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在放线菌谷氨酸棒杆菌中,由一个保守的凝聚蛋白-ParB 系统进行染色体组织。

Chromosome organization by a conserved condensin-ParB system in the actinobacterium Corynebacterium glutamicum.

机构信息

Ludwig-Maximilians-Universität München, Fakultät Biologie, 82152, Planegg-Martinsried, Germany.

Christian-Albrechts-Universität zu Kiel, Institut für allgemeine Mikrobiologie, 24118, Kiel, Germany.

出版信息

Nat Commun. 2020 Mar 20;11(1):1485. doi: 10.1038/s41467-020-15238-4.

Abstract

Higher-order chromosome folding and segregation are tightly regulated in all domains of life. In bacteria, details on nucleoid organization regulatory mechanisms and function remain poorly characterized, especially in non-model species. Here, we investigate the role of DNA-partitioning protein ParB and SMC condensin complexes in the actinobacterium Corynebacterium glutamicum. Chromosome conformation capture reveals SMC-mediated long-range interactions around ten centromere-like parS sites clustered at the replication origin (oriC). At least one oriC-proximal parS site is necessary for reliable chromosome segregation. We use chromatin immunoprecipitation and photoactivated single-molecule localization microscopy to show the formation of distinct, parS-dependent ParB-nucleoprotein subclusters. We further show that SMC/ScpAB complexes, loaded via ParB at parS sites, mediate chromosomal inter-arm contacts (as previously shown in Bacillus subtilis). However, the MukBEF-like SMC complex MksBEFG does not contribute to chromosomal DNA-folding; instead, this complex is involved in plasmid maintenance and interacts with the polar oriC-tethering factor DivIVA. Our results complement current models of ParB-SMC/ScpAB crosstalk and show that some condensin complexes evolved functions that are apparently uncoupled from chromosome folding.

摘要

高等染色体折叠和分离在所有生命领域都受到严格调控。在细菌中,关于核区组织调节机制和功能的细节仍知之甚少,特别是在非模式物种中。在这里,我们研究了 DNA 分区蛋白 ParB 和 SMC 凝聚酶复合物在放线菌谷氨酸棒杆菌中的作用。染色体构象捕获显示 SMC 介导的十个类似于着丝粒的 parS 位点在复制原点(oriC)周围的长程相互作用。至少有一个 oriC 近端 parS 位点对于可靠的染色体分离是必要的。我们使用染色质免疫沉淀和光活化单分子定位显微镜显示了形成独特的、依赖于 parS 的 ParB-核蛋白亚群集。我们进一步表明,SMC/ScpAB 复合物通过 ParB 在 parS 位点加载,介导染色体间臂接触(如先前在枯草芽孢杆菌中所示)。然而,MukBEF 样 SMC 复合物 MksBEFG 不参与染色体 DNA 折叠;相反,该复合物参与质粒维持,并与极性 oriC 系绳因子 DivIVA 相互作用。我们的结果补充了 ParB-SMC/ScpAB 串扰的现有模型,并表明一些凝聚酶复合物的进化功能显然与染色体折叠无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e747/7083940/45cbbcd9b2f2/41467_2020_15238_Fig1_HTML.jpg

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