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CUT&RUN 鉴定出罗伦隐球酵母IFO0880 的着丝粒 DNA 区域。

CUT&RUN identifies centromeric DNA regions of Rhodotorula toruloides IFO0880.

机构信息

Department of Chemical and Biomolecular Engineering, U.S. Department of Energy Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

Departments of Chemistry, Biochemistry, and Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

出版信息

FEMS Yeast Res. 2022 Jan 11;21(8). doi: 10.1093/femsyr/foab066.

Abstract

Rhodotorula toruloides has been increasingly explored as a host for bioproduction of lipids, fatty acid derivatives and terpenoids. Various genetic tools have been developed, but neither a centromere nor an autonomously replicating sequence (ARS), both necessary elements for stable episomal plasmid maintenance, has yet been reported. In this study, cleavage under targets and release using nuclease (CUT&RUN), a method used for genome-wide mapping of DNA-protein interactions, was used to identify R. toruloides IFO0880 genomic regions associated with the centromeric histone H3 protein Cse4, a marker of centromeric DNA. Fifteen putative centromeres ranging from 8 to 19 kb in length were identified and analyzed, and four were tested for, but did not show, ARS activity. These centromeric sequences contained below average GC content, corresponded to transcriptional cold spots, were primarily nonrepetitive and shared some vestigial transposon-related sequences but otherwise did not show significant sequence conservation. Future efforts to identify an ARS in this yeast can utilize these centromeric DNA sequences to improve the stability of episomal plasmids derived from putative ARS elements.

摘要

罗氏酵母已被越来越多地探索作为生物生产脂质、脂肪酸衍生物和萜类化合物的宿主。已经开发了各种遗传工具,但尚未报道稳定的附加体质粒维持所必需的着丝粒和自主复制序列(ARS)。在这项研究中,使用切割目标物和释放使用核酸酶(CUT&RUN)的方法,用于全基因组 DNA-蛋白质相互作用图谱绘制的方法,鉴定了与着丝粒组蛋白 H3 蛋白 Cse4 相关的罗氏酵母 IFO0880 基因组区域,Cse4 是着丝粒 DNA 的标志物。鉴定并分析了 15 个长度在 8 到 19kb 之间的假定着丝粒,其中 4 个测试了但未显示 ARS 活性。这些着丝粒序列的 GC 含量低于平均值,对应于转录冷点,主要是非重复的,并共享一些残余转座子相关序列,但其他方面没有显示出显著的序列保守性。未来在这种酵母中鉴定 ARS 的工作可以利用这些着丝粒 DNA 序列来提高源自假定 ARS 元件的附加体质粒的稳定性。

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