类Pif1解旋酶在维持基因组稳定性中的作用。
Roles of Pif1-like helicases in the maintenance of genomic stability.
作者信息
Boulé Jean-Baptiste, Zakian Virginia A
机构信息
Department of Molecular Biology, Lewis Thomas Laboratories, Princeton University, Princeton, NJ 08544, USA.
出版信息
Nucleic Acids Res. 2006;34(15):4147-53. doi: 10.1093/nar/gkl561. Epub 2006 Aug 25.
The Pif1p family of DNA helicases is conserved from yeast to humans. To date, four members of this family have been analyzed in some detail by in vitro and in vivo assays: the two baker's yeast helicases, ScPif1p and Rrm3p, the fission yeast Pfh1p and the human enzyme hPif1p. In vitro, these enzymes are 5' to 3' DNA helicase and show little processivity. In vivo, ScPif1p, Rrm3p and probably Pfh1p, function in both the nucleus at specific genomic loci and in mitochondria, where they are needed for the stable maintenance of the genome as accessory helicases to the replication machinery. Interestingly, they act on common DNA substrates but appear to have largely non-overlapping cellular functions, ranging from Okazaki fragment processing, telomerase inhibition, to helping the replication fork progress through non-nucleosomal protein-DNA complexes. For example, both ScPif1p and Rrm3p affect the replication of telomeres, but in a different way: Pif1p inhibits telomerase-mediated telomere elongation by directly removing telomerase from a DNA end, whereas Rrm3p facilitates replication through telomeric DNA. Here we review the current knowledge on the Pif1-like helicases, as a first step towards understanding the basis of their functional specialization and mechanism of action.
DNA解旋酶的Pif1p家族在从酵母到人类的生物中都保守存在。迄今为止,该家族的四个成员已通过体外和体内试验进行了一些详细分析:两种酿酒酵母解旋酶,即ScPif1p和Rrm3p,裂殖酵母的Pfh1p以及人类酶hPif1p。在体外,这些酶是5'至3'DNA解旋酶,且持续性较差。在体内,ScPif1p、Rrm3p以及可能的Pfh1p,在细胞核内特定基因组位点和线粒体中均发挥作用,在这些地方它们作为复制机器的辅助解旋酶,对于基因组的稳定维持是必需的。有趣的是,它们作用于共同的DNA底物,但似乎具有很大程度上不重叠的细胞功能,范围从冈崎片段加工、端粒酶抑制到帮助复制叉通过非核小体蛋白-DNA复合物。例如,ScPif1p和Rrm3p都影响端粒的复制,但方式不同:Pif1p通过直接从DNA末端去除端粒酶来抑制端粒酶介导的端粒延长,而Rrm3p则促进通过端粒DNA的复制。在此,我们综述关于Pif1样解旋酶的当前知识,作为理解其功能特化基础和作用机制的第一步。