Histone deacetylase Hos2 regulates protein expression noise by potentially modulating the protein translation machinery.
Wei-Han LinFlorica J G OpocChia-Wei LiaoKevin R RoyLars M SteinmetzJun-Yi LeuPublished in: Nucleic acids research (2024)
Non-genetic variations derived from expression noise at transcript or protein levels can result in cell-to-cell heterogeneity within an isogenic population. Although cells have developed strategies to reduce noise in some cellular functions, this heterogeneity can also facilitate varying levels of regulation and provide evolutionary benefits in specific environments. Despite several general characteristics of cellular noise having been revealed, the detailed molecular pathways underlying noise regulation remain elusive. Here, we established a dual-fluorescent reporter system in Saccharomyces cerevisiae and performed experimental evolution to search for mutations that increase expression noise. By analyzing evolved cells using bulk segregant analysis coupled with whole-genome sequencing, we identified the histone deacetylase Hos2 as a negative noise regulator. A hos2 mutant down-regulated multiple ribosomal protein genes and exhibited partially compromised protein translation, indicating that Hos2 may regulate protein expression noise by modulating the translation machinery. Treating cells with translation inhibitors or introducing mutations into several Hos2-regulated ribosomal protein genes-RPS9A, RPS28B and RPL42A-enhanced protein expression noise. Our study provides an effective strategy for identifying noise regulators and also sheds light on how cells regulate non-genetic variation through protein translation.
Keyphrases
- air pollution
- induced apoptosis
- histone deacetylase
- single cell
- cell cycle arrest
- binding protein
- protein protein
- genome wide
- transcription factor
- amino acid
- saccharomyces cerevisiae
- signaling pathway
- poor prognosis
- endoplasmic reticulum stress
- rna seq
- small molecule
- stem cells
- crispr cas
- gene expression
- cell therapy
- oxidative stress
- copy number
- mesenchymal stem cells
- genome wide identification