Matches in SemOpenAlex for { <https://semopenalex.org/work/W2136264893> ?p ?o ?g. }
- W2136264893 endingPage "e77773" @default.
- W2136264893 startingPage "e77773" @default.
- W2136264893 abstract "DMBT is an antibacterial pattern recognition and scavenger receptor. In this study, we analyzed the role of DMBT1 single nucleotide polymorphisms (SNPs) regarding inflammatory bowel disease (IBD) susceptibility and examined their functional impact on transcription factor binding and downstream gene expression.Seven SNPs in the DMBT1 gene region were analyzed in 2073 individuals including 818 Crohn's disease (CD) patients and 972 healthy controls in two independent case-control panels. Comprehensive epistasis analyses for the known CD susceptibility genes NOD2, IL23R and IL27 were performed. The influence of IL23R variants on DMBT1 expression was analyzed. Functional analysis included siRNA transfection, quantitative PCR, western blot, electrophoretic mobility shift and luciferase assays.IL-22 induces DMBT1 protein expression in intestinal epithelial cells dependent on STAT3, ATF-2 and CREB1. IL-22 expression-modulating, CD risk-associated IL23R variants influence DMBT1 expression in CD patients and DMBT1 levels are increased in the inflamed intestinal mucosa of CD patients. Several DMBT1 SNPs were associated with CD susceptibility. SNP rs2981804 was most strongly associated with CD in the combined panel (p = 3.0 × 10(-7), OR 1.42; 95% CI 1.24-1.63). All haplotype groups tested showed highly significant associations with CD (including omnibus P-values as low as 6.1 × 10(-18)). The most strongly CD risk-associated, non-coding DMBT1 SNP rs2981804 modifies the DNA binding sites for the transcription factors CREB1 and ATF-2 and the respective genomic region comprising rs2981804 is able to act as a transcriptional regulator in vitro. Intestinal DMBT1 expression is decreased in CD patients carrying the rs2981804 CD risk allele.We identified novel associations of DMBT1 variants with CD susceptibility and discovered a novel functional role of rs2981804 in regulating DMBT1 expression. Our data suggest an important role of DMBT1 in CD pathogenesis." @default.
- W2136264893 created "2016-06-24" @default.
- W2136264893 creator A5014333518 @default.
- W2136264893 creator A5024004426 @default.
- W2136264893 creator A5025931648 @default.
- W2136264893 creator A5050433646 @default.
- W2136264893 creator A5055989419 @default.
- W2136264893 creator A5059052168 @default.
- W2136264893 creator A5073345578 @default.
- W2136264893 creator A5081904439 @default.
- W2136264893 creator A5083421637 @default.
- W2136264893 creator A5086525751 @default.
- W2136264893 date "2013-11-05" @default.
- W2136264893 modified "2023-10-18" @default.
- W2136264893 title "Intestinal DMBT1 Expression Is Modulated by Crohn’s Disease-Associated IL23R Variants and by a DMBT1 Variant Which Influences Binding of the Transcription Factors CREB1 and ATF-2" @default.
- W2136264893 cites W1492384889 @default.
- W2136264893 cites W1577872659 @default.
- W2136264893 cites W1642457845 @default.
- W2136264893 cites W1670573097 @default.
- W2136264893 cites W1854638296 @default.
- W2136264893 cites W1965425724 @default.
- W2136264893 cites W1967428712 @default.
- W2136264893 cites W1970044643 @default.
- W2136264893 cites W1980725116 @default.
- W2136264893 cites W1981714996 @default.
- W2136264893 cites W1982235565 @default.
- W2136264893 cites W1989581181 @default.
- W2136264893 cites W1990278601 @default.
- W2136264893 cites W1993243592 @default.
- W2136264893 cites W2004126676 @default.
- W2136264893 cites W2007121925 @default.
- W2136264893 cites W2011197968 @default.
- W2136264893 cites W2027560883 @default.
- W2136264893 cites W2029005330 @default.
- W2136264893 cites W2038131331 @default.
- W2136264893 cites W2042558677 @default.
- W2136264893 cites W2044921808 @default.
- W2136264893 cites W2048931632 @default.
- W2136264893 cites W2061606433 @default.
- W2136264893 cites W2065336530 @default.
- W2136264893 cites W2065442814 @default.
- W2136264893 cites W2065603426 @default.
- W2136264893 cites W2067901126 @default.
- W2136264893 cites W2075396092 @default.
- W2136264893 cites W2077903648 @default.
- W2136264893 cites W2084119784 @default.
- W2136264893 cites W2100273400 @default.
- W2136264893 cites W2100443415 @default.
- W2136264893 cites W2104201959 @default.
- W2136264893 cites W2106779017 @default.
- W2136264893 cites W2122031852 @default.
- W2136264893 cites W2123496942 @default.
- W2136264893 cites W2128498632 @default.
- W2136264893 cites W2130179794 @default.
- W2136264893 cites W2139008734 @default.
- W2136264893 cites W2140541855 @default.
- W2136264893 cites W2143625465 @default.
- W2136264893 cites W2151194840 @default.
- W2136264893 cites W2151437047 @default.
- W2136264893 cites W2151625863 @default.
- W2136264893 cites W2161771297 @default.
- W2136264893 cites W2165872127 @default.
- W2136264893 cites W2172042768 @default.
- W2136264893 cites W2188248802 @default.
- W2136264893 cites W2287321070 @default.
- W2136264893 doi "https://doi.org/10.1371/journal.pone.0077773" @default.
- W2136264893 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3818382" @default.
- W2136264893 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24223725" @default.
- W2136264893 hasPublicationYear "2013" @default.
- W2136264893 type Work @default.
- W2136264893 sameAs 2136264893 @default.
- W2136264893 citedByCount "20" @default.
- W2136264893 countsByYear W21362648932014 @default.
- W2136264893 countsByYear W21362648932015 @default.
- W2136264893 countsByYear W21362648932016 @default.
- W2136264893 countsByYear W21362648932017 @default.
- W2136264893 countsByYear W21362648932018 @default.
- W2136264893 countsByYear W21362648932020 @default.
- W2136264893 countsByYear W21362648932021 @default.
- W2136264893 countsByYear W21362648932022 @default.
- W2136264893 crossrefType "journal-article" @default.
- W2136264893 hasAuthorship W2136264893A5014333518 @default.
- W2136264893 hasAuthorship W2136264893A5024004426 @default.
- W2136264893 hasAuthorship W2136264893A5025931648 @default.
- W2136264893 hasAuthorship W2136264893A5050433646 @default.
- W2136264893 hasAuthorship W2136264893A5055989419 @default.
- W2136264893 hasAuthorship W2136264893A5059052168 @default.
- W2136264893 hasAuthorship W2136264893A5073345578 @default.
- W2136264893 hasAuthorship W2136264893A5081904439 @default.
- W2136264893 hasAuthorship W2136264893A5083421637 @default.
- W2136264893 hasAuthorship W2136264893A5086525751 @default.
- W2136264893 hasBestOaLocation W21362648931 @default.
- W2136264893 hasConcept C101762097 @default.
- W2136264893 hasConcept C104317684 @default.
- W2136264893 hasConcept C126322002 @default.
- W2136264893 hasConcept C135763542 @default.
- W2136264893 hasConcept C136449434 @default.
- W2136264893 hasConcept C139275648 @default.