Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.

BACKGROUND: Gene duplication is a major driver of evolutionary innovation as it allows for an organism to elaborate its existing biological functions via specialization or diversification of initially redundant gene paralogs. Gene function can diversify in several ways. Transcription factor gene par...

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Main Authors: Larry N Singh, Sridhar Hannenhalli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2394658?pdf=render
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author Larry N Singh
Sridhar Hannenhalli
author_facet Larry N Singh
Sridhar Hannenhalli
author_sort Larry N Singh
collection DOAJ
description BACKGROUND: Gene duplication is a major driver of evolutionary innovation as it allows for an organism to elaborate its existing biological functions via specialization or diversification of initially redundant gene paralogs. Gene function can diversify in several ways. Transcription factor gene paralogs in particular, can diversify either by changes in their tissue-specific expression pattern or by changes in the DNA binding site motif recognized by their protein product, which in turn alters their gene targets. The relationship between these two modes of functional diversification of transcription factor paralogs has not been previously investigated, and is essential for understanding adaptive evolution of transcription factor gene families. FINDINGS: Based on a large set of human paralogous transcription factor pairs, we show that when the DNA binding site motifs of transcription factor paralogs are similar, the expressions of the genes that encode the paralogs have diverged, so in general, at most one of the paralogs is highly expressed in a tissue. Moreover, paralogs with diverged DNA binding site motifs tend to be diverged in their function. Conversely, two paralogs that are highly expressed in a tissue tend to have dissimilar DNA binding site motifs. We have also found that in general, within a paralogous family, tissue-specific decrease in gene expression is more frequent than what is expected by chance. CONCLUSIONS: While previous investigations of paralogous gene diversification have only considered coding sequence divergence, by explicitly quantifying divergence in DNA binding site motif, our work presents a new paradigm for investigating functional diversification. Consistent with evolutionary expectation, our quantitative analysis suggests that paralogous transcription factors have survived extinction in part, either through diversification of their DNA binding site motifs or through alterations in their tissue-specific expression levels.
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spelling doaj.art-6652ea8929c847e9b02f7e2e3da6c42c2022-12-22T00:06:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-0136e234510.1371/journal.pone.0002345Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.Larry N SinghSridhar HannenhalliBACKGROUND: Gene duplication is a major driver of evolutionary innovation as it allows for an organism to elaborate its existing biological functions via specialization or diversification of initially redundant gene paralogs. Gene function can diversify in several ways. Transcription factor gene paralogs in particular, can diversify either by changes in their tissue-specific expression pattern or by changes in the DNA binding site motif recognized by their protein product, which in turn alters their gene targets. The relationship between these two modes of functional diversification of transcription factor paralogs has not been previously investigated, and is essential for understanding adaptive evolution of transcription factor gene families. FINDINGS: Based on a large set of human paralogous transcription factor pairs, we show that when the DNA binding site motifs of transcription factor paralogs are similar, the expressions of the genes that encode the paralogs have diverged, so in general, at most one of the paralogs is highly expressed in a tissue. Moreover, paralogs with diverged DNA binding site motifs tend to be diverged in their function. Conversely, two paralogs that are highly expressed in a tissue tend to have dissimilar DNA binding site motifs. We have also found that in general, within a paralogous family, tissue-specific decrease in gene expression is more frequent than what is expected by chance. CONCLUSIONS: While previous investigations of paralogous gene diversification have only considered coding sequence divergence, by explicitly quantifying divergence in DNA binding site motif, our work presents a new paradigm for investigating functional diversification. Consistent with evolutionary expectation, our quantitative analysis suggests that paralogous transcription factors have survived extinction in part, either through diversification of their DNA binding site motifs or through alterations in their tissue-specific expression levels.http://europepmc.org/articles/PMC2394658?pdf=render
spellingShingle Larry N Singh
Sridhar Hannenhalli
Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.
PLoS ONE
title Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.
title_full Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.
title_fullStr Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.
title_full_unstemmed Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.
title_short Functional diversification of paralogous transcription factors via divergence in DNA binding site motif and in expression.
title_sort functional diversification of paralogous transcription factors via divergence in dna binding site motif and in expression
url http://europepmc.org/articles/PMC2394658?pdf=render
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AT sridharhannenhalli functionaldiversificationofparalogoustranscriptionfactorsviadivergenceindnabindingsitemotifandinexpression