Suppr超能文献

一个进化上保守的增强子调控了发育中门牙和肢芽中 Bmp4 的表达。

An evolutionarily conserved enhancer regulates Bmp4 expression in developing incisor and limb bud.

机构信息

Division of Genetics, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Boston Massachusetts, United States of America.

出版信息

PLoS One. 2012;7(6):e38568. doi: 10.1371/journal.pone.0038568. Epub 2012 Jun 12.

Abstract

To elucidate the transcriptional regulation of Bmp4 expression during organogenesis, we used phylogenetic footprinting and transgenic reporter analyses to identify Bmp4 cis-regulatory modules (CRMs). These analyses identified a regulatory region located ∼46 kb upstream of the mouse Bmp4 transcription start site that had previously been shown to direct expression in lateral plate mesoderm. We refined this regulatory region to a 396-bp minimal enhancer, and show that it recapitulates features of endogenous Bmp4 expression in developing mandibular arch ectoderm and incisor epithelium during the initiation-stage of tooth development. In addition, this enhancer directs expression in the apical ectodermal ridge (AER) of the developing limb and in anterior and posterior limb mesenchyme. Transcript profiling of E11.5 mouse incisor dental lamina, together with protein binding microarray (PBM) analyses, allowed identification of a conserved DNA binding motif in the Bmp4 enhancer for Pitx homeoproteins, which are also expressed in the developing mandibular and incisor epithelium. In vitro electrophoretic mobility shift assays (EMSA) and in vivo transgenic reporter mutational analyses revealed that this site supports Pitx binding and that the site is necessary to recapitulate aspects of endogenous Bmp4 expression in developing craniofacial and limb tissues. Finally, Pitx2 chromatin immunoprecipitation (ChIP) demonstrated direct binding of Pitx2 to this Bmp4 enhancer site in a dental epithelial cell line. These results establish a direct molecular regulatory link between Pitx family members and Bmp4 gene expression in developing incisor epithelium.

摘要

为了阐明器官发生过程中 Bmp4 表达的转录调控,我们使用系统发育足迹分析和转基因报告基因分析来鉴定 Bmp4 顺式调控模块(CRMs)。这些分析确定了一个位于小鼠 Bmp4 转录起始位点上游约 46kb 的调控区域,该区域先前已被证明可指导侧板中胚层的表达。我们将这个调控区域精确定位到一个 396bp 的最小增强子上,并证明它在牙齿发育起始阶段中,可重现内源性 Bmp4 在发育中的下颌弓外胚层和切牙上皮中的表达特征。此外,这个增强子可指导发育中的肢端顶外胚层嵴(AER)和肢端前后中胚层的表达。E11.5 天小鼠切牙牙蕾的转录谱分析,加上蛋白质结合微阵列(PBM)分析,鉴定出了 Bmp4 增强子中用于 Pitx 同源蛋白的保守 DNA 结合基序,Pitx 同源蛋白也在发育中的下颌和切牙上皮中表达。体外电泳迁移率变动分析(EMSA)和体内转基因报告基因突变分析表明,该位点支持 Pitx 结合,并且该位点对于重现内源性 Bmp4 在发育中的颅面和肢组织中的表达特征是必需的。最后,Pitx2 染色质免疫沉淀(ChIP)实验表明,Pitx2 直接结合到这个 Bmp4 增强子位点上,该实验是在一个牙上皮细胞系中进行的。这些结果确立了 Pitx 家族成员与发育中的切牙上皮中 Bmp4 基因表达之间的直接分子调控联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9be/3373496/6cb00c23f2a5/pone.0038568.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验