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Fdo1, Fkh1, Fkh2, and the Swi6-Mbp1 MBF complex regulate Mcd1 levels to impact eco1 rad61 cell growth in Saccharomyces cerevisiae.
- Source :
-
Genetics [Genetics] 2024 Oct 07; Vol. 228 (2). - Publication Year :
- 2024
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Abstract
- Cohesins promote proper chromosome segregation, gene transcription, genomic architecture, DNA condensation, and DNA damage repair. Mutations in either cohesin subunits or regulatory genes can give rise to severe developmental abnormalities (such as Robert Syndrome and Cornelia de Lange Syndrome) and also are highly correlated with cancer. Despite this, little is known about cohesin regulation. Eco1 (ESCO2/EFO2 in humans) and Rad61 (WAPL in humans) represent two such regulators but perform opposing roles. Eco1 acetylation of cohesin during S phase, for instance, stabilizes cohesin-DNA binding to promote sister chromatid cohesion. On the other hand, Rad61 promotes the dissociation of cohesin from DNA. While Eco1 is essential, ECO1 and RAD61 co-deletion results in yeast cell viability, but only within a limited temperature range. Here, we report that eco1rad61 cell lethality is due to reduced levels of the cohesin subunit Mcd1. Results from a suppressor screen further reveals that FDO1 deletion rescues the temperature-sensitive (ts) growth defects exhibited by eco1rad61 double mutant cells by increasing Mcd1 levels. Regulation of MCD1 expression, however, appears more complex. Elevated expression of MBP1, which encodes a subunit of the MBF transcription complex, also rescues eco1rad61 cell growth defects. Elevated expression of SWI6, however, which encodes the Mbp1-binding partner of MBF, exacerbates eco1rad61 cell growth and also abrogates the Mpb1-dependent rescue. Finally, we identify two additional transcription factors, Fkh1 and Fkh2, that impact MCD1 expression. In combination, these findings provide new insights into the nuanced and multi-faceted transcriptional pathways that impact MCD1 expression.<br />Competing Interests: Conflicts of interest The author(s) declare no conflict of interest.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of The Genetics Society of America.)
- Subjects :
- Acetyltransferases genetics
Acetyltransferases metabolism
Cohesins
DNA-Binding Proteins genetics
DNA-Binding Proteins metabolism
Nuclear Proteins genetics
Nuclear Proteins metabolism
Transcription Factors genetics
Transcription Factors metabolism
Gene Expression Regulation, Fungal
Forkhead Transcription Factors
Saccharomyces cerevisiae Proteins genetics
Saccharomyces cerevisiae Proteins metabolism
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae growth & development
Chromosomal Proteins, Non-Histone metabolism
Chromosomal Proteins, Non-Histone genetics
Cell Cycle Proteins metabolism
Cell Cycle Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1943-2631
- Volume :
- 228
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 39110836
- Full Text :
- https://doi.org/10.1093/genetics/iyae128