Histone deacetylase Hos2 regulates protein expression noise by potentially modulating the protein translation machinery

Author:

Lin Wei-Han12,Opoc Florica J G2,Liao Chia-Wei2,Roy Kevin R34,Steinmetz Lars M345,Leu Jun-Yi12ORCID

Affiliation:

1. Doctoral Program in Microbial Genomics, National Chung Hsing University and Academia Sinica , Taiwan

2. Institute of Molecular Biology, Academia Sinica , Taipei 115 , Taiwan

3. Stanford Genome Technology Center, Stanford University , Palo Alto , CA 94304 , USA

4. Department of Genetics, Stanford University School of Medicine , Stanford , CA 94305 , USA

5. European Molecular Biology Laboratory (EMBL), Genome Biology Unit , Heidelberg 69117 , Germany

Abstract

Abstract 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.

Funder

National Institutes of Health

Academia Sinica of Taiwan

National Science and Technology Council

Publisher

Oxford University Press (OUP)

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