Benahmed Fairouz, Gross Isabelle, Gaunt Stephen J, Beck Felix, Jehan Frédéric, Domon-Dell Claire, Martin Elisabeth, Kedinger Michèle, Freund Jean-Noël, Duluc Isabelle
INSERM, U682, Strasbourg, France.
Gastroenterology. 2008 Oct;135(4):1238-1247, 1247.e1-3. doi: 10.1053/j.gastro.2008.06.045. Epub 2008 Jun 25.
BACKGROUND & AIMS: The Cdx2 homeobox gene exerts multiple functions including trophectoderm specification, antero-posterior patterning, and determination of intestinal identity. The aim of this study was to map genomic regions that regulate the transcription of Cdx2, with a particular interest in the gut.
Genomic fragments covering 13 kilobase (kb) of the mouse Cdx2 locus were analyzed in transgenic mice and in cell assays.
No fragment was active in the trophectoderm. Fragments containing the first intron and extending up to -5-kb upstream of the transcription start site became active posteriorly at gastrulation and then inactive at midgestation in every tissue including the endoderm. Specific persistence of activity in the intestinal endoderm/epithelium beyond midgestation requires extending the genomic fragment up to -9 kb. We identified a 250-base pair segment around -8.5-kb binding and responding to endodermal factors, with a stimulatory effect exerted synergistically by HNF4alpha, GATA6, Tcf4, and beta-catenin. These factors were able to activate endogenous expression of Cdx2 in nonintestinal Hela cells.
Multiple regulatory regions control the complex developmental pattern of Cdx2, including far upstream sequences required for the persistence of gene expression specifically in the gut epithelium throughout life. Cooperation between HNF4alpha, GATA6, beta-catenin, and Tcf4 contributes to the intestine-specific expression of Cdx2.
Cdx2同源盒基因具有多种功能,包括滋养外胚层特化、前后模式形成以及肠道特性的决定。本研究旨在绘制调控Cdx2转录的基因组区域,尤其关注肠道。
在转基因小鼠和细胞实验中分析了覆盖小鼠Cdx2基因座13千碱基(kb)的基因组片段。
没有片段在滋养外胚层中具有活性。包含第一个内含子并延伸至转录起始位点上游-5 kb的片段在原肠胚形成时在后部变得活跃,然后在妊娠中期在包括内胚层在内的每个组织中失活。要使肠道内胚层/上皮在妊娠中期之后仍具有特定的活性持续性,需要将基因组片段延伸至-9 kb。我们在-8.5 kb附近鉴定出一个250碱基对的片段,它能结合并响应内胚层因子,HNF4α、GATA6、Tcf4和β-连环蛋白协同发挥刺激作用。这些因子能够在非肠道的Hela细胞中激活Cdx2的内源性表达。
多个调控区域控制着Cdx2复杂的发育模式,包括在整个生命过程中肠道上皮中基因表达持续性所需的远上游序列。HNF4α、GATA6、β-连环蛋白和Tcf4之间的协同作用有助于Cdx2在肠道中的特异性表达。