Zappavigna V, Renucci A, Izpisúa-Belmonte J C, Urier G, Peschle C, Duboule D
EMBL, Heidelberg, FRG.
EMBO J. 1991 Dec;10(13):4177-87. doi: 10.1002/j.1460-2075.1991.tb04996.x.
We have looked for the binding of several HOX4 complex homeoproteins in the genomic region containing the HOX4C promoter, between the human HOX4C and HOX4D genes. The HOX4C, HOX4D and Hox-4.3 homeoproteins bind to a phylogenetically highly conserved DNA fragment, which is located in the proximal part of this intergenic region and contains multiple binding sites for these HOX4 proteins. Using cotransfection experiments, we show that this endogenous DNA sequence can mediate transactivation by the HOX4D and HOX4C proteins and that this effect requires the presence of TAAT-related binding sites. The Hox-4.3 protein, in contrast, is unable to activate and can repress the activation observed with the two other proteins. These results show that the HOX4D and HOX4C genes are genuine sequence-specific transcription factors and suggest that, as in Drosophila, cross-regulatory interactions between these genes might be essential for their proper expression.
我们在包含HOX4C启动子的基因组区域中,即在人类HOX4C基因和HOX4D基因之间,寻找了几种HOX4复合体同源异形蛋白的结合情况。HOX4C、HOX4D和Hox - 4.3同源异形蛋白与一个在系统发育上高度保守的DNA片段结合,该片段位于这个基因间区域的近端,并且包含这些HOX4蛋白的多个结合位点。通过共转染实验,我们表明这种内源性DNA序列可以介导HOX4D和HOX4C蛋白的反式激活作用,并且这种效应需要存在与TAAT相关的结合位点。相比之下,Hox - 4.3蛋白无法激活,并且能够抑制另外两种蛋白所观察到的激活作用。这些结果表明HOX4D和HOX4C基因是真正的序列特异性转录因子,并表明,如同在果蝇中一样,这些基因之间的交叉调控相互作用可能对它们的正常表达至关重要。