Background Selection at the Chitin Synthase II (chs2) Locus in Paracoccidioides Brasiliensis Species Complex
ABSTRACT: In fungi, chitin synthases have been classified into five classes according to differences in regions of high sequence conservation. The current investigation was initiated to examine the causes for the polymorphism patterns found in a class II chitin synthase gene (chs2) of Paracoccidioid...
- Autores:
-
Matute González, Daniel Ricardo
Torres Gómez, Isaura Patricia
Salgado Salazar, Catalina
Restrepo Moreno, Angela
McEwen Ochoa, Juan Guillermo
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2007
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/33214
- Acceso en línea:
- https://hdl.handle.net/10495/33214
https://www.sciencedirect.com/science/article/pii/S1087184507000114
- Palabra clave:
- Paracoccidioides
Paracoccidioides
Chitin Synthase
Quitina Sintasa
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc-nd/2.5/co/
Summary: | ABSTRACT: In fungi, chitin synthases have been classified into five classes according to differences in regions of high sequence conservation. The current investigation was initiated to examine the causes for the polymorphism patterns found in a class II chitin synthase gene (chs2) of Paracoccidioides brasiliensis, in an attempt to determine the evolutionary forces affecting the chitin synthesis metabolic pathway. Neutrality tests were applied to the chs2 sequences exhibited by P. brasiliensis species complex. According to these tests and based on non-synonymous differences, P. brasiliensis data rejected the null hypothesis for a pure drift mutational process owing to a large excess of unique polymorphisms. In contrast, the synonymous and intron site differences did not reject the null hypothesis. This pattern appears consistent with weak selection against most amino acid changes, in which the effect of background selection was not detectable at synonymous nor at intron sites. |
---|