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Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation

Mammalian Argonaute proteins (EIF2C1−4) play an essential role in RNA-induced silencing. Here, we show that the loss of eIF2C2 (Argonaute2 or Ago2) results in gastrulation arrest, ectopic expression of Brachyury (T), and mesoderm expansion. We identify a genetic interaction between Ago2 and T, as Ag...

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Detalles Bibliográficos
Autores principales: Alisch, Reid S, Jin, Peng, Epstein, Michael, Caspary, Tamara, Warren, Stephen T
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323323/
https://www.ncbi.nlm.nih.gov/pubmed/18166081
http://dx.doi.org/10.1371/journal.pgen.0030227
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author Alisch, Reid S
Jin, Peng
Epstein, Michael
Caspary, Tamara
Warren, Stephen T
author_facet Alisch, Reid S
Jin, Peng
Epstein, Michael
Caspary, Tamara
Warren, Stephen T
author_sort Alisch, Reid S
collection PubMed
description Mammalian Argonaute proteins (EIF2C1−4) play an essential role in RNA-induced silencing. Here, we show that the loss of eIF2C2 (Argonaute2 or Ago2) results in gastrulation arrest, ectopic expression of Brachyury (T), and mesoderm expansion. We identify a genetic interaction between Ago2 and T, as Ago2 haploinsufficiency partially rescues the classic T/+ short-tail phenotype. Finally, we demonstrate that the ectopic T expression and concomitant mesoderm expansion result from disrupted fibroblast growth factor signaling, likely due to aberrant expression of Eomesodermin. Together, these data indicate that a factor best known as a key component of the RNA-induced silencing complex is required for proper fibroblast growth factor signaling during gastrulation, suggesting a possible micro-RNA function in the formation of a mammalian germ layer.
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spelling pubmed-23233232008-04-18 Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation Alisch, Reid S Jin, Peng Epstein, Michael Caspary, Tamara Warren, Stephen T PLoS Genet Research Article Mammalian Argonaute proteins (EIF2C1−4) play an essential role in RNA-induced silencing. Here, we show that the loss of eIF2C2 (Argonaute2 or Ago2) results in gastrulation arrest, ectopic expression of Brachyury (T), and mesoderm expansion. We identify a genetic interaction between Ago2 and T, as Ago2 haploinsufficiency partially rescues the classic T/+ short-tail phenotype. Finally, we demonstrate that the ectopic T expression and concomitant mesoderm expansion result from disrupted fibroblast growth factor signaling, likely due to aberrant expression of Eomesodermin. Together, these data indicate that a factor best known as a key component of the RNA-induced silencing complex is required for proper fibroblast growth factor signaling during gastrulation, suggesting a possible micro-RNA function in the formation of a mammalian germ layer. Public Library of Science 2007-12 2007-12-28 /pmc/articles/PMC2323323/ /pubmed/18166081 http://dx.doi.org/10.1371/journal.pgen.0030227 Text en © 2007 Alisch 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
Alisch, Reid S
Jin, Peng
Epstein, Michael
Caspary, Tamara
Warren, Stephen T
Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
title Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
title_full Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
title_fullStr Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
title_full_unstemmed Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
title_short Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
title_sort argonaute2 is essential for mammalian gastrulation and proper mesoderm formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323323/
https://www.ncbi.nlm.nih.gov/pubmed/18166081
http://dx.doi.org/10.1371/journal.pgen.0030227
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