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一个Hox靶基因的多因素调控

Multifactorial regulation of a hox target gene.

作者信息

Stöbe Petra, Stein M A Sokrates, Habring-Müller Anette, Bezdan Daniela, Fuchs Aurelia L, Hueber Stefanie D, Wu Haijia, Lohmann Ingrid

机构信息

Department of Molecular Biology, Max Planck Institute for Developmental Biology, Tübingen, Germany.

出版信息

PLoS Genet. 2009 Mar;5(3):e1000412. doi: 10.1371/journal.pgen.1000412. Epub 2009 Mar 13.

Abstract

Hox proteins play fundamental roles in controlling morphogenetic diversity along the anterior-posterior body axis of animals by regulating distinct sets of target genes. Within their rather broad expression domains, individual Hox proteins control cell diversification and pattern formation and consequently target gene expression in a highly localized manner, sometimes even only in a single cell. To achieve this high-regulatory specificity, it has been postulated that Hox proteins co-operate with other transcription factors to activate or repress their target genes in a highly context-specific manner in vivo. However, only a few of these factors have been identified. Here, we analyze the regulation of the cell death gene reaper (rpr) by the Hox protein Deformed (Dfd) and suggest that local activation of rpr expression in the anterior part of the maxillary segment is achieved through a combinatorial interaction of Dfd with at least eight functionally diverse transcriptional regulators on a minimal enhancer. It follows that context-dependent combinations of Hox proteins and other transcription factors on small, modular Hox response elements (HREs) could be responsible for the proper spatio-temporal expression of Hox targets. Thus, a large number of transcription factors are likely to be directly involved in Hox target gene regulation in vivo.

摘要

Hox蛋白通过调控不同的靶基因集,在控制动物前后体轴的形态发生多样性方面发挥着基本作用。在其相当广泛的表达域内,单个Hox蛋白控制细胞分化和模式形成,并因此以高度局部化的方式调控靶基因表达,有时甚至仅在单个细胞中起作用。为了实现这种高度的调控特异性,据推测Hox蛋白与其他转录因子协同作用,在体内以高度依赖上下文的方式激活或抑制其靶基因。然而,这些因子中只有少数已被鉴定出来。在这里,我们分析了Hox蛋白变形(Dfd)对细胞死亡基因收割者(rpr)的调控,并表明上颌节段前部rpr表达的局部激活是通过Dfd与最小增强子上至少八个功能多样的转录调节因子的组合相互作用实现的。由此可见,Hox蛋白和其他转录因子在小的模块化Hox反应元件(HRE)上依赖上下文的组合可能负责Hox靶标的正确时空表达。因此,大量转录因子可能直接参与体内Hox靶基因的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/2646128/e0dabb496e13/pgen.1000412.g001.jpg

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