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枯草芽孢杆菌的染色体分离高度不均一。

Chromosome segregation in B. subtilis is highly heterogeneous.

机构信息

LOEWE Center for Synthetic Microbiology, SYNMIKRO, Philipps Universität Marburg, Marburg, Germany.

Department of Chemistry, Philipps Universität Marburg, Marburg, Germany.

出版信息

BMC Res Notes. 2020 Oct 9;13(1):477. doi: 10.1186/s13104-020-05322-9.

Abstract

OBJECTIVE

The bacterial cell cycle comprises initiation of replication and ensuing elongation, concomitant chromosome segregation (in some organisms with a delay termed cohesion), and finally cell division. By quantifying the number of origin and terminus regions in exponentially growing Bacillus subtilis cells, and after induction of DNA damage, we aimed at determining cell cycle parameters at different growth rates at a single cell level.

RESULTS

B. subtilis cells are mostly mero-oligoploid during fast growth and diploid during slow growth. However, we found that the number of replication origins and of termini is highly heterogeneous within the cell population at two different growth rates, and that even at slow growth, a majority of cells attempts to maintain more than a single chromosome at all times of the cell cycle. Heterogeneity of chromosome copy numbers may reflect different subpopulations having diverging growth rates even during exponential growth conditions. Cells continued to initiate replication and segregate chromosomes after induction of DNA damage, as judged by an increase in origin numbers per cell, showing that replication and segregation are relatively robust against cell cycle perturbation.

摘要

目的

细菌细胞周期包括复制的起始和随后的延伸,伴随着染色体的分离(在某些生物体中,这种分离伴随着延迟,称为黏连),最后是细胞分裂。通过定量测定指数生长期枯草芽孢杆菌细胞中的起始和终止区域的数量,并在诱导 DNA 损伤后,我们旨在确定在单个细胞水平上不同生长速率下的细胞周期参数。

结果

在快速生长时,枯草芽孢杆菌细胞主要是单倍体或寡倍体,而在缓慢生长时则是二倍体。然而,我们发现,在两个不同的生长速率下,细胞群体中的复制起始点和终止点的数量存在高度异质性,即使在缓慢生长时,大多数细胞在细胞周期的任何时候都试图维持不止一条染色体。染色体拷贝数的异质性可能反映了不同的亚群即使在指数生长条件下也有不同的生长速率。通过细胞中起始点数量的增加来判断,细胞在诱导 DNA 损伤后继续进行复制和染色体分离,这表明复制和分离对细胞周期扰动具有相对的稳健性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cfd/7547420/680285633a2e/13104_2020_5322_Fig1_HTML.jpg

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