Badrinarayanan, A. | Search bioRxiv

bioRxiv2020

Asymmetric chromosome segregation and cell division in DNA damage-induced bacterial filaments

Faithful propagation of life requires coordination of DNA replication and segregation with cell growth and division. In bacteria, this results in cell size homeostasis and periodicity in replication and division. The situation is perturbed under stress such as DNA damage, which induces filamentation as cell cycle progression is blocked to allow for repair. Mechanisms that release this morphological state for re-entry into wild type growth are unclear. Here we show that damage recovery is mediated via asymmetric division of Escherichia coli filaments, producing short daughter cells with wild type size and growth dynamics. Division restoration at this polar site is governed by coordinated action of divisome positioning by the Min system and modulation of division licensing by the terminus region of the chromosome, with MatP playing a central role in this process. Collectively, our study highlights a key role for concurrency between chromosome (and specifically terminus) segregation and cell division in daughter cell size maintenance during filamentous divisions and suggests a central function for asymmetric division in mediating cellular recovery from a stressed state.

microbiology↗

bioRxiv2019

Evolutionary analysis of bacterial Non-Homologous End Joining Repair

DNA double-strand breaks (DSBs) are a threat to genome stability. In all domains of life, DSBs are faithfully fixed via homologous recombination. Recombination requires the presence of an uncut copy of duplex DNA that is used as a template for repair. Alternatively, in the absence of a template, cells utilize error-prone Non-homologous end joining (NHEJ). Although ubiquitously found in eukaryotes, NHEJ is not universally present in bacteria. It is unclear as to why many prokaryotes lack this pathway. To understand what could have led to the current distribution of bacterial NHEJ, we carried out comparative genomics and phylogenetic analysis across ~6000 genomes. Our results show that this pathway is sporadically distributed across the phylogeny. Ancestral reconstruction further suggests that NHEJ was absent in the eubacterial ancestor, and can be acquired via specific routes. Integrating NHEJ occurrence data for archaea, we also find evidence for extensive horizontal exchange of NHEJ genes between the two kingdoms as well as across bacterial clades. The pattern of occurrence in bacteria is consistent with correlated evolution of NHEJ with key genome characteristics of genome size and growth rates; NHEJ presence is associated with large genome sizes and/or slow growth rates, with the former being the dominant correlate. Given the central role these traits play in determining the ability to carry out recombination, it is possible that the evolutionary history of bacterial NHEJ may have been shaped by requirement for efficient DSB repair.

bioinformatics↗