Detailed Information on Publication Record
2022
Continuous double-strand break induction and their differential processing sustain chiasma formation during Caenorhabditis elegans meiosis
HICKS, Tara, Shalini TRIVEDI, Mikayla EPPERT, Richard BOWMAN, Hui TIAN et. al.Basic information
Original name
Continuous double-strand break induction and their differential processing sustain chiasma formation during Caenorhabditis elegans meiosis
Authors
HICKS, Tara, Shalini TRIVEDI (356 India, belonging to the institution), Mikayla EPPERT, Richard BOWMAN, Hui TIAN, Amna DAFALLA, Caroline CRAHAN, Sarit SMOLIKOVE and Nicola SILVA (380 Italy, guarantor, belonging to the institution)
Edition
Cell Reports, CAMBRIDGE, Cell Press, 2022, 2211-1247
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 8.800
RIV identification code
RIV/00216224:14110/22:00128181
Organization unit
Faculty of Medicine
UT WoS
000869019800008
Keywords in English
Caenorhabditis elegans meiosis; double-strand break induction; sustain chiasma formation
Tags
International impact, Reviewed
Změněno: 20/1/2023 14:10, Mgr. Tereza Miškechová
Abstract
V originále
Faithful chromosome segregation into gametes depends on Spo11-induced DNA double-strand breaks (DSBs). These yield single-stranded 30 tails upon resection to promote crossovers (COs). While early Mre11-dependent end resection is the predominant pathway in most organisms, Exo1 or Dna2/BLM can also contribute to the efficient processing of meiotic DSBs. Although its enzymatic activity has been thor-oughly dissected, the temporal dynamics underlying Spo11 activity have remained mostly elusive. We show that, in Caenorhabditis elegans, SPO-11-mediated DSB induction takes place throughout early meiotic prophase I until mid-late pachynema. We find that late DSBs are essential for CO formation and are prefer-entially processed by EXO-1 and DNA-2 in a redundant fashion. Further, EXO-1-DNA-2-mediated resection ensures completion of conservative DSB repair and discourages activation of KU-dependent end joining. Taken together, our data unveil important temporal aspects of DSB induction and identify previously un-known functional implications for EXO-1-DNA-2-mediated resection activity in C. elegans.
Links
GA20-08819S, research and development project |
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LM2018129, research and development project |
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