Skip Navigation


MBE Advance Access originally published online on October 5, 2007
Molecular Biology and Evolution 2007 24(12):2816-2826; doi:10.1093/molbev/msm216
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Material
Right arrow All Versions of this Article:
24/12/2816    most recent
msm216v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Streisfeld, M. A.
Right arrow Articles by Rausher, M. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Streisfeld, M. A.
Right arrow Articles by Rausher, M. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2007. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Research Articles

Relaxed Constraint and Evolutionary Rate Variation between Basic Helix-Loop-Helix Floral Anthocyanin Regulators in Ipomoea

Matthew A. Streisfeld and Mark D. Rausher

Department of Biology, Duke University, Durham, NC

E-mail: mstreisf{at}duke.edu.

Accepted for publication September 27, 2007.

Regulatory genes are believed to play a large role in morphological diversification and are often characterized by elevated rates of evolution. Whether this rapid evolution is primarily due to adaptive differentiation or relaxed selective constraint remains an open question. We attempted to distinguish between these alternative outcomes in 2 transcription factors known to regulate the expression of anthocyanin pigmentation genes in flowers. We cloned the full-length coding region from 2 basic helix-loop-helix transcription factors from several species of Ipomoea with diverse flower colors and determined the selective forces operating on them. In both genes, rapidly evolving sites and indel mutations are clustered in nonbinding domains, but the extent of rate acceleration in these domains is reduced relative to most previously characterized plant transcription factors. Moreover, codon models of substitution rates and models evaluating the magnitude of change to physical amino acid properties demonstrate little evidence for adaptive evolution and suggest that elevated nonsynonymous substitution rates in these domains represent relaxed selective constraint. Although both genes show qualitatively similar patterns, their rates of evolution differ significantly due to an increased rate of nonsynonymous substitutions in the nonbinding domains in one copy, suggesting substantial differences in functional constraint on each gene. In general, these results provide additional evidence demonstrating that decreased constraint as opposed to positive selection is largely responsible for the frequently observed pattern of rapid evolution in particular domains of plant transcription factors. More specifically, they suggest that most of the amino acid substitutions are neutral and do not implicate a role for natural selection on these regulatory genes in the diversification of flower color in Ipomoea.

Key Words: Ipomoea • positive selection • rate variation • anthocyanin • basic helix-loop-helix • transcription factor


Patricia Beldade, Associate Editor


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.