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rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis
Primary biliary cholangitis (PBC) is a chronic, progressive cholestatic liver disease in which intrahepatic bile ducts are destroyed by an autoimmune reaction. Our previous genome-wide association study (GWAS) identified chromosome 11q23.1 as a susceptibility gene locus for PBC in the Japanese popul...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907150/ https://www.ncbi.nlm.nih.gov/pubmed/33633225 http://dx.doi.org/10.1038/s41598-021-84042-x |
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author | Hitomi, Yuki Aiba, Yoshihiro Kawai, Yosuke Kojima, Kaname Ueno, Kazuko Nishida, Nao Kawashima, Minae Gervais, Olivier Khor, Seik-Soon Nagasaki, Masao Tokunaga, Katsushi Nakamura, Minoru Tsuiji, Makoto |
author_facet | Hitomi, Yuki Aiba, Yoshihiro Kawai, Yosuke Kojima, Kaname Ueno, Kazuko Nishida, Nao Kawashima, Minae Gervais, Olivier Khor, Seik-Soon Nagasaki, Masao Tokunaga, Katsushi Nakamura, Minoru Tsuiji, Makoto |
author_sort | Hitomi, Yuki |
collection | PubMed |
description | Primary biliary cholangitis (PBC) is a chronic, progressive cholestatic liver disease in which intrahepatic bile ducts are destroyed by an autoimmune reaction. Our previous genome-wide association study (GWAS) identified chromosome 11q23.1 as a susceptibility gene locus for PBC in the Japanese population. Here, high-density association mapping based on single nucleotide polymorphism (SNP) imputation and in silico/in vitro functional analyses identified rs1944919 as the primary functional variant. Expression-quantitative trait loci analyses showed that the PBC susceptibility allele of rs1944919 was significantly associated with increased COLCA1/COLCA2 expression levels. Additionally, the effects of rs1944919 on COLCA1/COLCA2 expression levels were confirmed using genotype knock-in versions of cell lines constructed using the CRISPR/Cas9 system and differed between rs1944919-G/G clones and -T/T clones. To our knowledge, this is the first study to demonstrate the contribution of COLCA1/COLCA2 to PBC susceptibility. |
format | Online Article Text |
id | pubmed-7907150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79071502021-02-26 rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis Hitomi, Yuki Aiba, Yoshihiro Kawai, Yosuke Kojima, Kaname Ueno, Kazuko Nishida, Nao Kawashima, Minae Gervais, Olivier Khor, Seik-Soon Nagasaki, Masao Tokunaga, Katsushi Nakamura, Minoru Tsuiji, Makoto Sci Rep Article Primary biliary cholangitis (PBC) is a chronic, progressive cholestatic liver disease in which intrahepatic bile ducts are destroyed by an autoimmune reaction. Our previous genome-wide association study (GWAS) identified chromosome 11q23.1 as a susceptibility gene locus for PBC in the Japanese population. Here, high-density association mapping based on single nucleotide polymorphism (SNP) imputation and in silico/in vitro functional analyses identified rs1944919 as the primary functional variant. Expression-quantitative trait loci analyses showed that the PBC susceptibility allele of rs1944919 was significantly associated with increased COLCA1/COLCA2 expression levels. Additionally, the effects of rs1944919 on COLCA1/COLCA2 expression levels were confirmed using genotype knock-in versions of cell lines constructed using the CRISPR/Cas9 system and differed between rs1944919-G/G clones and -T/T clones. To our knowledge, this is the first study to demonstrate the contribution of COLCA1/COLCA2 to PBC susceptibility. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907150/ /pubmed/33633225 http://dx.doi.org/10.1038/s41598-021-84042-x Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hitomi, Yuki Aiba, Yoshihiro Kawai, Yosuke Kojima, Kaname Ueno, Kazuko Nishida, Nao Kawashima, Minae Gervais, Olivier Khor, Seik-Soon Nagasaki, Masao Tokunaga, Katsushi Nakamura, Minoru Tsuiji, Makoto rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis |
title | rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis |
title_full | rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis |
title_fullStr | rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis |
title_full_unstemmed | rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis |
title_short | rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis |
title_sort | rs1944919 on chromosome 11q23.1 and its effector genes colca1/colca2 confer susceptibility to primary biliary cholangitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907150/ https://www.ncbi.nlm.nih.gov/pubmed/33633225 http://dx.doi.org/10.1038/s41598-021-84042-x |
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