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In silico prediction of secretory proteins of Opisthorchis viverrini, Clonorchis sinensis and Fasciola hepatica that target the host cell nucleus

  • Claudia Machicado
  • , Maria Pia Soto
  • , Luis Felipe La Chira
  • , Joel Torres
  • , Carlos Mendoza
  • , Luis A. Marcos
  • University of Zaragoza
  • Universidad Peruana Cayetano Heredia
  • Universidad Católica de Santa María
  • Univ. Nacional Mayor de San Marcos
  • Universidad Nacional de Trujillo
  • Stony Brook University School of Medicine

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

2 Citas (Scopus)

Resumen

Liver flukes Fasciola hepatica, Opisthorchis viverrini and Clonorchis sinensis are causing agents of liver and hepatobiliary diseases. A remarkable difference between such worms is the fact that O. viverrini and C. sinensis are carcinogenic organisms whereas F. hepatica is not carcinogenic. The release of secretory factors by carcinogenic flukes seems to contribute to cancer development however if some of these target the host cell nuclei is unknown. We investigated the existence of O. viverrini and C. sinensis secretory proteins that target the nucleus of host cells and compared these with the corresponding proteins predicted in F. hepatica. Here we applied an algorithm composed by in silico approaches that screened and analyzed the potential genes predicted from genomes of liver flukes. We found 31 and 22 secretory proteins that target the nucleus of host cells in O. viverrini and C. sinensis, respectively, and that have no homologs in F. hepatica. These polypeptides have enriched the transcription initiation process and nucleic acid binding in O. viverrini and C. sinensis, respectively. In addition, other 11 secretory proteins of O. viverrini and C. sinensis, that target the nucleus of host cells, had F. hepatica homologs, have enriched RNA processing function. In conclusion, O. viverrini and C. sinensis have 31 and 22 genes, respectively, that may be involved in their carcinogenic action through a direct targeting on the host cell nuclei.

Idioma originalInglés
Número de artículoe07204
PublicaciónHeliyon
Volumen7
N.º7
DOI
EstadoPublicada - jul. 2021

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Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

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