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Identification and characterization of SEC24D as a susceptibility gene for hepatitis B virus infection.

Authors :
Jiang, Xianzhong
Zhang, Bin
Zhao, Junsheng
Xu, Yi
Han, Haijun
Su, Kunkai
Tao, Jingjing
Fan, Rongli
Zhao, Xinyi
Li, Lanjuan
Li, Ming D.
Source :
Scientific Reports; 9/17/2019, Vol. 9 Issue 1, pN.PAG-N.PAG, 1p
Publication Year :
2019

Abstract

Single nucleotide polymorphisms (SNPs) and genes associated with susceptibility to hepatitis B virus (HBV) infection that have been identified by genome-wide association studies explain only a limited portion of the known heritability, indicating more genetic variants remain to be discovered. In this study, we adopted a new research strategy to identify more susceptibility genes and variants for HBV infection. We first performed genetic association analysis of 300 sib-pairs and 3,087 case-control samples, which revealed that 36 SNPs located in 31 genes showed nominal associations with HBV infection in both samples. Of these genes, we selected SEC24D for further molecular analysis according to the following two main lines of evidence. First, a time course analysis of the expression profiles from HBV-infected primary human hepatocytes (PHH) demonstrated that SEC24D expression increased markedly as time passed after HBV infection (P = 4.0 × 10<superscript>−4</superscript>). Second, SNP rs76459466 in SEC24D was adversely associated with HBV risk (OR<subscript>meta</subscript> = 0.82; P<subscript>meta</subscript> = 0.002), which again indicated that SEC24D represents a novel susceptibility gene for HBV infection. Moreover, SEC24D appeared to be protective against HBV infection in vitro. Consistently, we found that SEC24D expression was significantly enhanced in non-infected liver tissues (P = 0.002). We conclude that SEC24D is a novel candidate gene linked to susceptibility to HBV infection. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20452322
Volume :
9
Issue :
1
Database :
Complementary Index
Journal :
Scientific Reports
Publication Type :
Academic Journal
Accession number :
138666707
Full Text :
https://doi.org/10.1038/s41598-019-49777-8