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NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation
The brain is sensitive to the dose of MeCP2 such that small fluctuations in protein quantity lead to neuropsychiatric disease. Despite the importance of MeCP2 levels to brain function, little is known about its regulation. In this study, we report eleven individuals with neuropsychiatric disease and...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586391/ https://www.ncbi.nlm.nih.gov/pubmed/26312503 http://dx.doi.org/10.7554/eLife.10782 |
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author | Gennarino, Vincenzo A Alcott, Callison E Chen, Chun-An Chaudhury, Arindam Gillentine, Madelyn A Rosenfeld, Jill A Parikh, Sumit Wheless, James W Roeder, Elizabeth R Horovitz, Dafne DG Roney, Erin K Smith, Janice L Cheung, Sau W Li, Wei Neilson, Joel R Schaaf, Christian P Zoghbi, Huda Y |
author_facet | Gennarino, Vincenzo A Alcott, Callison E Chen, Chun-An Chaudhury, Arindam Gillentine, Madelyn A Rosenfeld, Jill A Parikh, Sumit Wheless, James W Roeder, Elizabeth R Horovitz, Dafne DG Roney, Erin K Smith, Janice L Cheung, Sau W Li, Wei Neilson, Joel R Schaaf, Christian P Zoghbi, Huda Y |
author_sort | Gennarino, Vincenzo A |
collection | PubMed |
description | The brain is sensitive to the dose of MeCP2 such that small fluctuations in protein quantity lead to neuropsychiatric disease. Despite the importance of MeCP2 levels to brain function, little is known about its regulation. In this study, we report eleven individuals with neuropsychiatric disease and copy-number variations spanning NUDT21, which encodes a subunit of pre-mRNA cleavage factor Im. Investigations of MECP2 mRNA and protein abundance in patient-derived lymphoblastoid cells from one NUDT21 deletion and three duplication cases show that NUDT21 regulates MeCP2 protein quantity. Elevated NUDT21 increases usage of the distal polyadenylation site in the MECP2 3′ UTR, resulting in an enrichment of inefficiently translated long mRNA isoforms. Furthermore, normalization of NUDT21 via siRNA-mediated knockdown in duplication patient lymphoblasts restores MeCP2 to normal levels. Ultimately, we identify NUDT21 as a novel candidate for intellectual disability and neuropsychiatric disease, and elucidate a mechanism of pathogenesis by MeCP2 dysregulation via altered alternative polyadenylation. DOI: http://dx.doi.org/10.7554/eLife.10782.001 |
format | Online Article Text |
id | pubmed-4586391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45863912015-09-30 NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation Gennarino, Vincenzo A Alcott, Callison E Chen, Chun-An Chaudhury, Arindam Gillentine, Madelyn A Rosenfeld, Jill A Parikh, Sumit Wheless, James W Roeder, Elizabeth R Horovitz, Dafne DG Roney, Erin K Smith, Janice L Cheung, Sau W Li, Wei Neilson, Joel R Schaaf, Christian P Zoghbi, Huda Y eLife Neuroscience The brain is sensitive to the dose of MeCP2 such that small fluctuations in protein quantity lead to neuropsychiatric disease. Despite the importance of MeCP2 levels to brain function, little is known about its regulation. In this study, we report eleven individuals with neuropsychiatric disease and copy-number variations spanning NUDT21, which encodes a subunit of pre-mRNA cleavage factor Im. Investigations of MECP2 mRNA and protein abundance in patient-derived lymphoblastoid cells from one NUDT21 deletion and three duplication cases show that NUDT21 regulates MeCP2 protein quantity. Elevated NUDT21 increases usage of the distal polyadenylation site in the MECP2 3′ UTR, resulting in an enrichment of inefficiently translated long mRNA isoforms. Furthermore, normalization of NUDT21 via siRNA-mediated knockdown in duplication patient lymphoblasts restores MeCP2 to normal levels. Ultimately, we identify NUDT21 as a novel candidate for intellectual disability and neuropsychiatric disease, and elucidate a mechanism of pathogenesis by MeCP2 dysregulation via altered alternative polyadenylation. DOI: http://dx.doi.org/10.7554/eLife.10782.001 eLife Sciences Publications, Ltd 2015-08-27 /pmc/articles/PMC4586391/ /pubmed/26312503 http://dx.doi.org/10.7554/eLife.10782 Text en © 2015, Gennarino et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Gennarino, Vincenzo A Alcott, Callison E Chen, Chun-An Chaudhury, Arindam Gillentine, Madelyn A Rosenfeld, Jill A Parikh, Sumit Wheless, James W Roeder, Elizabeth R Horovitz, Dafne DG Roney, Erin K Smith, Janice L Cheung, Sau W Li, Wei Neilson, Joel R Schaaf, Christian P Zoghbi, Huda Y NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
title | NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
title_full | NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
title_fullStr | NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
title_full_unstemmed | NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
title_short | NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
title_sort | nudt21-spanning cnvs lead to neuropsychiatric disease and altered mecp2 abundance via alternative polyadenylation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586391/ https://www.ncbi.nlm.nih.gov/pubmed/26312503 http://dx.doi.org/10.7554/eLife.10782 |
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