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生长板区特异性调控蛋白聚糖 1 启动子的进化保守性:L-Sox5/Sox6 和 Nfi 因子结合于 TATA 附近,精细调节 Sox9 的激活。

Evolutionarily conserved, growth plate zone-specific regulation of the matrilin-1 promoter: L-Sox5/Sox6 and Nfi factors bound near TATA finely tune activation by Sox9.

机构信息

Institute of Biochemistry, Biological Research Center of the Hungarian Academy of Sciences, Szeged, Hungary.

出版信息

Mol Cell Biol. 2011 Feb;31(4):686-99. doi: 10.1128/MCB.00019-10. Epub 2010 Dec 20.

Abstract

To help uncover the mechanisms underlying the staggered expression of cartilage-specific genes in the growth plate, we dissected the transcriptional mechanisms driving expression of the matrilin-1 gene (Matn1). We show that a unique assembly of evolutionarily conserved cis-acting elements in the Matn1 proximal promoter restricts expression to the proliferative and prehypertrophic zones of the growth plate. These elements functionally interact with distal elements and likewise are capable of restricting the domain of activity of a pancartilaginous Col2a1 enhancer. The proximal elements include a Pe1 element binding the chondrogenic L-Sox5, Sox6, and Sox9 proteins, a SI element binding Nfi proteins, and an initiator Ine element binding the Sox trio and other factors. Sox9 binding to Pe1 is indispensable for functional interaction with the distal promoter. Binding of L-Sox5/Sox6 to Ine and Nfib to SI modulates Sox9 transactivation in a protein dose-dependent manner, possibly to enhance Sox9 activity in early stages of chondrogenesis and repress it at later stages. Hence, our data suggest a novel model whereby Sox and Nfi proteins bind to conserved Matn1 proximal elements and functionally interact with each other to finely tune gene expression in specific zones of the cartilage growth plate.

摘要

为了帮助揭示生长板中软骨特异性基因表达的交错机制,我们对软骨基质蛋白 1 基因(Matn1)的转录机制进行了剖析。研究表明,Matn1 近端启动子中独特的进化保守顺式作用元件组合将其表达限制在生长板的增殖和预肥大区。这些元件与远端元件具有功能相互作用,同样能够限制泛软骨性 Col2a1 增强子的活性域。近端元件包括结合软骨形成 L-Sox5、Sox6 和 Sox9 蛋白的 Pe1 元件、结合 Nfi 蛋白的 SI 元件以及结合 Sox 三蛋白和其他因子的起始 Ine 元件。Sox9 与 Pe1 的结合对于与远端启动子的功能相互作用是不可或缺的。L-Sox5/Sox6 与 Ine 的结合以及 Nfib 与 SI 的结合以蛋白剂量依赖的方式调节 Sox9 的转录激活,可能在软骨发生的早期增强 Sox9 的活性,并在后期抑制它。因此,我们的数据表明了一种新的模型,即 Sox 和 Nfi 蛋白结合到保守的 Matn1 近端元件上,并相互作用,以精细调节软骨生长板特定区域的基因表达。

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