The Genetic Architecture of Murine Glutathione Transferases

Glutathione S-transferase (GST) genes play a protective role against oxidative stress and may influence disease risk and drug pharmacokinetics. In this study, massive multiscalar trait profiling across a large population of mice derived from a cross between C57BL/6J (B6) and DBA2/J (D2)—the BXD f...

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Tác giả chính: Lu Lu, Ashutosh, K Pandey, M Trevor, Houseal, Megan, K Mulligan
Ngôn ngữ:English
Năm xuất bản: Public Library of Science (PLoS) 2018
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Truy cập Trực tuyến:http://lrc.quangbinhuni.edu.vn:8181/dspace/handle/DHQB_123456789/3841
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spelling oai:localhost:DHQB_123456789-38412018-10-22T08:44:32Z The Genetic Architecture of Murine Glutathione Transferases Lu Lu Ashutosh, K Pandey M Trevor, Houseal Megan, K Mulligan The Genetic Architecture Murine Glutathione Transferases Glutathione S-transferase Glutathione S-transferase (GST) genes play a protective role against oxidative stress and may influence disease risk and drug pharmacokinetics. In this study, massive multiscalar trait profiling across a large population of mice derived from a cross between C57BL/6J (B6) and DBA2/J (D2)—the BXD family—was combined with linkage and bioinformatic analyses to characterize mechanisms controlling GST expression and to identify downstream consequences of this variation. Similar to humans, mice show a wide range in expression of GST family members. Variation in the expression of Gsta4, Gstt2, Gstz1, Gsto1, and Mgst3 is modulated by local expression QTLs (eQTLs) in several tissues. Higher expression of Gsto1 in brain and liver of BXD strains is strongly associated (P < 0.01) with inheritance of the B6 parental allele whereas higher expression of Gsta4 and Mgst3 in brain and liver, and Gstt2 and Gstz1 in brain is strongly associated with inheritance of the D2 parental allele. Allele-specific assays confirmed that expression of Gsto1, Gsta4, and Mgst3 are modulated by sequence variants within or near each gene locus. We exploited this endogenous variation to identify coexpression networks and downstream targets in mouse and human. Through a combined systems genetics approach, we provide new insight into the biological role of naturally occurring variants in GST genes. 2018-08-23T07:38:55Z 2018-08-23T07:38:55Z 2016-02-01 1932-6203 (Online) http://lrc.quangbinhuni.edu.vn:8181/dspace/handle/DHQB_123456789/3841 en Public Library of Science (PLoS)
institution Trung tâm Học liệu Đại học Quảng Bình (Dspace)
collection Trung tâm Học liệu Đại học Quảng Bình (Dspace)
language English
topic The Genetic Architecture
Murine Glutathione Transferases
Glutathione S-transferase
spellingShingle The Genetic Architecture
Murine Glutathione Transferases
Glutathione S-transferase
Lu Lu
Ashutosh, K Pandey
M Trevor, Houseal
Megan, K Mulligan
The Genetic Architecture of Murine Glutathione Transferases
description Glutathione S-transferase (GST) genes play a protective role against oxidative stress and may influence disease risk and drug pharmacokinetics. In this study, massive multiscalar trait profiling across a large population of mice derived from a cross between C57BL/6J (B6) and DBA2/J (D2)—the BXD family—was combined with linkage and bioinformatic analyses to characterize mechanisms controlling GST expression and to identify downstream consequences of this variation. Similar to humans, mice show a wide range in expression of GST family members. Variation in the expression of Gsta4, Gstt2, Gstz1, Gsto1, and Mgst3 is modulated by local expression QTLs (eQTLs) in several tissues. Higher expression of Gsto1 in brain and liver of BXD strains is strongly associated (P < 0.01) with inheritance of the B6 parental allele whereas higher expression of Gsta4 and Mgst3 in brain and liver, and Gstt2 and Gstz1 in brain is strongly associated with inheritance of the D2 parental allele. Allele-specific assays confirmed that expression of Gsto1, Gsta4, and Mgst3 are modulated by sequence variants within or near each gene locus. We exploited this endogenous variation to identify coexpression networks and downstream targets in mouse and human. Through a combined systems genetics approach, we provide new insight into the biological role of naturally occurring variants in GST genes.
author Lu Lu
Ashutosh, K Pandey
M Trevor, Houseal
Megan, K Mulligan
author_facet Lu Lu
Ashutosh, K Pandey
M Trevor, Houseal
Megan, K Mulligan
author_sort Lu Lu
title The Genetic Architecture of Murine Glutathione Transferases
title_short The Genetic Architecture of Murine Glutathione Transferases
title_full The Genetic Architecture of Murine Glutathione Transferases
title_fullStr The Genetic Architecture of Murine Glutathione Transferases
title_full_unstemmed The Genetic Architecture of Murine Glutathione Transferases
title_sort genetic architecture of murine glutathione transferases
publisher Public Library of Science (PLoS)
publishDate 2018
url http://lrc.quangbinhuni.edu.vn:8181/dspace/handle/DHQB_123456789/3841
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score 9,463379