Genetic battle between Helicobacter pylori and humans. The mechanism underlying homologous recombination in bacteria, which can infect human cells

2014 ◽  
Vol 16 (10) ◽  
pp. 833-839 ◽  
Author(s):  
Katsuhiro Hanada ◽  
Yoshio Yamaoka
Genetics ◽  
2004 ◽  
Vol 166 (4) ◽  
pp. 1641-1649
Author(s):  
Laura Maringele ◽  
David Lydall

Abstract Telomerase-defective budding yeast cells escape senescence by using homologous recombination to amplify telomeric or subtelomeric structures. Similarly, human cells that enter senescence can use homologous recombination for telomere maintenance, when telomerase cannot be activated. Although recombination proteins required to generate telomerase-independent survivors have been intensively studied, little is known about the nucleases that generate the substrates for recombination. Here we demonstrate that the Exo1 exonuclease is an initiator of the recombination process that allows cells to escape senescence and become immortal in the absence of telomerase. We show that EXO1 is important for generating type I survivors in yku70Δ mre11Δ cells and type II survivors in tlc1Δ cells. Moreover, in tlc1Δ cells, EXO1 seems to contribute to the senescence process itself.


DNA Repair ◽  
2008 ◽  
Vol 7 (10) ◽  
pp. 1624-1635 ◽  
Author(s):  
B WALDMAN ◽  
Y WANG ◽  
K KILARU ◽  
Z YANG ◽  
A BHASIN ◽  
...  

2012 ◽  
Vol 55 (7) ◽  
pp. 3011-3020 ◽  
Author(s):  
Fei Huang ◽  
Olga M. Mazina ◽  
Isaac J. Zentner ◽  
Simon Cocklin ◽  
Alexander V. Mazin

2020 ◽  
Vol 219 (10) ◽  
Author(s):  
David G. Maranon ◽  
Neelam Sharma ◽  
Yuxin Huang ◽  
Platon Selemenakis ◽  
Meiling Wang ◽  
...  

NUCKS1 (nuclear ubiquitous casein kinase and cyclin-dependent kinase substrate 1) is a chromatin-associated, vertebrate-specific, and multifunctional protein with a role in DNA damage signaling and repair. Previously, we have shown that NUCKS1 helps maintain homologous recombination (HR) DNA repair in human cells and functions as a tumor suppressor in mice. However, the mechanisms by which NUCKS1 positively impacts these processes had remained unclear. Here, we show that NUCKS1 physically and functionally interacts with the DNA motor protein RAD54. Upon exposure of human cells to DNA-damaging agents, NUCKS1 controls the resolution of RAD54 foci. In unperturbed cells, NUCKS1 prevents RAD54’s inappropriate engagement with RAD51AP1. In vitro, NUCKS1 stimulates the ATPase activity of RAD54 and the RAD51–RAD54-mediated strand invasion step during displacement loop formation. Taken together, our data demonstrate that the NUCKS1 protein is an important new regulator of the spatiotemporal events in HR.


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