La Rosée-Borggreve A, Häder T, Wainwright D, Sauer F, Jäckle H
Abteilung Molekulare Entwicklungsbiologie, Max-Planck-Institut für biophysikalische Chemie, Am Fassberg, D-37077, Göttingen, Germany.
Mech Dev. 1999 Dec;89(1-2):133-40. doi: 10.1016/s0925-4773(99)00219-1.
The Drosophila gap gene Krüppel (Kr) encodes a zinc finger-type transcription factor required for controlling the spatial expression of other segmentation genes during early blastoderm stage. Here we show that two independent and transferable repressor domains of Krüppel act to control expression of the pair-rule gene hairy, and that the minimal cis-acting element of hairy stripe7 (h7) mediates either Krüppel-dependent activation or repression in different regions of the blastoderm embryo. The C-terminal region of Krüppel which encompasses the predominant repressor domain is not essential for activation, but is required to fully suppress h7-mediated transcription in response to high levels of Krüppel activity. This domain contains an interaction motif for dCtBP, a homologue of the human co-repressor CtBP. dCtBP activity is, however, dispensable for Krüppel-mediated repression in the embryo since Krüppel-mediated repression functions in the absence of dCtBP. Possible modes of h7-mediated gene regulation in response to the different domains and levels of Krüppel are discussed.
果蝇裂隙基因Krüppel(Kr)编码一种锌指型转录因子,在胚盘早期阶段控制其他体节基因的空间表达时是必需的。我们在此表明,Krüppel的两个独立且可转移的抑制结构域可控制成对规则基因hairy的表达,并且hairy条纹7(h7)的最小顺式作用元件在胚盘胚胎的不同区域介导Krüppel依赖性激活或抑制。Krüppel的C末端区域包含主要的抑制结构域,对激活不是必需的,但在高水平Krüppel活性响应时,是完全抑制h7介导的转录所必需的。该结构域包含与人共抑制因子CtBP的同源物dCtBP的相互作用基序。然而,dCtBP活性对于胚胎中Krüppel介导的抑制是可有可无的,因为Krüppel介导的抑制在没有dCtBP的情况下也能发挥作用。本文讨论了h7响应Krüppel的不同结构域和水平介导基因调控的可能模式。