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果蝇胚胎中Engrailed对转录抑制和激活的要求。

Requirements for transcriptional repression and activation by Engrailed in Drosophila embryos.

作者信息

Alexandre Cyrille, Vincent Jean-Paul

机构信息

National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.

出版信息

Development. 2003 Feb;130(4):729-39. doi: 10.1242/dev.00286.

DOI:10.1242/dev.00286
PMID:12506003
Abstract

Genetic analysis shows that Engrailed (En), a homeodomain-containing transcription factor, has both negative and positive targets. Negative regulation is expected from a factor that has a well-defined repressor domain but activation is harder to comprehend. We used VP16En, a form of En that had its repressor domain replaced by the activation domain of VP16, to show that En activates targets using two parallel routes, by repressing a repressor and by being a bona fide activator. We identified the intermediate repressor activity as being encoded by sloppy paired 1 and 2 and showed that bona fide activation is dramatically enhanced by Wingless signaling. Thus, En is a bifunctional transcription factor and the recruitment of additional cofactors presumably specifies which function prevails on an individual promoter. Extradenticle (Exd) is a cofactor thought to be required for activation by Hox proteins. However, in thoracic segments, Exd is required for repression (as well as activation) by En. This is consistent with in vitro results showing that Exd is involved in recognition of positive and negative targets. Moreover, we provide genetic evidence that, in abdominal segments, Ubx and Abd-A, two homeotic proteins not previously thought to participate in the segmentation cascade, are also involved in the repression of target genes by En. We suggest that, like Exd, Ubx and Abd-A could help En recognize target genes or activate the expression of factors that do so.

摘要

遗传分析表明,含同源异型结构域的转录因子“锯齿状”(En)既有负向靶标,也有正向靶标。对于一个具有明确阻遏结构域的因子来说,负向调控是可以预期的,但激活作用则较难理解。我们使用了VP16En,一种将其阻遏结构域替换为VP16激活结构域的En形式,来表明En通过抑制一个阻遏物和作为一个真正的激活物这两条平行途径激活靶标。我们确定中间阻遏活性由“配对不精确1和2”编码,并表明无翅信号通路能显著增强真正的激活作用。因此,En是一种双功能转录因子,招募额外的辅因子大概能确定在单个启动子上哪种功能占主导。额外齿(Exd)是一种被认为是Hox蛋白激活所必需的辅因子。然而,在胸节中,Exd是En进行抑制(以及激活)所必需的。这与体外实验结果一致,即Exd参与对正向和负向靶标的识别。此外,我们提供了遗传学证据,表明在腹节中,超双胸(Ubx)和腹A(Abd - A)这两种以前认为不参与体节形成级联反应的同源异型蛋白,也参与En对靶基因的抑制。我们认为,与Exd一样,Ubx和Abd - A可能有助于En识别靶基因或激活具有这种作用的因子的表达。

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