Critical importance of DNA binding for CSL protein functions in fission yeast.
Anna MarešováMartina OravcováMaría Rodríguez-LópezMiluše HradilováViacheslav ZemlianskiRobert HäslerPablo HernándezJürg BählerMartin PřevorovskýPublished in: Journal of cell science (2024)
CSL (CBF1/RBP-Jκ/Suppressor of Hairless/LAG-1) proteins are conserved transcription factors found in animals and fungi. In fission yeast, they regulate various cellular processes, including cell cycle progression, lipid metabolism, and cell adhesion. CSL proteins bind to DNA through their N-terminal Rel-like domain and central beta-trefoil domain. Here, we investigated the importance of DNA binding for CSL functions in the fission yeast Schizosaccharomyces pombe. We created CSL mutants with disrupted DNA binding and found that the vast majority of CSL functions depend on intact DNA binding. Specifically, DNA binding is crucial for the regulation of cell adhesion, lipid metabolism, cell cycle progression, long non-coding RNA expression, and genome integrity maintenance. Interestingly, perturbed lipid metabolism leads to chromatin structure changes, potentially linking lipid metabolism to the diverse CSL-associated phenotypes. Our study highlights the critical role of DNA binding for CSL protein functions in fission yeast.
Keyphrases
- dna binding
- transcription factor
- cell cycle
- cell adhesion
- long non coding rna
- poor prognosis
- cell proliferation
- saccharomyces cerevisiae
- fatty acid
- binding protein
- gene expression
- cell wall
- amino acid
- protein protein
- single molecule
- circulating tumor
- dna damage
- small molecule
- high resolution
- oxidative stress
- atomic force microscopy