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本文引用的文献

1
The Synchronization of Replication and Division Cycles in Individual E. coli Cells.单个大肠杆菌细胞中复制与分裂周期的同步
Cell. 2016 Jul 28;166(3):729-739. doi: 10.1016/j.cell.2016.06.052.
2
Structure-function analysis of the extracellular domain of the pneumococcal cell division site positioning protein MapZ.肺炎链球菌细胞分裂定位蛋白 MapZ 胞外结构域的结构-功能分析。
Nat Commun. 2016 Jun 27;7:12071. doi: 10.1038/ncomms12071.
3
Rewiring the Pneumococcal Cell Cycle with Serine/Threonine- and Tyrosine-kinases.用丝氨酸/苏氨酸激酶和酪氨酸激酶重塑肺炎球菌细胞周期。
Trends Microbiol. 2016 Sep;24(9):713-724. doi: 10.1016/j.tim.2016.04.004. Epub 2016 Apr 26.
4
Connecting the dots of the bacterial cell cycle: Coordinating chromosome replication and segregation with cell division.连接细菌细胞周期的点:协调染色体复制和分离与细胞分裂。
Semin Cell Dev Biol. 2016 May;53:2-9. doi: 10.1016/j.semcdb.2015.11.012. Epub 2015 Dec 17.
5
Oufti: an integrated software package for high-accuracy, high-throughput quantitative microscopy analysis.Oufti:一款用于高精度、高通量定量显微镜分析的集成软件包。
Mol Microbiol. 2016 Feb;99(4):767-77. doi: 10.1111/mmi.13264. Epub 2015 Dec 18.
6
Regulation of contractile ring formation and septation in Schizosaccharomyces pombe.粟酒裂殖酵母中收缩环形成与隔膜形成的调控
Curr Opin Microbiol. 2015 Dec;28:46-52. doi: 10.1016/j.mib.2015.08.001. Epub 2015 Sep 3.
7
Minimal Peptidoglycan (PG) Turnover in Wild-Type and PG Hydrolase and Cell Division Mutants of Streptococcus pneumoniae D39 Growing Planktonically and in Host-Relevant Biofilms.肺炎链球菌D39野生型、肽聚糖(PG)水解酶及细胞分裂突变体在浮游生长及与宿主相关生物膜中生长时的最小肽聚糖(PG)周转
J Bacteriol. 2015 Nov;197(21):3472-85. doi: 10.1128/JB.00541-15. Epub 2015 Aug 24.
8
Condensin- and Replication-Mediated Bacterial Chromosome Folding and Origin Condensation Revealed by Hi-C and Super-resolution Imaging.Hi-C 和超高分辨率成像揭示了凝聚素和复制介导的细菌染色体折叠和复制起点浓缩。
Mol Cell. 2015 Aug 20;59(4):588-602. doi: 10.1016/j.molcel.2015.07.020.
9
Chromosome replication, cell growth, division and shape: a personal perspective.染色体复制、细胞生长、分裂与形态:个人观点
Front Microbiol. 2015 Aug 3;6:756. doi: 10.3389/fmicb.2015.00756. eCollection 2015.
10
Red Fluorescent Proteins for Gene Expression and Protein Localization Studies in Streptococcus pneumoniae and Efficient Transformation with DNA Assembled via the Gibson Assembly Method.用于肺炎链球菌基因表达和蛋白质定位研究的红色荧光蛋白以及通过吉布森组装法组装的DNA的高效转化
Appl Environ Microbiol. 2015 Oct;81(20):7244-52. doi: 10.1128/AEM.02033-15. Epub 2015 Aug 7.

染色体分离驱动. 中的分裂位点选择。

Chromosome segregation drives division site selection in .

机构信息

Molecular Genetics Group, Groningen Biomolecular Sciences and Biotechnology Institute, Centre for Synthetic Biology, University of Groningen, 9747 AG Groningen, The Netherlands.

Department of Fundamental Microbiology, Faculty of Biology and Medicine, University of Lausanne, CH-1015 Lausanne, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 2017 Jul 18;114(29):E5959-E5968. doi: 10.1073/pnas.1620608114. Epub 2017 Jul 3.

DOI:10.1073/pnas.1620608114
PMID:28674002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5530652/
Abstract

Accurate spatial and temporal positioning of the tubulin-like protein FtsZ is key for proper bacterial cell division. (pneumococcus) is an oval-shaped, symmetrically dividing opportunistic human pathogen lacking the canonical systems for division site control (nucleoid occlusion and the Min-system). Recently, the early division protein MapZ was identified and implicated in pneumococcal division site selection. We show that MapZ is important for proper division plane selection; thus, the question remains as to what drives pneumococcal division site selection. By mapping the cell cycle in detail, we show that directly after replication both chromosomal origin regions localize to the future cell division sites, before FtsZ. Interestingly, Z-ring formation occurs coincidently with initiation of DNA replication. Perturbing the longitudinal chromosomal organization by mutating the condensin SMC, by CRISPR/Cas9-mediated chromosome cutting, or by poisoning DNA decatenation resulted in mistiming of MapZ and FtsZ positioning and subsequent cell elongation. Together, we demonstrate an intimate relationship between DNA replication, chromosome segregation, and division site selection in the pneumococcus, providing a simple way to ensure equally sized daughter cells.

摘要

准确的微管样蛋白 FtsZ 的时空定位对于细菌细胞的正确分裂至关重要。肺炎链球菌是一种椭圆形、对称分裂的机会主义人类病原体,缺乏典型的分裂位点控制(核区阻断和 Min 系统)系统。最近,早期分裂蛋白 MapZ 被鉴定出来,并与肺炎链球菌的分裂位点选择有关。我们表明 MapZ 对正确的分裂平面选择很重要;因此,问题仍然是肺炎链球菌的分裂位点选择是由什么驱动的。通过详细绘制细胞周期图,我们表明,在 FtsZ 之前,直接在复制之后,染色体起始区域就定位到未来的细胞分裂位点。有趣的是,Z 环的形成与 DNA 复制的起始同时发生。通过突变凝聚素 SMC、CRISPR/Cas9 介导的染色体切割或毒害 DNA 解连环来破坏纵向染色体组织,导致 MapZ 和 FtsZ 定位和随后的细胞伸长时机错误。总之,我们证明了肺炎链球菌中 DNA 复制、染色体分离和分裂位点选择之间的密切关系,为确保均等大小的子细胞提供了一种简单的方法。