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.Základní údaje
Originální název
Overlapping and separable activities of BRA-2 and HIM-17 promote occurrence and regulation of pairing and synapsis during Caenorhabditis elegans meiosis
Autoři
BLAŽÍČKOVÁ, Jitka; Shalini TRIVEDI; Richard BOWMAN; Sowmya Sivakumar GEETHA; Silma SUBAH; Michelle SCUZZARELLA; Alexander CHANG; Uma R CHANDRAN; Judith L YANOWITZ; Sarit SMOLIKOVE; Verena JANTSCH; Monique ZETKA a Nicola SILVA
Vydání
Nature Communications, Berlin, Nature Research, 2025, 2041-1723
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Německo
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 15.700 v roce 2024
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/25:00140941
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
BRA-2; HIM-17; meiosis; pairing; synapsis
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 16. 3. 2026 07:59, Mgr. Tereza Miškechová
Anotace
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.
Návaznosti
| GA23-04918S, projekt VaV |
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| 90242, velká výzkumná infrastruktura |
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| 90250, velká výzkumná infrastruktura |
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| 90254, velká výzkumná infrastruktura |
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