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Gene expression profiles of Bapx1 expressing {FACS} sorted cells from wildtype and Bapx1-EGFP null mouse embryos

机译:来自野生型和Bapx1-EGFP空小鼠胚胎的表达Bapx1的{FACS}分选细胞的基因表达谱

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Abstract The data described in this article refers to Chatterjee et al. (2015) “In vivo genome-wide analysis of multiple tissues identifies gene regulatory networks, novel functions and downstream regulatory genes for Bapx1 and its co-regulation with Sox9 in the mammalian vertebral column” (GEO GSE35649) [1]. Transcriptional profiling combined with genome wide binding data is a powerful tool to elucidate the molecular mechanism behind vertebrate organogenesis. It also helps to uncover multiple roles of a single gene in different organs. In the above mentioned report we reveal the function of the homeobox gene Bapx1 during the embryogenesis of five distinct organs (vertebral column, spleen, gut, forelimb and hindlimb) at a relevant developmental stage (E12.5), microarray analysis of isolated wildtype and mutant cells in is compared in conjunction with ChIP-Seq analysis. We also analyzed the development of the vertebral column by comparing microarray and ChIP-Seq data for Bapx1 with similarly generated data sets for Sox9 to generate a gene regulatory network controlling various facets of the organogenesis.
机译:摘要本文描述的数据参考Chatterjee等。 (2015年)“对多个组织的体内全基因组分析确定了Bapx1的基因调控网络,新功能和下游调控基因,以及它与哺乳动物脊柱中的Sox9共同调控”(GEO GSE35649)[1]。转录分析与全基因组结合数据相结合是阐明脊椎动物器官发生背后的分子机制的有力工具。它还有助于揭示单个基因在不同器官中的多种作用。在上述报告中,我们揭示了同源盒基因Bapx1在相关发育阶段(E12.5)的五个不同器官(椎骨,脾脏,肠道,前肢和后肢)的胚胎发生过程中的功能,分离的野生型和野生型的微阵列分析将突变细胞与ChIP-Seq分析结合进行比较。我们还通过比较Bapx1的微阵列和ChIP-Seq数据与Sox9的相似生成的数据集进行比较,分析了椎柱的发育,以生成控制器官发生各个方面的基因调控网络。

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