Detailed Information on Publication Record
2022
Meiotic exit in Arabidopsis is driven by P-body-mediated inhibition of translation
CAIRO CALZADA, Albert, Anna VARGOVÁ, Neha SHUKLA, Claudio CAPITAO, Pavlína MIKULKOVÁ et. al.Basic information
Original name
Meiotic exit in Arabidopsis is driven by P-body-mediated inhibition of translation
Authors
CAIRO CALZADA, Albert (724 Spain, belonging to the institution), Anna VARGOVÁ (703 Slovakia, belonging to the institution), Neha SHUKLA (356 India, belonging to the institution), Claudio CAPITAO, Pavlína MIKULKOVÁ (203 Czech Republic, belonging to the institution), Soňa VALUCHOVÁ (703 Slovakia, belonging to the institution), Jana PEČINKOVÁ (203 Czech Republic, belonging to the institution), Petra BULANKOVA and Karel ŘÍHA (203 Czech Republic, guarantor, belonging to the institution)
Edition
Science, WASHINGTON, AMER ASSOC ADVANCEMENT SCIENCE, 2022, 0036-8075
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 56.900
RIV identification code
RIV/00216224:14740/22:00127511
Organization unit
Central European Institute of Technology
UT WoS
000837874700039
Keywords in English
MESSENGER-RNA DECAY; SMG7; PROGRAM; PROTEIN; MEIOSIS; REVEALS;BODIES
Tags
International impact, Reviewed
Změněno: 8/10/2024 10:31, Ing. Martina Blahová
Abstract
V originále
Meiosis, at the transition between diploid and haploid life cycle phases, is accompanied by reprograming of cell division machinery and followed by a transition back to mitosis. We show that, in Arabidopsis, this transition is driven by inhibition of translation, achieved by a mechanism that involves processing bodies (P-bodies). During the second meiotic division, the meiosis-specific protein THREE-DIVISION MUTANT 1 (TDM1) is incorporated into P-bodies through interaction with SUPPRESSOR WITH MORPHOGENETIC EFFECTS ON GENITALIA 7 (SMG7). TDM1 attracts eIF4F, the main translation initiation complex, temporarily sequestering it in P-bodies and inhibiting translation. The failure of tdm1 mutants to terminate meiosis can be overcome by chemical inhibition of translation. We propose that TDM1-containing P-bodies down-regulate expression of meiotic transcripts to facilitate transition of cell fates to postmeiotic gametophyte differentiation.
Links
EF15_003/0000479, research and development project |
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90129, large research infrastructures |
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