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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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