An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease.
dc.contributor.author | Wang, Liuyang | |
dc.contributor.author | Pittman, Kelly J | |
dc.contributor.author | Barker, Jeffrey R | |
dc.contributor.author | Salinas, Raul E | |
dc.contributor.author | Stanaway, Ian B | |
dc.contributor.author | Williams, Graham D | |
dc.contributor.author | Carroll, Robert J | |
dc.contributor.author | Balmat, Tom | |
dc.contributor.author | Ingham, Andy | |
dc.contributor.author | Gopalakrishnan, Anusha M | |
dc.contributor.author | Gibbs, Kyle D | |
dc.contributor.author | Antonia, Alejandro L | |
dc.contributor.author | eMERGE Network | |
dc.contributor.author | Heitman, Joseph | |
dc.contributor.author | Lee, Soo Chan | |
dc.contributor.author | Jarvik, Gail P | |
dc.contributor.author | Denny, Joshua C | |
dc.contributor.author | Horner, Stacy M | |
dc.contributor.author | DeLong, Mark R | |
dc.contributor.author | Valdivia, Raphael H | |
dc.contributor.author | Crosslin, David R | |
dc.contributor.author | Ko, Dennis C | |
dc.date.accessioned | 2022-03-28T20:23:20Z | |
dc.date.available | 2022-03-28T20:23:20Z | |
dc.date.issued | 2018-08 | |
dc.date.updated | 2022-03-28T20:23:19Z | |
dc.description.abstract | Pathogens have been a strong driving force for natural selection. Therefore, understanding how human genetic differences impact infection-related cellular traits can mechanistically link genetic variation to disease susceptibility. Here we report the Hi-HOST Phenome Project (H2P2): a catalog of cellular genome-wide association studies (GWAS) comprising 79 infection-related phenotypes in response to 8 pathogens in 528 lymphoblastoid cell lines. Seventeen loci surpass genome-wide significance for infection-associated phenotypes ranging from pathogen replication to cytokine production. We combined H2P2 with clinical association data from patients to identify a SNP near CXCL10 as a risk factor for inflammatory bowel disease. A SNP in the transcriptional repressor ZBTB20 demonstrated pleiotropy, likely through suppression of multiple target genes, and was associated with viral hepatitis. These data are available on a web portal to facilitate interpreting human genome variation through the lens of cell biology and should serve as a rich resource for the research community. | |
dc.identifier | S1931-3128(18)30377-9 | |
dc.identifier.issn | 1931-3128 | |
dc.identifier.issn | 1934-6069 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | Cell host & microbe | |
dc.relation.isversionof | 10.1016/j.chom.2018.07.007 | |
dc.subject | eMERGE Network | |
dc.subject | Cell Line | |
dc.subject | Humans | |
dc.subject | Hepatitis, Viral, Human | |
dc.subject | Inflammatory Bowel Diseases | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Nerve Tissue Proteins | |
dc.subject | Transcription Factors | |
dc.subject | Antibodies, Monoclonal | |
dc.subject | Cytokines | |
dc.subject | Data Collection | |
dc.subject | Risk Factors | |
dc.subject | DNA Mutational Analysis | |
dc.subject | Computational Biology | |
dc.subject | DNA Replication | |
dc.subject | Phenotype | |
dc.subject | Genome, Human | |
dc.subject | Databases, Genetic | |
dc.subject | Chemokine CXCL10 | |
dc.subject | Genetic Variation | |
dc.subject | Genome-Wide Association Study | |
dc.subject | Electronic Health Records | |
dc.subject | Genetic Pleiotropy | |
dc.subject | Web Browser | |
dc.subject | Infections | |
dc.title | An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease. | |
dc.type | Journal article | |
duke.contributor.orcid | Wang, Liuyang|0000-0001-9556-2361 | |
duke.contributor.orcid | Salinas, Raul E|0000-0001-9011-683X | |
duke.contributor.orcid | Horner, Stacy M|0000-0002-9351-7409 | |
duke.contributor.orcid | DeLong, Mark R|0000-0003-0923-8069 | |
duke.contributor.orcid | Valdivia, Raphael H|0000-0003-0961-073X | |
duke.contributor.orcid | Ko, Dennis C|0000-0002-0113-5981 | |
pubs.begin-page | 308 | |
pubs.end-page | 323.e6 | |
pubs.issue | 2 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Faculty | |
pubs.organisational-group | Staff | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Biochemistry | |
pubs.organisational-group | Molecular Genetics and Microbiology | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Infectious Diseases | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Initiatives | |
pubs.organisational-group | Duke Science & Society | |
pubs.publication-status | Published | |
pubs.volume | 24 |
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- Name:
- Liuyang Wang, ... Raul E. Salinas, et al, 2018. Cell Host Microbe, 24(2) 308–323.pdf
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