Hülskamp M, Lukowitz W, Beermann A, Glaser G, Tautz D
Institut für Genetik und Mikrobiologie, Universität München, Federal Republic of Germany.
Genetics. 1994 Sep;138(1):125-34. doi: 10.1093/genetics/138.1.125.
hunchback (hb) is a key regulatory gene in the early segmentation gene hierarchy of Drosophila. It codes for a transcription factor of the Cys2-His2 zinc finger type and shows two separate zinc finger domains in its coding region. hb forms a morphogenetic gradient in the middle of the embryo that is required for setting the spatial boundaries of several target genes. We have analyzed the molecular lesions found in the different hb alleles and have studied the differential effects of these alleles on a number of such target genes. We find that in mutants in which the HB protein lacks a functional second finger domain, the regulation of the target genes Krüppel (Kr) and knirps (kni) is differentially affected. While this domain is required for the correct regulation of Kr, it is not necessary for the repression of kni. Furthermore, mutations affecting this domain lead to a decreased protein stability. The integration of the expression pattern of target genes was found to be distorted in a second class of mutants between the two finger domains which lead to gain of function or neomorphic phenotypes. The effects of these mutations were studied in detail and it was found that they fall into two classes, the first one interfering with the function of the maternal hb product, the second leading to a delayed segmentation. The function of the latter class appears to be linked to the secondary expression of hb in the parasegment 4 (PS4) stripe at blastoderm stage.
驼背基因(hb)是果蝇早期体节基因层级中的关键调控基因。它编码一种Cys2-His2锌指型转录因子,其编码区域有两个独立的锌指结构域。hb在胚胎中部形成一个形态发生梯度,这对于设定几个靶基因的空间边界是必需的。我们分析了不同hb等位基因中发现的分子损伤,并研究了这些等位基因对许多此类靶基因的不同影响。我们发现,在HB蛋白缺乏功能性第二指结构域的突变体中,靶基因克虏伯(Kr)和克尼普斯(kni)的调控受到不同影响。虽然这个结构域对于Kr的正确调控是必需的,但对于kni的抑制并非必需。此外,影响这个结构域的突变会导致蛋白质稳定性下降。在两类突变体中,发现靶基因的表达模式整合在两个指结构域之间发生扭曲,导致功能获得或新表型。对这些突变的影响进行了详细研究,发现它们分为两类,第一类干扰母体hb产物的功能,第二类导致体节延迟。后一类的功能似乎与原肠胚形成阶段副体节4(PS4)条纹中hb的二次表达有关。