccharomyces cerevisiae and Archaea

机译:酿酒酵母和古细菌的微型染色体维持蛋白中的传感器前一个β手指发夹(PS1-hp)结构的功能性保守。

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Mini-chromosome maintenance (MCM) proteins form complexes that are required for DNA replication and are highly conserved throughout evolution. The replicative helicase of eukaryotic organisms is composed of the six paralogs MCM2-7 , which form a heterohexameric ring structure. In contrast, the structure of the archaean replicative MCM helicase is a single Mcm protein that forms a homohexameric complex. Atomic structures of archaeal MCMs have identified multiple beta-finger structures in Mcm proteins whose in vivo function is unknown. In the present study, we have investigated the physiological role of the pre-sensor 1 beta - hairpin (PS1-hp) beta-fingers of Saccharomyces cerevisiae [Mcm4p][1] and [Mcm5p][2] in DNA replication initiation and elongation in vivo . The PS1-hp beta-finger mutant of [Mcm5p][2] ( [mcm5][2]-HAT K506A :: [URA3][3] ) has a growth defect at both 18° and 37°. Mutation of the [Mcm4p][1] PS1-hp beta-finger ( [mcm4][1]-HA K658A :: [TRP1][4] ) does not have a growth defect, indicating different functional contributions of the PS1-hp beta-finger structures of different MCM helicase subunits. Both [Mcm4p][1] and [Mcm5p][2] PS1-hp beta-finger mutants can coimmunoprecipitate [Mcm2p][5], indicating the formation of the hexameric MCM helicase complex. Both PS1-hp beta-finger mutants have a plasmid loss phenotype that is suppressible by origin dosage, indicating a defective replication initiation. Surprisingly, a defect in the binding of PS1-hp MCM mutants to origins of DNA replication was not found by chromatin immunoprecipitation, suggesting a novel interpretation in which the defect is in a subsequent step of DNA strand separation by the MCM helicase. The double mutant [mcm4][1]-HA K658A :: [TRP1][4] [mcm5][2]-HAT K506A :: [URA3][3] is lethal, displaying a terminal MCM mutant phenotype of large budded cells. [1]: http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid=S000006223 [2]: http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid=S000004264 [3]: http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid=S000000747 [4]: http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid=S000002414 [5]: http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid=S000000119.
机译:微型染色体维持(MCM)蛋白形成DNA复制所需的复合物,并且在整个进化过程中高度保守。真核生物的复制解旋酶由六个异源MCM2-7组成,它们形成异六聚体环结构。相反,古细菌复制性MCM解旋酶的结构是形成同六聚体复合物的单个Mcm蛋白。古细菌MCM的原子结构已在Mcm蛋白中鉴定出多个β指结构,其体内功能未知。在本研究中,我们研究了酿酒酵母[Mcm4p] [1]和[Mcm5p] [2]的前传感器1β-发夹(PS1-hp)β-指在DNA复制起始和延伸中的生理作用。体内。 [Mcm5p] [2]([mcm5] [2] -HAT K506A :: [URA3] [3])的PS1-hp beta-finger突变体在18°和37°都有生长缺陷。 [Mcm4p] [1] PS1-hpβ指的突变([mcm4] [1] -HA K658A :: [TRP1] [4])没有生长缺陷,表明PS1-hp的功能不同MCM解旋酶亚基的β-指结构。 [Mcm4p] [1]和[Mcm5p] [2] PS1-hp beta-finger突变体都可以共免疫沉淀[Mcm2p] [5],表明六聚体MCM解旋酶复合物的形成。两种PS1-hpβ-手指突变体均具有可通过来源剂量抑制的质粒缺失表型,表明复制起始有缺陷。出乎意料的是,染色质免疫沉淀法未发现PS1-hp MCM突变体与DNA复制起点的结合缺陷,这提示了一种新的解释,其中该缺陷在于MCM解旋酶分离DNA链的后续步骤。双重突变体[mcm4] [1] -HA K658A :: [TRP1] [4] [mcm5] [2] -HAT K506A :: [URA3] [3]具有致死性,显示出大芽细胞的终末MCM突变表型。 。 [1]:http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid = S000006223 [2]:http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid = S000004264 [3]:http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid = S000000747 [4]:http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid = S000002414 [5]:http://www.yeastgenome.org/cgi-bin/locus.fpl?dbid = S000000119。

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