AI Article Synopsis

  • Non-genetic variations in gene expression can lead to differences between cells in the same population, known as cell-to-cell heterogeneity.
  • While cells typically work to minimize this variability, it can sometimes offer advantages in certain environments, though the specific molecular pathways controlling this "noise" are not fully understood.
  • In a study using yeast, researchers discovered that the histone deacetylase Hos2 acts as a negative regulator of expression noise, influencing protein translation by down-regulating certain ribosomal protein genes, demonstrating new insights into how cells manage non-genetic variations.

Article 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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11260488PMC
http://dx.doi.org/10.1093/nar/gkae432DOI Listing

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