Dang Duyen T, Zhao Weidong, Mahatan Channing S, Geiman Deborah E, Yang Vincent W
Division of Gastroenterology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Nucleic Acids Res. 2002 Jul 1;30(13):2736-41. doi: 10.1093/nar/gkf400.
KLF4 (Krüppel-like factor 4 or gut-enriched Krüppel-like factor, GKLF) and KLF5 (Krüppel-like factor 5 or intestinal-enriched Krüppel-like factor, IKLF) are two closely related members of the zinc finger-containing Krüppel-like factor family of transcription factors. Although both genes are expressed in the intestinal epithelium, their distributions are different: Klf4 is primarily expressed in the terminally differentiated villus cells while Klf5 is primarily in the proliferating crypt cells. Previous studies show that Klf4 is a negative regulator of cell proliferation and Klf5 is a positive regulator of cell proliferation. In this study, we demonstrate that Klf5 binds to a number of cis-DNA elements that have previously been shown to bind to Klf4. However, while Klf4 activates the promoter of its own gene, Klf5 suppresses the Klf4 promoter. Moreover, Klf5 abrogates the activating effect of Klf4 on the Klf4 promoter and Klf4 abrogates the inhibitory effect of Klf5 on the same promoter. An explanation of this competing effect is due to physical competition of the two proteins for binding to cognate DNA sequence. The complementary tissue localization of expression of Klf4 and Klf5 and the opposing effect of the two Klfs on the Klf4 promoter activity may provide a basis for the coordinated regulation of expression of the Klf4 gene in the intestinal epithelium.
KLF4(Krüppel样因子4或肠道富集型Krüppel样因子,GKLF)和KLF5(Krüppel样因子5或肠道富集型Krüppel样因子,IKLF)是含锌指的Krüppel样转录因子家族中两个密切相关的成员。尽管这两个基因均在肠上皮中表达,但其分布有所不同:Klf4主要在终末分化的绒毛细胞中表达,而Klf5主要在增殖的隐窝细胞中表达。先前的研究表明,Klf4是细胞增殖的负调节因子,而Klf5是细胞增殖的正调节因子。在本研究中,我们证明Klf5能结合许多先前已证明可与Klf4结合的顺式DNA元件。然而,虽然Klf4可激活其自身基因的启动子,但Klf5却抑制Klf4启动子。此外,Klf5可消除Klf4对Klf4启动子的激活作用,而Klf4可消除Klf5对同一启动子的抑制作用。这种竞争效应的一种解释是由于这两种蛋白质在结合同源DNA序列上存在物理竞争。Klf4和Klf5表达的互补性组织定位以及这两种Klf对Klf4启动子活性的相反作用可能为肠上皮中Klf4基因表达的协调调控提供基础。