Why highly expressed proteins evolve slowly
Abstract
Much recent work has explored molecular and population-genetic constraints on the rate of protein sequence evolution. The best predictor of evolutionary rate is expression level, for reasons that have remained unexplained. Here, we hypothesize that selection to reduce the burden of protein misfolding will favor protein sequences with increased robustness to translational missense errors. Pressure for translational robustness increases with expression level and constrains sequence evolution. Using several sequenced yeast genomes, global expression and protein abundance data, and sets of paralogs traceable to an ancient whole-genome duplication in yeast, we rule out several confounding effects and show that expression level explains roughly half the variation in Saccharomyces cerevisiae protein evolutionary rates. We examine causes for expression's dominant role and find that genome-wide tests favor the translational robustness explanation over existing hypotheses that invoke constraints on function or translational efficiency. Our results suggest that proteins evolve at rates largely unrelated to their functions and can explain why highly expressed proteins evolve slowly across the tree of life.
Additional Information
© 2005 by the National Academy of Sciences Edited by Francisco J. Ayala, University of California, Irvine, CA, and approved August 11, 2005 (received for review May 16, 2005). Published online before print September 21, 2005, 10.1073/pnas.0504070102 This work was supported by National Institutes of Health National Research Service Award 5 T32 MH19138 (to D.A.D.) and a Howard Hughes Medical Institute Predoctoral Fellowship (to J.D.B.). Author contributions: D.A.D. designed and performed research; D.A.D., J.D.B., C.A., C.O.W., and F.H.A. contributed new reagents/analytic tools; D.A.D. analyzed data; and D.A.D., J.D.B., C.A., C.O.W., and F.H.A. wrote the paper. This paper was submitted directly (Track II) to the PNAS office.Attached Files
Published - DRUpnas05b.pdf
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Additional details
- PMCID
- PMC1242296
- Eprint ID
- 2221
- Resolver ID
- CaltechAUTHORS:DRUpnas05b
- NIH Predoctoral Fellowship
- 5 T32 MH19138
- Howard Hughes Medical Institute (HHMI)
- Created
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2006-03-21Created from EPrint's datestamp field
- Updated
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2023-06-01Created from EPrint's last_modified field