CEBPG Exhibits Allele-Specific Expression in Human Bronchial Epithelial Cells
Author(s) -
Thomas Blomquist,
Ronald D. Brown,
Erin L. Crawford,
Ivana de la Serna,
Kandace J. Williams,
Youngsook Yoon,
Dawn-Alita Hernandez,
James C. Willey
Publication year - 2013
Publication title -
gene regulation and systems biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.534
H-Index - 18
ISSN - 1177-6250
DOI - 10.4137/grsb.s11879
Subject(s) - allele , genetic variation , biology , genetics , enhancer , gene , lung cancer , transcription factor , linkage disequilibrium , transcription (linguistics) , gene expression , microbiology and biotechnology , medicine , haplotype , pathology , linguistics , philosophy
Inter-individual variation in CCAAT/enhancer binding protein gamma (CEBPG) transcript expression in normal human bronchial epithelial cells (NBEC) is associated with predisposition to lung cancer. We hypothesize that this inter-individual variation is in part explained by cis-acting genetic variation in CEBPG. To test this hypothesis we measured transcript expression derived from each parental copy of CEBPG (ie, allele-specific expression; ASE). There was a significant 2.9-fold higher cell cycle-specific variation in ASE of CEBPG rs2772 A compared to C allele (P < 0.001). In 20% of NBEC samples, CEBPG rs2772 A allele was expressed on average 2.10 fold greater than rs2772 C allele. These data support the hypothesis that genetic variation in linkage disequilibrium with rs2772 influences regulation of CEBPG transcript expression through a trans-effect downstream of RNA polymerase II transcription and confirm that cis-acting genetic variation contributes to inter-individual variation in CEBPG transcript expression in NBEC, which is associated with variation in lung cancer risk.
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