首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Transcriptome of the inner circular smooth muscle of the developing mouse intestine: Evidence for regulation of visceral smooth muscle genes by the hedgehog target gene, cJun
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Transcriptome of the inner circular smooth muscle of the developing mouse intestine: Evidence for regulation of visceral smooth muscle genes by the hedgehog target gene, cJun

机译:发育中的小鼠小肠内圆形平滑肌的转录组:刺猬靶基因cJun对内脏平滑肌基因调控的证据

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Background: Digestion is facilitated by coordinated contractions of the intestinal muscularis externa, a bilayered smooth muscle structure that is composed of inner circular muscles (ICM) and outer longitudinal muscles (OLM). We performed transcriptome analysis of intestinal mesenchyme tissue at E14.5, when the ICM, but not the OLM, is present, to investigate the transcriptional program of the ICM. Results: We identified 3967 genes enriched in E14.5 intestinal mesenchyme. The gene expression profiles were clustered and annotated to known muscle genes, identifying a muscle-enriched subcluster. Using publically available in situ data, 127 genes were verified as expressed in ICM. Examination of the promoter and regulatory regions for these co-expressed genes revealed enrichment for cJUN transcription factor binding sites, and cJUN protein was enriched in ICM. cJUN ChIP-seq, performed at E14.5, revealed that cJUN regulatory regions contain characteristics of muscle enhancers. Finally, we show that cJun is a target of Hedgehog (Hh), a signaling pathway known to be important in smooth muscle development, and identify a cJun genomic enhancer that is responsive to Hh. Conclusions: This work provides the first transcriptional catalog for the developing ICM and suggests that cJun regulates gene expression in the ICM downstream of Hh signaling. (C) 2016 Wiley Periodicals, Inc.
机译:背景:肠道外肌的协调收缩促进了消化,肠内肌是由内圆肌(ICM)和外纵肌(OLM)组成的双层平滑肌结构。当存在ICM而非OLM时,我们在E14.5处进行了肠间充质组织的转录组分析,以研究ICM的转录程序。结果:我们鉴定了3967个富含E14.5肠间质的基因。基因表达谱被聚类并标注到已知的肌肉基因上,从而鉴定出富含肌肉的亚簇。使用公开可用的原位数据,验证了127个基因在ICM中表达。对这些共表达基因的启动子和调控区的检查显示,cJUN转录因子结合位点富集,而cJUN蛋白富集在ICM中。在E14.5处进行的cJUN ChIP-seq显示,cJUN调控区含有肌肉增强剂的特征。最后,我们证明cJun是Hedgehog(Hh)的靶标,Hedgehog(Hh)是已知在平滑肌发育中很重要的信号通路,并确定了对Hh有反应的cJun基因组增强子。结论:这项工作为发展中的ICM提供了第一个转录目录,并暗示cJun调节Hh信号下游ICM中的基因表达。 (C)2016威利期刊公司

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