{"title":"Parasitic plasmids are anchored to inactive regions of eukaryotic chromosomes through a nucleosome signal.","authors":"Fabien Girard, Antoine Even, Agnès Thierry, Myriam Ruault, Léa Meneu, Pauline Larrous, Mickaël Garnier, Sandrine Adiba, Angela Taddei, Romain Koszul, Axel Cournac","doi":"10.1038/s44318-025-00389-1","DOIUrl":null,"url":null,"abstract":"<p><p>Natural plasmids are common in prokaryotes, but few have been documented in eukaryotes. The natural 2µ plasmid present in the yeast Saccharomyces cerevisiae is one of these best-characterized exceptions. This highly stable genetic element has coexisted with its host for millions of years, faithfully segregating at each cell division through a mechanism that remains unclear. Using proximity ligation methods (such as Hi-C, Micro-C) to map the contacts between 2µ plasmid and yeast chromosomes under dozens of different biological conditions, we found that the plasmid is tethered preferentially to regions with low transcriptional activity, often corresponding to long, inactive genes. These contacts do not depend on common chromosome-structuring factors, such as members of the structural maintenance of chromosome complexes (SMC) but depend on a nucleosome-encoded signal associated with RNA Pol II depletion. They appear stable throughout the cell cycle and can be established within minutes. This chromosome hitchhiking strategy may extend beyond the 2µ plasmid/S. cerevisiae pair, as suggested by the binding pattern of the natural eukaryotic plasmid Ddp5 along silent chromosome regions of the amoeba Dictyostelium discoideum.</p>","PeriodicalId":50533,"journal":{"name":"EMBO Journal","volume":" ","pages":"2134-2156"},"PeriodicalIF":8.3000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11962162/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EMBO Journal","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s44318-025-00389-1","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Natural plasmids are common in prokaryotes, but few have been documented in eukaryotes. The natural 2µ plasmid present in the yeast Saccharomyces cerevisiae is one of these best-characterized exceptions. This highly stable genetic element has coexisted with its host for millions of years, faithfully segregating at each cell division through a mechanism that remains unclear. Using proximity ligation methods (such as Hi-C, Micro-C) to map the contacts between 2µ plasmid and yeast chromosomes under dozens of different biological conditions, we found that the plasmid is tethered preferentially to regions with low transcriptional activity, often corresponding to long, inactive genes. These contacts do not depend on common chromosome-structuring factors, such as members of the structural maintenance of chromosome complexes (SMC) but depend on a nucleosome-encoded signal associated with RNA Pol II depletion. They appear stable throughout the cell cycle and can be established within minutes. This chromosome hitchhiking strategy may extend beyond the 2µ plasmid/S. cerevisiae pair, as suggested by the binding pattern of the natural eukaryotic plasmid Ddp5 along silent chromosome regions of the amoeba Dictyostelium discoideum.
天然质粒在原核生物中很常见,但在真核生物中很少有记录。存在于酵母中的天然2µ质粒是这些最具特征的例外之一。这种高度稳定的遗传元素已经与宿主共存了数百万年,在每次细胞分裂时都通过一种尚不清楚的机制忠实地分离。利用近距离连接方法(如Hi-C, Micro-C)绘制了数十种不同生物学条件下2µ质粒与酵母染色体之间的接触图谱,我们发现质粒优先被拴在转录活性低的区域,通常对应于长而无活性的基因。这些接触不依赖于常见的染色体结构因子,如染色体复合体(SMC)的结构维持成员,而是依赖于与RNA Pol II耗尽相关的核小体编码信号。它们在整个细胞周期中表现稳定,可以在几分钟内建立起来。这种染色体搭便车策略可能超过2µ质粒/S。根据天然真核质粒Ddp5在阿米巴Dictyostelium disideum的沉默染色体区域的结合模式,可以推测出这对染色体。
期刊介绍:
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