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Experimental evidence for negative selection in the evolution of a Yersinia pestis pseudogene.


ABSTRACT: Yersinia pestis, the agent of bubonic plague, evolved from the enteric pathogen Yersinia pseudotuberculosis within the past 20,000 years. Because ancestor and descendant both exist, it is possible to infer steps in molecular evolution by direct experimental approaches. The Y. pestis life cycle includes establishment of a biofilm within its vector, the flea. Although Y. pseudotuberculosis makes biofilms in other environments, it fails to do so in the insect. We show that rcsA, a negative regulator of biofilms that is functional in Y. pseudotuberculosis, is a pseudogene in Y. pestis. Replacement of the pseudogene with the functional Y. pseudotuberculosis rcsA allele strongly represses biofilm formation and essentially abolishes flea biofilms. The conversion of rcsA to a pseudogene during Y. pestis evolution, therefore, was a case of negative selection rather than neutral genetic drift.

SUBMITTER: Sun YC 

PROVIDER: S-EPMC2430365 | biostudies-literature | 2008 Jun

REPOSITORIES: biostudies-literature

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Experimental evidence for negative selection in the evolution of a Yersinia pestis pseudogene.

Sun Yi-Cheng YC   Hinnebusch B Joseph BJ   Darby Creg C  

Proceedings of the National Academy of Sciences of the United States of America 20080603 23


Yersinia pestis, the agent of bubonic plague, evolved from the enteric pathogen Yersinia pseudotuberculosis within the past 20,000 years. Because ancestor and descendant both exist, it is possible to infer steps in molecular evolution by direct experimental approaches. The Y. pestis life cycle includes establishment of a biofilm within its vector, the flea. Although Y. pseudotuberculosis makes biofilms in other environments, it fails to do so in the insect. We show that rcsA, a negative regulato  ...[more]

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