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酵母 2 微米质粒蛋白 Rep1 和 Rep2 的 sumoylation 缺陷与它们从质粒分配区域的丢失以及质粒遗传受损有关。

Deficient sumoylation of yeast 2-micron plasmid proteins Rep1 and Rep2 associated with their loss from the plasmid-partitioning locus and impaired plasmid inheritance.

机构信息

Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

PLoS One. 2013;8(3):e60384. doi: 10.1371/journal.pone.0060384. Epub 2013 Mar 28.

DOI:10.1371/journal.pone.0060384
PMID:23555963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3610928/
Abstract

The 2-micron plasmid of the budding yeast Saccharomyces cerevisiae encodes copy-number amplification and partitioning systems that enable the plasmid to persist despite conferring no advantage to its host. Plasmid partitioning requires interaction of the plasmid Rep1 and Rep2 proteins with each other and with the plasmid-partitioning locus STB. Here we demonstrate that Rep1 stability is reduced in the absence of Rep2, and that both Rep proteins are sumoylated. Lysine-to-arginine substitutions in Rep1 and Rep2 that inhibited their sumoylation perturbed plasmid inheritance without affecting Rep protein stability or two-hybrid interaction between Rep1 and Rep2. One-hybrid and chromatin immunoprecipitation assays revealed that Rep1 was required for efficient retention of Rep2 at STB and that sumoylation-deficient mutants of Rep1 and Rep2 were impaired for association with STB. The normal co-localization of both Rep proteins with the punctate nuclear plasmid foci was also lost when Rep1 was sumoylation-deficient. The correlation of Rep protein sumoylation status with plasmid-partitioning locus association suggests a theme common to eukaryotic chromosome segregation proteins, sumoylated forms of which are found enriched at centromeres, and between the yeast 2-micron plasmid and viral episomes that depend on sumoylation of their maintenance proteins for persistence in their hosts.

摘要

酿酒酵母芽殖酵母的 2 微米质粒编码复制数扩增和分区系统,使质粒能够在不赋予宿主任何优势的情况下持续存在。质粒分区需要质粒 Rep1 和 Rep2 蛋白相互作用,以及与质粒分区位点 STB 相互作用。在这里,我们证明在没有 Rep2 的情况下,Rep1 的稳定性降低,并且两个 Rep 蛋白都被 SUMO 化。抑制 Rep1 和 Rep2 的 SUMO 化的赖氨酸到精氨酸取代会干扰质粒遗传,而不影响 Rep 蛋白稳定性或 Rep1 和 Rep2 之间的双杂交相互作用。单杂交和染色质免疫沉淀分析表明,Rep1 对于 Rep2 在 STB 处的有效保留是必需的,并且 Rep1 和 Rep2 的 SUMO 化缺陷突变体与 STB 的关联受到损害。当 Rep1 缺乏 SUMO 化时,两个 Rep 蛋白与点状核质粒焦点的正常共定位也丢失了。Rep 蛋白 SUMO 化状态与质粒分区位点关联的相关性表明了一种常见于真核染色体分离蛋白的主题,其 SUMO 化形式在着丝粒处富集,并且在酵母 2 微米质粒和依赖于其维持蛋白 SUMO 化的病毒附加体中发现,以维持在其宿主中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/3610928/c76f9a5b6e19/pone.0060384.g008.jpg
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