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Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota

Numerous host extrinsic and intrinsic factors affect the gut microbiota composition, but their cumulative effects do not sufficiently explain the variation in the microbiota, suggesting contributions of missing factors. The Japanese population possesses homogeneous genetic features suitable for geno...

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Autores principales: Ishida, Sachiko, Kato, Kumiko, Tanaka, Masami, Odamaki, Toshitaka, Kubo, Ryuichi, Mitsuyama, Eri, Xiao, Jin-zhong, Yamaguchi, Rui, Uematsu, Satoshi, Imoto, Seiya, Miyano, Satoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674416/
https://www.ncbi.nlm.nih.gov/pubmed/33208821
http://dx.doi.org/10.1038/s42003-020-01416-z
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author Ishida, Sachiko
Kato, Kumiko
Tanaka, Masami
Odamaki, Toshitaka
Kubo, Ryuichi
Mitsuyama, Eri
Xiao, Jin-zhong
Yamaguchi, Rui
Uematsu, Satoshi
Imoto, Seiya
Miyano, Satoru
author_facet Ishida, Sachiko
Kato, Kumiko
Tanaka, Masami
Odamaki, Toshitaka
Kubo, Ryuichi
Mitsuyama, Eri
Xiao, Jin-zhong
Yamaguchi, Rui
Uematsu, Satoshi
Imoto, Seiya
Miyano, Satoru
author_sort Ishida, Sachiko
collection PubMed
description Numerous host extrinsic and intrinsic factors affect the gut microbiota composition, but their cumulative effects do not sufficiently explain the variation in the microbiota, suggesting contributions of missing factors. The Japanese population possesses homogeneous genetic features suitable for genome-wide association study (GWAS). Here, we performed GWASs for human gut microbiota using 1068 healthy Japanese adults. To precisely evaluate genetic effects, we corrected for the impacts of numerous host extrinsic and demographic factors by introducing them as covariates, enabling us to discover five loci significantly associated with microbiome diversity measures: HS3ST4, C2CD2, 2p16.1, 10p15.1, and 18q12.2. Nevertheless, these five variants explain only a small fraction of the variation in the gut microbiota. We subsequently investigated the heritability of each of the 21 core genera and found that the abundances of six genera are heritable. We propose that the gut microbiota composition is affected by a highly polygenic architecture rather than several strongly associated variants in the Japanese population.
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spelling pubmed-76744162020-11-20 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota Ishida, Sachiko Kato, Kumiko Tanaka, Masami Odamaki, Toshitaka Kubo, Ryuichi Mitsuyama, Eri Xiao, Jin-zhong Yamaguchi, Rui Uematsu, Satoshi Imoto, Seiya Miyano, Satoru Commun Biol Article Numerous host extrinsic and intrinsic factors affect the gut microbiota composition, but their cumulative effects do not sufficiently explain the variation in the microbiota, suggesting contributions of missing factors. The Japanese population possesses homogeneous genetic features suitable for genome-wide association study (GWAS). Here, we performed GWASs for human gut microbiota using 1068 healthy Japanese adults. To precisely evaluate genetic effects, we corrected for the impacts of numerous host extrinsic and demographic factors by introducing them as covariates, enabling us to discover five loci significantly associated with microbiome diversity measures: HS3ST4, C2CD2, 2p16.1, 10p15.1, and 18q12.2. Nevertheless, these five variants explain only a small fraction of the variation in the gut microbiota. We subsequently investigated the heritability of each of the 21 core genera and found that the abundances of six genera are heritable. We propose that the gut microbiota composition is affected by a highly polygenic architecture rather than several strongly associated variants in the Japanese population. Nature Publishing Group UK 2020-11-18 /pmc/articles/PMC7674416/ /pubmed/33208821 http://dx.doi.org/10.1038/s42003-020-01416-z 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
Ishida, Sachiko
Kato, Kumiko
Tanaka, Masami
Odamaki, Toshitaka
Kubo, Ryuichi
Mitsuyama, Eri
Xiao, Jin-zhong
Yamaguchi, Rui
Uematsu, Satoshi
Imoto, Seiya
Miyano, Satoru
Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota
title Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota
title_full Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota
title_fullStr Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota
title_full_unstemmed Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota
title_short Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota
title_sort genome-wide association studies and heritability analysis reveal the involvement of host genetics in the japanese gut microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674416/
https://www.ncbi.nlm.nih.gov/pubmed/33208821
http://dx.doi.org/10.1038/s42003-020-01416-z
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