2025
Overlapping and separable activities of BRA-2 and HIM-17 promote occurrence and regulation of pairing and synapsis during Caenorhabditis elegans meiosis
BLAŽÍČKOVÁ, Jitka; Shalini TRIVEDI; Richard BOWMAN; Sowmya Sivakumar GEETHA; Silma SUBAH et. al.Basic information
Original name
Overlapping and separable activities of BRA-2 and HIM-17 promote occurrence and regulation of pairing and synapsis during Caenorhabditis elegans meiosis
Authors
BLAŽÍČKOVÁ, Jitka (203 Czech Republic, belonging to the institution); Shalini TRIVEDI (356 India, belonging to the institution); Richard BOWMAN; Sowmya Sivakumar GEETHA; Silma SUBAH; Michelle SCUZZARELLA; Alexander CHANG; Uma R CHANDRAN; Judith L YANOWITZ; Sarit SMOLIKOVE; Verena JANTSCH; Monique ZETKA and Nicola SILVA (380 Italy, belonging to the institution)
Edition
Nature Communications, Berlin, Nature Research, 2025, 2041-1723
Other information
Language
English
Type of outcome
Article in a journal
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Germany
Confidentiality degree
is not subject to a state or trade secret
References:
Impact factor
Impact factor: 14.700 in 2023
Organization unit
Faculty of Medicine
UT WoS
001445062800033
EID Scopus
2-s2.0-105000115678
Keywords in English
BRA-2; HIM-17; meiosis; pairing; synapsis
Tags
International impact, Reviewed
Changed: 2/4/2025 10:48, Mgr. Tereza Miškechová
Abstract
V originále
Faithful meiotic segregation requires pairwise alignment of the homologous chromosomes and their synaptonemal complex (SC) mediated stabilization. Here, we investigate factors that promote and coordinate these events during C. elegans meiosis. We identify BRA-2 (BMP Receptor Associated family member 2) as an interactor of HIM-17, previously shown to promote double-strand break formation. We found that loss of bra-2 impairs synapsis elongation without affecting homolog recognition, chromosome movement or SC maintenance. Epistasis analyses reveal previously unrecognized activities for HIM-17 in regulating homolog pairing and SC assembly in a partially overlapping manner with BRA-2. We show that removing bra-2 or him-17 restores nuclear clustering, recruitment of PLK-2 at the nuclear periphery, and abrogation of ectopic synapsis in htp-1 mutants, suggesting intact CHK-2-mediated signaling and presence of a barrier that prevents SC polymerization in the absence of homology. Our findings shed light on the regulatory mechanisms ensuring faithful pairing and synapsis.
Links
GA23-04918S, research and development project |
| ||
LM2023042, research and development project |
| ||
LM2023050, research and development project |
| ||
90254, large research infrastructures |
|