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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Temporal ChIP-on-chip reveals Biniou as a universal regulator of the visceral muscle transcriptional network.
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Temporal ChIP-on-chip reveals Biniou as a universal regulator of the visceral muscle transcriptional network.

机译:时间片上芯片显示Biniou是内脏肌肉转录网络的通用调节剂。

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摘要

Smooth muscle plays a prominent role in many fundamental processes and diseases, yet our understanding of the transcriptional network regulating its development is very limited. The FoxF transcription factors are essential for visceral smooth muscle development in diverse species, although their direct regulatory role remains elusive. We present a transcriptional map of Biniou (a FoxF transcription factor) and Bagpipe (an Nkx factor) activity, as a first step to deciphering the developmental program regulating Drosophila visceral muscle development. A time course of chromatin immunoprecipitatation followed by microarray analysis (ChIP-on-chip) experiments and expression profiling of mutant embryos reveal a dynamic map of in vivo bound enhancers and direct target genes. While Biniou is broadly expressed, it regulates enhancers driving temporally and spatially restricted expression. In vivo reporter assays indicate that the timing of Biniou binding is a key trigger for the time span of enhancer activity.Although bagpipe and biniou mutants phenocopy each other, their regulatory potential is quite different. This network architecture was not apparent from genetic studies, and highlights Biniou as a universal regulator in all visceral muscle, regardless of its developmental origin or subsequent function. The regulatory connection of a number of Biniou target genes is conserved in mice, suggesting an ancient wiring of this developmental program.
机译:平滑肌在许多基本过程和疾病中起着重要作用,但是我们对调节其发育的转录网络的了解非常有限。 FoxF转录因子对于多种物种的内脏平滑肌发育至关重要,尽管它们的直接调节作用仍然难以捉摸。我们提供Biniou(FoxF转录因子)和Bagpipe(Nkx因子)活性的转录图,作为解密调节果蝇内脏肌肉发育的程序的第一步。染色质免疫沉淀的时间过程,然后进行微阵列分析(芯片上芯片)实验和突变胚胎的表达谱分析,揭示了体内结合的增强子和直接靶基因的动态图。虽然Biniou被广泛表达,但它调节增强子驱动时间和空间受限的表达。体内报告基因检测表明,Biniou结合的时机是增强子活性时间跨度的关键触发因素。尽管风笛和Biniou突变体在表型上相互关联,但它们的调控潜力却大不相同。从遗传学研究来看,这种网络结构尚不明显,并突显了Biniou作为所有内脏肌的通用调节剂,无论其发育起源或后续功能如何。许多Biniou目标基因的调控联系在小鼠中是保守的,这暗示了这一发展计划的古老线索。

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