Suppr超能文献

在铜绿假单胞菌染色体分离中 ,SMC 和 MksBEF 的交替动力学。

Alternating Dynamics of , SMC, and MksBEF in Segregation of Pseudomonas aeruginosa Chromosome.

机构信息

Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, USA.

Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, USA

出版信息

mSphere. 2020 Sep 9;5(5):e00238-20. doi: 10.1128/mSphere.00238-20.

Abstract

Condensins are essential for global chromosome organization in diverse bacteria. Atypically, the chromosome encodes condensins from two superfamilies, SMC-ScpAB and MksBEF. Here, we report that the two proteins play specialized roles in chromosome packing and segregation and are synthetically lethal with ParB. Inactivation of SMC or MksB affected, in a protein-dependent manner, global chromosome layout and its timing of segregation and sometimes triggered a chromosomal inversion. The localization pattern was also unique to each protein. SMC clusters colocalized with throughout the cell cycle except shortly after origin duplication, whereas MksB clusters emerged at cell quarters shortly prior to duplication and stayed there even after cell division. The relocation of the proteins was abrupt and coordinated with dynamic. These data reveal that the two condensins play distinct dual roles in chromosome maintenance by organizing it and mediating its segregation. Furthermore, the choreography of condensins and relocations suggest an elegant mechanism for the birth and maturation of chromosomes. Mechanisms that define the chromosome as a structural entity remain unknown. Key elements in this process are condensins, which globally organize chromosomes and contribute to their segregation. This study characterized condensin and chromosome dynamics in , which harbors condensins from two major protein superfamilies, SMC and MksBEF. The study revealed that both proteins play a dual role in chromosome maintenance by spatially organizing the chromosomes and guiding their segregation but can substitute for each other in some activities. The timing of chromosome, SMC, and MksBEF relocation was highly ordered and interdependent, revealing causative relationships in the process. Moreover, MksBEF produced clusters at the site of chromosome replication that survived cell division and remained in place until replication was complete. Overall, these data delineate the functions of condensins from the SMC and MksBEF superfamilies, reveal the existence of a chromosome organizing center, and suggest a mechanism that might explain the biogenesis of chromosomes.

摘要

凝聚素对于不同细菌的全局染色体组织至关重要。通常情况下,染色体编码来自两个超家族的凝聚素,SMC-ScpAB 和 MksBEF。在这里,我们报告这两种蛋白质在染色体包装和分离中发挥专门作用,并且与 ParB 具有合成致死性。SMC 或 MksB 的失活以依赖于蛋白质的方式影响全局染色体布局及其分离的时间,有时会触发染色体倒位。定位模式也对每种蛋白质都是独特的。SMC 簇在整个细胞周期中与 共定位,除了在原点复制后不久,而 MksB 簇在细胞四分之一处出现,在细胞分裂后仍留在那里。蛋白质的重定位是突然的,并且与 动态协调。这些数据表明,两种凝聚素通过组织染色体并介导其分离,在染色体维持中发挥独特的双重作用。此外,凝聚素和 重定位的协调提示了染色体诞生和成熟的优雅机制。定义染色体为结构实体的机制仍然未知。该过程中的关键要素是凝聚素,它全局组织染色体并有助于其分离。本研究在 中表征了凝聚素和染色体动力学,该 含有来自两个主要蛋白质超家族 SMC 和 MksBEF 的凝聚素。研究表明,两种蛋白质通过空间组织染色体并指导其分离在染色体维持中发挥双重作用,但在某些活动中可以相互替代。染色体、SMC 和 MksBEF 重定位的时间高度有序且相互依赖,揭示了该过程中的因果关系。此外,MksBEF 在染色体复制部位产生的簇在细胞分裂后仍然存在,并保持原位,直到复制完成。总的来说,这些数据描绘了 SMC 和 MksBEF 超家族凝聚素的功能,揭示了染色体组织中心的存在,并提出了一种可能解释染色体发生的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7050/7485682/d2332de686ac/mSphere.00238-20-f0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验