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由缺失同源结构域的Ftz多肽对果蝇胚胎进行模式化。

Patterning of the Drosophila embryo by a homeodomain-deleted Ftz polypeptide.

作者信息

Copeland J W, Nasiadka A, Dietrich B H, Krause H M

机构信息

Banting and Best Department of Medical Research, University of Toronto, Charles H. Best Institute, Ontario, Canada.

出版信息

Nature. 1996 Jan 11;379(6561):162-5. doi: 10.1038/379162a0.

Abstract

Homeodomain proteins regulate diverse developmental processes in a wide range of organisms, yet bind in vitro to DNA sequences that are remarkably similar. This has raised the fundamental question of how target gene specificity is achieved in vivo. The Drosophila fushi tarazu protein (Ftz) contains a homeodomain and is required for the formation of alternate segments. We have shown previously that a homeodomain-deleted Ftz polypeptide (Ftz delta HD), incapable of binding DNA in vitro, could regulate endogenous ftz gene expression. Here we test Ftz delta HD activities in a ftz mutant background and find that, surprisingly, Ftz delta HD can directly regulate ftz-dependent segmentation, suggesting that it can control target gene expression through interactions with other proteins. A likely candidate is the pair-rule protein Paired (Prd). Ftz delta HD bound directly to Prd in vitro and required Prd to repress wingless in vivo. These results emphasize the pivotal importance of protein-protein interactions in homeodomain protein function.

摘要

同源结构域蛋白在多种生物体中调节不同的发育过程,但在体外与非常相似的DNA序列结合。这就提出了一个基本问题,即在体内如何实现靶基因特异性。果蝇分节基因(Ftz)蛋白含有一个同源结构域,是形成交替节段所必需的。我们之前已经表明,一种缺失同源结构域的Ftz多肽(Ftz delta HD),在体外不能结合DNA,但可以调节内源性ftz基因的表达。在这里,我们在ftz突变背景下测试Ftz delta HD的活性,令人惊讶地发现,Ftz delta HD可以直接调节依赖Ftz的节段化,这表明它可以通过与其他蛋白质的相互作用来控制靶基因的表达。一个可能的候选蛋白是成对规则蛋白配对(Prd)。Ftz delta HD在体外直接与Prd结合,并且在体内需要Prd来抑制无翅基因。这些结果强调了蛋白质 - 蛋白质相互作用在同源结构域蛋白功能中的关键重要性。

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