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A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation
We identified a non-synonymous mutation in Oas2 (I405N), a sensor of viral double-stranded RNA, from an ENU-mutagenesis screen designed to discover new genes involved in mammary development. The mutation caused post-partum failure of lactation in healthy mice with otherwise normally developed mammar...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695588/ https://www.ncbi.nlm.nih.gov/pubmed/29117179 http://dx.doi.org/10.1371/journal.pgen.1007072 |
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author | Oakes, Samantha R. Gallego-Ortega, David Stanford, Prudence M. Junankar, Simon Au, Wendy Wing Yee Kikhtyak, Zoya von Korff, Anita Sergio, Claudio M. Law, Andrew M. K. Castillo, Lesley E. Allerdice, Stephanie L. Young, Adelaide I. J. Piggin, Catherine Whittle, Belinda Bertram, Edward Naylor, Matthew J. Roden, Daniel L. Donovan, Jesse Korennykh, Alexei Goodnow, Christopher C. O’Bryan, Moira K. Ormandy, Christopher J. |
author_facet | Oakes, Samantha R. Gallego-Ortega, David Stanford, Prudence M. Junankar, Simon Au, Wendy Wing Yee Kikhtyak, Zoya von Korff, Anita Sergio, Claudio M. Law, Andrew M. K. Castillo, Lesley E. Allerdice, Stephanie L. Young, Adelaide I. J. Piggin, Catherine Whittle, Belinda Bertram, Edward Naylor, Matthew J. Roden, Daniel L. Donovan, Jesse Korennykh, Alexei Goodnow, Christopher C. O’Bryan, Moira K. Ormandy, Christopher J. |
author_sort | Oakes, Samantha R. |
collection | PubMed |
description | We identified a non-synonymous mutation in Oas2 (I405N), a sensor of viral double-stranded RNA, from an ENU-mutagenesis screen designed to discover new genes involved in mammary development. The mutation caused post-partum failure of lactation in healthy mice with otherwise normally developed mammary glands, characterized by greatly reduced milk protein synthesis coupled with epithelial cell death, inhibition of proliferation and a robust interferon response. Expression of mutant but not wild type Oas2 in cultured HC-11 or T47D mammary cells recapitulated the phenotypic and transcriptional effects observed in the mouse. The mutation activates the OAS2 pathway, demonstrated by a 34-fold increase in RNase L activity, and its effects were dependent on expression of RNase L and IRF7, proximal and distal pathway members. This is the first report of a viral recognition pathway regulating lactation. |
format | Online Article Text |
id | pubmed-5695588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56955882017-11-30 A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation Oakes, Samantha R. Gallego-Ortega, David Stanford, Prudence M. Junankar, Simon Au, Wendy Wing Yee Kikhtyak, Zoya von Korff, Anita Sergio, Claudio M. Law, Andrew M. K. Castillo, Lesley E. Allerdice, Stephanie L. Young, Adelaide I. J. Piggin, Catherine Whittle, Belinda Bertram, Edward Naylor, Matthew J. Roden, Daniel L. Donovan, Jesse Korennykh, Alexei Goodnow, Christopher C. O’Bryan, Moira K. Ormandy, Christopher J. PLoS Genet Research Article We identified a non-synonymous mutation in Oas2 (I405N), a sensor of viral double-stranded RNA, from an ENU-mutagenesis screen designed to discover new genes involved in mammary development. The mutation caused post-partum failure of lactation in healthy mice with otherwise normally developed mammary glands, characterized by greatly reduced milk protein synthesis coupled with epithelial cell death, inhibition of proliferation and a robust interferon response. Expression of mutant but not wild type Oas2 in cultured HC-11 or T47D mammary cells recapitulated the phenotypic and transcriptional effects observed in the mouse. The mutation activates the OAS2 pathway, demonstrated by a 34-fold increase in RNase L activity, and its effects were dependent on expression of RNase L and IRF7, proximal and distal pathway members. This is the first report of a viral recognition pathway regulating lactation. Public Library of Science 2017-11-08 /pmc/articles/PMC5695588/ /pubmed/29117179 http://dx.doi.org/10.1371/journal.pgen.1007072 Text en © 2017 Oakes 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Oakes, Samantha R. Gallego-Ortega, David Stanford, Prudence M. Junankar, Simon Au, Wendy Wing Yee Kikhtyak, Zoya von Korff, Anita Sergio, Claudio M. Law, Andrew M. K. Castillo, Lesley E. Allerdice, Stephanie L. Young, Adelaide I. J. Piggin, Catherine Whittle, Belinda Bertram, Edward Naylor, Matthew J. Roden, Daniel L. Donovan, Jesse Korennykh, Alexei Goodnow, Christopher C. O’Bryan, Moira K. Ormandy, Christopher J. A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
title | A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
title_full | A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
title_fullStr | A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
title_full_unstemmed | A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
title_short | A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
title_sort | mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695588/ https://www.ncbi.nlm.nih.gov/pubmed/29117179 http://dx.doi.org/10.1371/journal.pgen.1007072 |
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