Escherichia coli transcription factors of unknown function: sequence features and possible evolutionary relationships

Author:

Duarte-Velázquez Isabel1,de la Mora Javier2,Ramírez-Prado Jorge Humberto3ORCID,Aguillón-Bárcenas Alondra1,Tornero-Gutiérrez Fátima1,Cordero-Loreto Eugenia1,Anaya-Velázquez Fernando1,Páramo-Pérez Itzel1,Rangel-Serrano Ángeles1,Muñoz-Carranza Sergio Rodrigo1,Romero-González Oscar Eduardo1,Cardoso-Reyes Luis Rafael1,Rodríguez-Ojeda Ricardo Alberto1,Mora-Montes Héctor Manuel1ORCID,Vargas-Maya Naurú Idalia1,Padilla-Vaca Felipe1,Franco Bernardo1ORCID

Affiliation:

1. Biology, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Guanajuato, Guanajuato, México

2. Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autonoma de Mexico, Mexico City, México

3. Unidad de Biotecnología, Centro de Investigación Científica de Yucatán, A. C., Mérida, Yucatán, Mexico

Abstract

Organisms need mechanisms to perceive the environment and respond accordingly to environmental changes or the presence of hazards. Transcription factors (TFs) are required for cells to respond to the environment by controlling the expression of genes needed. Escherichia coli has been the model bacterium for many decades, and still, there are features embedded in its genome that remain unstudied. To date, 58 TFs remain poorly characterized, although their binding sites have been experimentally determined. This study showed that these TFs have sequence variation at the third codon position G+C content but maintain the same Codon Adaptation Index (CAI) trend as annotated functional transcription factors. Most of these transcription factors are in areas of the genome where abundant repetitive and mobile elements are present. Sequence divergence points to groups with distinctive sequence signatures but maintaining the same type of DNA binding domain. Finally, the analysis of the promoter sequences of the 58 TFs showed A+T rich regions that agree with the features of horizontally transferred genes. The findings reported here pave the way for future research of these TFs that may uncover their role as spare factors in case of lose-of-function mutations in core TFs and trace back their evolutionary history.

Funder

CONACyT

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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