Cargando…

Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans

RNA interference (RNAi) pathways are widespread in metaozoans but the genes required show variable occurrence or activity in eukaryotic microbes, including many pathogens. While some Leishmania lack RNAi activity and Argonaute or Dicer genes, we show that Leishmania braziliensis and other species wi...

Descripción completa

Detalles Bibliográficos
Autores principales: Lye, Lon-Fye, Owens, Katherine, Shi, Huafang, Murta, Silvane M. F., Vieira, Ana Carolina, Turco, Salvatore J., Tschudi, Christian, Ullu, Elisabetta, Beverley, Stephen M.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965760/
https://www.ncbi.nlm.nih.gov/pubmed/21060810
http://dx.doi.org/10.1371/journal.ppat.1001161
_version_ 1782189539246211072
author Lye, Lon-Fye
Owens, Katherine
Shi, Huafang
Murta, Silvane M. F.
Vieira, Ana Carolina
Turco, Salvatore J.
Tschudi, Christian
Ullu, Elisabetta
Beverley, Stephen M.
author_facet Lye, Lon-Fye
Owens, Katherine
Shi, Huafang
Murta, Silvane M. F.
Vieira, Ana Carolina
Turco, Salvatore J.
Tschudi, Christian
Ullu, Elisabetta
Beverley, Stephen M.
author_sort Lye, Lon-Fye
collection PubMed
description RNA interference (RNAi) pathways are widespread in metaozoans but the genes required show variable occurrence or activity in eukaryotic microbes, including many pathogens. While some Leishmania lack RNAi activity and Argonaute or Dicer genes, we show that Leishmania braziliensis and other species within the Leishmania subgenus Viannia elaborate active RNAi machinery. Strong attenuation of expression from a variety of reporter and endogenous genes was seen. As expected, RNAi knockdowns of the sole Argonaute gene implicated this protein in RNAi. The potential for functional genetics was established by testing RNAi knockdown lines lacking the paraflagellar rod, a key component of the parasite flagellum. This sets the stage for the systematic manipulation of gene expression through RNAi in these predominantly diploid asexual organisms, and may also allow selective RNAi-based chemotherapy. Functional evolutionary surveys of RNAi genes established that RNAi activity was lost after the separation of the Leishmania subgenus Viannia from the remaining Leishmania species, a divergence associated with profound changes in the parasite infectious cycle and virulence. The genus Leishmania therefore offers an accessible system for testing hypothesis about forces that may select for the loss of RNAi during evolution, such as invasion by viruses, changes in genome plasticity mediated by transposable elements and gene amplification (including those mediating drug resistance), and/or alterations in parasite virulence.
format Text
id pubmed-2965760
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29657602010-11-08 Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans Lye, Lon-Fye Owens, Katherine Shi, Huafang Murta, Silvane M. F. Vieira, Ana Carolina Turco, Salvatore J. Tschudi, Christian Ullu, Elisabetta Beverley, Stephen M. PLoS Pathog Research Article RNA interference (RNAi) pathways are widespread in metaozoans but the genes required show variable occurrence or activity in eukaryotic microbes, including many pathogens. While some Leishmania lack RNAi activity and Argonaute or Dicer genes, we show that Leishmania braziliensis and other species within the Leishmania subgenus Viannia elaborate active RNAi machinery. Strong attenuation of expression from a variety of reporter and endogenous genes was seen. As expected, RNAi knockdowns of the sole Argonaute gene implicated this protein in RNAi. The potential for functional genetics was established by testing RNAi knockdown lines lacking the paraflagellar rod, a key component of the parasite flagellum. This sets the stage for the systematic manipulation of gene expression through RNAi in these predominantly diploid asexual organisms, and may also allow selective RNAi-based chemotherapy. Functional evolutionary surveys of RNAi genes established that RNAi activity was lost after the separation of the Leishmania subgenus Viannia from the remaining Leishmania species, a divergence associated with profound changes in the parasite infectious cycle and virulence. The genus Leishmania therefore offers an accessible system for testing hypothesis about forces that may select for the loss of RNAi during evolution, such as invasion by viruses, changes in genome plasticity mediated by transposable elements and gene amplification (including those mediating drug resistance), and/or alterations in parasite virulence. Public Library of Science 2010-10-28 /pmc/articles/PMC2965760/ /pubmed/21060810 http://dx.doi.org/10.1371/journal.ppat.1001161 Text en Lye et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lye, Lon-Fye
Owens, Katherine
Shi, Huafang
Murta, Silvane M. F.
Vieira, Ana Carolina
Turco, Salvatore J.
Tschudi, Christian
Ullu, Elisabetta
Beverley, Stephen M.
Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans
title Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans
title_full Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans
title_fullStr Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans
title_full_unstemmed Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans
title_short Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans
title_sort retention and loss of rna interference pathways in trypanosomatid protozoans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965760/
https://www.ncbi.nlm.nih.gov/pubmed/21060810
http://dx.doi.org/10.1371/journal.ppat.1001161
work_keys_str_mv AT lyelonfye retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT owenskatherine retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT shihuafang retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT murtasilvanemf retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT vieiraanacarolina retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT turcosalvatorej retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT tschudichristian retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT ulluelisabetta retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans
AT beverleystephenm retentionandlossofrnainterferencepathwaysintrypanosomatidprotozoans