| Literature DB >> 19685047 |
Daniel P Potaczek1, Keiko Maeda, Qing-Hui Wang, Nobuhiro Nakano, Shunsuke Kanada, Ewa Stepien, Agnieszka Branicka, Tatsuo Fukai, Mutsuko Hara, Tomoko Tokura, Hideoki Ogawa, Anetta Undas, Ko Okumura, Chiharu Nishiyama.
Abstract
Three frequent genetic polymorphisms in the human high-affinity IgE receptor alpha-subunit (FcepsilonRIalpha) were shown to be associated with allergic disorders and/or total serum IgE levels in allergic patients. Two of these were previously demonstrated to affect FcepsilonRIalpha expression while the third -18483A>C (rs2494262) has not yet been subjected to functional studies. We hypothesized that the -18483A>C variant affects transcriptional activity of the FcepsilonRIalpha distal promoter in monocytes in which FcepsilonRIalpha transcription is driven through that regulatory region. Indeed, we confirmed preferential binding of the YY1 transcription factor to the -18483C allele, resulting in lower transcriptional activity when compared with the -18483A allele.Entities:
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Year: 2009 PMID: 19685047 DOI: 10.1007/s00251-009-0391-x
Source DB: PubMed Journal: Immunogenetics ISSN: 0093-7711 Impact factor: 2.846