Lemaire P, Vesque C, Schmitt J, Stunnenberg H, Frank R, Charnay P
Laboratoire de Génétique Moléculaire, Centre National de la Recherche Scientifique D 1302, Ecole Normale Supérieure, Paris, France.
Mol Cell Biol. 1990 Jul;10(7):3456-67. doi: 10.1128/mcb.10.7.3456-3467.1990.
The mouse gene Krox-24 is transiently activated during cell cycle reentry. It encodes a protein with three zinc fingers similar to those of the transcription factor Sp1. Here we present a biochemical characterization of the gene products. Krox-24 mRNA is translated into two proteins of 82 and 88 kilodaltons, designated p82Krox-24 and p88Krox-24, respectively. p82Krox-24 is initiated at the first AUG codon of the open reading frame, whereas synthesis of p88Krox-24 starts at a non-AUG codon located upstream. Both proteins were synthesized in HeLa cells infected with recombinant vaccinia viruses expressing Krox-24 cDNAs. Under these conditions, they were found phosphorylated on serine residues and glycosylated. The availability of the proteins made possible the determination of the DNA recognition sequence. In vitro, Krox-24 bound specifically to the sequence 5'-GCG(C/G)GGGCG-3'. This sequence is similar but not identical to the Sp1 target sequence. Insertion of an oligomer for the binding site in cis, close to the herpes simplex virus thymidine kinase promoter, rendered this promoter responsive to Krox-24. Krox-24 is therefore a sequence-specific transcriptional activator. Krox-24-binding sites were found upstream of several serum-inducible genes, raising the possibility that Krox-24 is involved in the regulation of these genes.
小鼠基因Krox - 24在细胞周期重新进入过程中被短暂激活。它编码一种具有三个锌指结构的蛋白质,与转录因子Sp1的锌指结构相似。在此,我们对该基因产物进行了生化特性分析。Krox - 24 mRNA翻译产生两种蛋白质,分子量分别为82千道尔顿和88千道尔顿,分别命名为p82Krox - 24和p88Krox - 24。p82Krox - 24从开放阅读框的第一个AUG密码子起始翻译,而p88Krox - 24的合成则起始于位于上游的一个非AUG密码子。这两种蛋白质均在感染了表达Krox - 24 cDNA的重组痘苗病毒的HeLa细胞中合成。在这些条件下,发现它们在丝氨酸残基上发生了磷酸化且进行了糖基化。这些蛋白质的可获得性使得确定DNA识别序列成为可能。在体外,Krox - 24特异性结合序列5'-GCG(C/G)GGGCG - 3'。该序列与Sp1靶序列相似但并不相同。在单纯疱疹病毒胸苷激酶启动子附近顺式插入一个用于结合位点的寡聚物,可使该启动子对Krox - 24产生反应。因此,Krox - 24是一种序列特异性转录激活因子。在几个血清诱导基因的上游发现了Krox - 24结合位点,这增加了Krox - 24参与这些基因调控的可能性。