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Published on: June 28, 2011
Tissue-specific and cis-regulatory changes underlie parallel, adaptive gene expression evolution in house mice
Sylvia M Durkin1, Mallory A Ballinger1, Michael W Nachman1
1Museum of Vertebrate Zoology and Department of Integrative Biology, University of California, Berkeley, Berkeley, California, United States of America.
Adaptive evolution in mice shows parallel gene expression changes driven by cis-regulatory alterations in tissue-specific genes. These findings illuminate early-stage gene regulatory evolution during divergence.
Area of Science:
- Evolutionary biology
- Genomics
- Molecular biology
Background:
- Gene regulation changes are key to adaptive evolution.
- The roles of cis- and trans-acting factors in short-term evolution are not fully understood.
- Studying parallel evolution can reveal mechanisms of divergence.
Purpose of the Study:
- To investigate gene expression patterns in mice adapted to different climates.
- To determine the relative contributions of cis- and trans-acting changes in early adaptive evolution.
- To assess the role of tissue-specific and cis-regulated genes in parallel evolution.
Main Methods:
- Comparative gene expression analysis in liver and brown adipose tissue of warm- and cold-adapted mouse strains.
- Allele-specific expression analysis in F1 hybrids.
- Integration of expression data with population genetic scans for selection.
Main Results:
- Parallel gene expression changes were observed more frequently than expected by chance.
- Expression evolution was predominantly linked to tissue-specific and cis-regulated genes.
- Genes under selection in natural populations showed parallelism and were enriched for cis-regulation, impacting traits like body size and immunity.
Conclusions:
- Parallel gene expression evolution in independently adapting mouse populations is largely driven by cis-regulatory changes.
- Tissue-specific regulation plays a significant role in early adaptive divergence.
- Cis-regulatory changes under selection influence key adaptive phenotypes.
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