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Exome Sequencing in Individuals with Isolated Biliary Atresia

Biliary atresia (BA) is a severe pediatric liver disease resulting in necroinflammatory obliteration of the extrahepatic biliary tree. BA presents within the first few months of life as either an isolated finding or with additional syndromic features. The etiology of isolated BA is unknown, with evi...

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Autores principales: Rajagopalan, Ramakrishnan, Tsai, Ellen A., Grochowski, Christopher M., Kelly, Susan M., Loomes, Kathleen M., Spinner, Nancy B., Devoto, Marcella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026070/
https://www.ncbi.nlm.nih.gov/pubmed/32066793
http://dx.doi.org/10.1038/s41598-020-59379-4
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author Rajagopalan, Ramakrishnan
Tsai, Ellen A.
Grochowski, Christopher M.
Kelly, Susan M.
Loomes, Kathleen M.
Spinner, Nancy B.
Devoto, Marcella
author_facet Rajagopalan, Ramakrishnan
Tsai, Ellen A.
Grochowski, Christopher M.
Kelly, Susan M.
Loomes, Kathleen M.
Spinner, Nancy B.
Devoto, Marcella
author_sort Rajagopalan, Ramakrishnan
collection PubMed
description Biliary atresia (BA) is a severe pediatric liver disease resulting in necroinflammatory obliteration of the extrahepatic biliary tree. BA presents within the first few months of life as either an isolated finding or with additional syndromic features. The etiology of isolated BA is unknown, with evidence for infectious, environmental, and genetic risk factors described. However, to date, there are no definitive causal genes identified for isolated BA in humans, and the question of whether single gene defects play a major role remains open. We performed exome-sequencing in 101 North American patients of European descent with isolated BA (including 30 parent-child trios) and considered several experimental designs to identify potentially deleterious protein-altering variants that may be involved in the disease. In a case-only analysis, we did not identify genes with variants shared among more than two probands, and burden tests of rare variants using a case-case control design did not yield significant results. In the trio analysis of 30 simplex families (patient and parent trios), we identified 66 de novo variants in 66 genes including potentially deleterious variants in STIP1 and REV1. STIP1 is a co-chaperone for the heat-shock protein, HSP90, and has been shown to have diverse functions in yeast, flies and mammals, including stress-responses. REV1 is known to be a key player in DNA repair pathway and to interact with HSP90. In conclusion, our results do not support the hypothesis that a simple genetic model is responsible for the majority of cases of isolated BA. Our finding of de novo variants in genes linked to evolutionarily conserved stress responses (STIP1 and REV1) suggests that exploration of how genetic susceptibility and environmental exposure may interact to cause BA is warranted.
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spelling pubmed-70260702020-02-24 Exome Sequencing in Individuals with Isolated Biliary Atresia Rajagopalan, Ramakrishnan Tsai, Ellen A. Grochowski, Christopher M. Kelly, Susan M. Loomes, Kathleen M. Spinner, Nancy B. Devoto, Marcella Sci Rep Article Biliary atresia (BA) is a severe pediatric liver disease resulting in necroinflammatory obliteration of the extrahepatic biliary tree. BA presents within the first few months of life as either an isolated finding or with additional syndromic features. The etiology of isolated BA is unknown, with evidence for infectious, environmental, and genetic risk factors described. However, to date, there are no definitive causal genes identified for isolated BA in humans, and the question of whether single gene defects play a major role remains open. We performed exome-sequencing in 101 North American patients of European descent with isolated BA (including 30 parent-child trios) and considered several experimental designs to identify potentially deleterious protein-altering variants that may be involved in the disease. In a case-only analysis, we did not identify genes with variants shared among more than two probands, and burden tests of rare variants using a case-case control design did not yield significant results. In the trio analysis of 30 simplex families (patient and parent trios), we identified 66 de novo variants in 66 genes including potentially deleterious variants in STIP1 and REV1. STIP1 is a co-chaperone for the heat-shock protein, HSP90, and has been shown to have diverse functions in yeast, flies and mammals, including stress-responses. REV1 is known to be a key player in DNA repair pathway and to interact with HSP90. In conclusion, our results do not support the hypothesis that a simple genetic model is responsible for the majority of cases of isolated BA. Our finding of de novo variants in genes linked to evolutionarily conserved stress responses (STIP1 and REV1) suggests that exploration of how genetic susceptibility and environmental exposure may interact to cause BA is warranted. Nature Publishing Group UK 2020-02-17 /pmc/articles/PMC7026070/ /pubmed/32066793 http://dx.doi.org/10.1038/s41598-020-59379-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rajagopalan, Ramakrishnan
Tsai, Ellen A.
Grochowski, Christopher M.
Kelly, Susan M.
Loomes, Kathleen M.
Spinner, Nancy B.
Devoto, Marcella
Exome Sequencing in Individuals with Isolated Biliary Atresia
title Exome Sequencing in Individuals with Isolated Biliary Atresia
title_full Exome Sequencing in Individuals with Isolated Biliary Atresia
title_fullStr Exome Sequencing in Individuals with Isolated Biliary Atresia
title_full_unstemmed Exome Sequencing in Individuals with Isolated Biliary Atresia
title_short Exome Sequencing in Individuals with Isolated Biliary Atresia
title_sort exome sequencing in individuals with isolated biliary atresia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026070/
https://www.ncbi.nlm.nih.gov/pubmed/32066793
http://dx.doi.org/10.1038/s41598-020-59379-4
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