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A long noncoding RNA promotes parasite differentiation in African trypanosomes

The parasite Trypanosoma brucei causes African sleeping sickness that is fatal to patients if untreated. Parasite differentiation from a replicative slender form into a quiescent stumpy form promotes host survival and parasite transmission. Long noncoding RNAs (lncRNAs) are known to regulate cell di...

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Autores principales: Guegan, Fabien, Rajan, K. Shanmugha, Bento, Fábio, Pinto-Neves, Daniel, Sequeira, Mariana, Gumińska, Natalia, Mroczek, Seweryn, Dziembowski, Andrzej, Cohen-Chalamish, Smadar, Doniger, Tirza, Galili, Beathrice, Estévez, Antonio M., Notredame, Cedric, Michaeli, Shulamit, Figueiredo, Luisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200285/
https://www.ncbi.nlm.nih.gov/pubmed/35704590
http://dx.doi.org/10.1126/sciadv.abn2706
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author Guegan, Fabien
Rajan, K. Shanmugha
Bento, Fábio
Pinto-Neves, Daniel
Sequeira, Mariana
Gumińska, Natalia
Mroczek, Seweryn
Dziembowski, Andrzej
Cohen-Chalamish, Smadar
Doniger, Tirza
Galili, Beathrice
Estévez, Antonio M.
Notredame, Cedric
Michaeli, Shulamit
Figueiredo, Luisa M.
author_facet Guegan, Fabien
Rajan, K. Shanmugha
Bento, Fábio
Pinto-Neves, Daniel
Sequeira, Mariana
Gumińska, Natalia
Mroczek, Seweryn
Dziembowski, Andrzej
Cohen-Chalamish, Smadar
Doniger, Tirza
Galili, Beathrice
Estévez, Antonio M.
Notredame, Cedric
Michaeli, Shulamit
Figueiredo, Luisa M.
author_sort Guegan, Fabien
collection PubMed
description The parasite Trypanosoma brucei causes African sleeping sickness that is fatal to patients if untreated. Parasite differentiation from a replicative slender form into a quiescent stumpy form promotes host survival and parasite transmission. Long noncoding RNAs (lncRNAs) are known to regulate cell differentiation in other eukaryotes. To determine whether lncRNAs are also involved in parasite differentiation, we used RNA sequencing to survey the T. brucei genome, identifying 1428 previously uncharacterized lncRNA genes. We find that grumpy lncRNA is a key regulator that promotes parasite differentiation into the quiescent stumpy form. This function is promoted by a small nucleolar RNA encoded within the grumpy lncRNA. snoGRUMPY binds to messenger RNAs of at least two stumpy regulatory genes, promoting their expression. grumpy overexpression reduces parasitemia in infected mice. Our analyses suggest that T. brucei lncRNAs modulate parasite-host interactions and provide a mechanism by which grumpy regulates cell differentiation in trypanosomes.
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spelling pubmed-92002852022-06-27 A long noncoding RNA promotes parasite differentiation in African trypanosomes Guegan, Fabien Rajan, K. Shanmugha Bento, Fábio Pinto-Neves, Daniel Sequeira, Mariana Gumińska, Natalia Mroczek, Seweryn Dziembowski, Andrzej Cohen-Chalamish, Smadar Doniger, Tirza Galili, Beathrice Estévez, Antonio M. Notredame, Cedric Michaeli, Shulamit Figueiredo, Luisa M. Sci Adv Biomedicine and Life Sciences The parasite Trypanosoma brucei causes African sleeping sickness that is fatal to patients if untreated. Parasite differentiation from a replicative slender form into a quiescent stumpy form promotes host survival and parasite transmission. Long noncoding RNAs (lncRNAs) are known to regulate cell differentiation in other eukaryotes. To determine whether lncRNAs are also involved in parasite differentiation, we used RNA sequencing to survey the T. brucei genome, identifying 1428 previously uncharacterized lncRNA genes. We find that grumpy lncRNA is a key regulator that promotes parasite differentiation into the quiescent stumpy form. This function is promoted by a small nucleolar RNA encoded within the grumpy lncRNA. snoGRUMPY binds to messenger RNAs of at least two stumpy regulatory genes, promoting their expression. grumpy overexpression reduces parasitemia in infected mice. Our analyses suggest that T. brucei lncRNAs modulate parasite-host interactions and provide a mechanism by which grumpy regulates cell differentiation in trypanosomes. American Association for the Advancement of Science 2022-06-15 /pmc/articles/PMC9200285/ /pubmed/35704590 http://dx.doi.org/10.1126/sciadv.abn2706 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Guegan, Fabien
Rajan, K. Shanmugha
Bento, Fábio
Pinto-Neves, Daniel
Sequeira, Mariana
Gumińska, Natalia
Mroczek, Seweryn
Dziembowski, Andrzej
Cohen-Chalamish, Smadar
Doniger, Tirza
Galili, Beathrice
Estévez, Antonio M.
Notredame, Cedric
Michaeli, Shulamit
Figueiredo, Luisa M.
A long noncoding RNA promotes parasite differentiation in African trypanosomes
title A long noncoding RNA promotes parasite differentiation in African trypanosomes
title_full A long noncoding RNA promotes parasite differentiation in African trypanosomes
title_fullStr A long noncoding RNA promotes parasite differentiation in African trypanosomes
title_full_unstemmed A long noncoding RNA promotes parasite differentiation in African trypanosomes
title_short A long noncoding RNA promotes parasite differentiation in African trypanosomes
title_sort long noncoding rna promotes parasite differentiation in african trypanosomes
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200285/
https://www.ncbi.nlm.nih.gov/pubmed/35704590
http://dx.doi.org/10.1126/sciadv.abn2706
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