Independent evolution of transcript abundance and gene regulatory dynamics

Gat Krieger, Offir Lupo, Avraham A. Levy, Naama Barkai*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Changes in gene expression drive novel phenotypes, raising interest in how gene expression evolves. In contrast to the static genome, cells modulate gene expression in response to changing environments. Previous comparative studies focused on specific conditions, describing interspecies variation in expression levels, but providing limited information about variation across different conditions. To close this gap, we profiled mRNA levels of two related yeast species in hundreds of conditions and used coexpression analysis to distinguish variation in the dynamic pattern of gene expression from variation in expression levels. The majority of genes whose expression varied between the species maintained a conserved dynamic pattern. Cases of diverged dynamic pattern correspond to genes that were induced under distinct subsets of conditions in the two species. Profiling the interspecific hybrid allowed us to distinguish between genes with predominantly cis- or trans-regulatory variation. We find that trans-varying alleles are dominantly inherited, and that cis-variations are often complemented by variations in trans. Based on these results, we suggest that gene expression diverges primarily through changes in expression levels, but does not alter the pattern by which these levels are dynamically regulated.

Original languageEnglish
Pages (from-to)1000-1011
Number of pages12
JournalGenome Research
Volume30
DOIs
Publication statusPublished - 22 Jul 2020

Funding

We thank the Barkai laboratory members and the Levy laboratory members for helpful discussions. We thank Gil Hornung and Rotem Barzilay (The Nancy and Stephen Grand Israel National Center for Personalized Medicine [G-INCPM]) for implementing the dual-genome alignment pipeline. We thank Felix Jonas, Assaf Biran, Michal Chapal, Sagie Brodsky, Yoav Voichek, Anna Redgrave, and Patricia Wittkopp for critical reading and commenting on the manuscript. We thank Yael Maoz for proofreading. This project was supported by the U.S. National Science Foundation-U.S. Israel Binational Science Foundation-Molecular and Cellular Biosciences (NSF-BSF-MCB) (2019625), the Israel Science Foundation (ISF) (1738/15), and the Minerva center (AZ 57 46 9407 65). Author contributions: G.K., O.L., A.A.L., and N.B. designed the research. G.K. and O.L. performed experiments and analyzed the data. All authors contributed to the writing of the paper.

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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