Klein-Hessling S, Schneider G, Heinfling A, Chuvpilo S, Serfling E
Department of Molecular Pathology, University of Würzburg, Germany.
Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15311-6. doi: 10.1073/pnas.93.26.15311.
HMG I(Y) proteins bind to double-stranded A + T oligonucleotides longer than three base pairs. Such motifs form part of numerous NF-AT-binding sites of lymphokine promoters, including the interleukin 4 (IL-4) promoter. NF-AT factors share short homologous peptide sequences in their DNA-binding domain with NF-kappa B factors and bind to certain NF-kappa B sites. It has been shown that HMG I(Y) proteins enhance NF-kappa B binding to the interferon beta promoter and virus-mediated interferon beta promoter induction. We show that HMG I(Y) proteins exert an opposite effect on the DNA binding of NF-AT factors and the induction of the IL-4 promoter in T lymphocytes. Introduction of mutations into a high-affinity HMG I(Y)-binding site of the IL-4 promoter, which decreased HMG I(Y)-binding to a NF-AT-binding sequence, the Pu-bB (or P) site, distinctly increased the induction of the IL-4 promoter in Jurkat T leukemia cells. High concentrations of HMG I(Y) proteins are able to displace NF-ATp from its binding to the Pu-bB site. High HMG I(Y) concentrations are typical for Jurkat cells and peripheral blood T lymphocytes, whereas E14 T lymphoma cells and certain T helper type 2 cell clones contain relatively low HMG I(Y) concentrations. Our results indicate that HMG I(Y) proteins do not cooperate, but instead compete with NF-AT factors for the binding to DNA even though NF-AT factors share some DNA-binding to DNA even though NF-AT factors share some DNA-binding properties with NF-kB factors. This competition between HMG I(Y) and NF-AT proteins for DNA binding might be due to common contacts with minor groove nucleotides of DNA and may be one mechanism contributing to the selective IL-4 expression in certain T lymphocyte populations, such as T helper type 2 cells.
HMG I(Y)蛋白可与长度超过三个碱基对的双链A + T寡核苷酸结合。这类基序构成了包括白细胞介素4(IL-4)启动子在内的众多淋巴因子启动子的NF-AT结合位点的一部分。NF-AT因子在其DNA结合结构域中与NF-κB因子共享短的同源肽序列,并与某些NF-κB位点结合。研究表明,HMG I(Y)蛋白可增强NF-κB与干扰素β启动子的结合以及病毒介导的干扰素β启动子诱导。我们发现,HMG I(Y)蛋白对T淋巴细胞中NF-AT因子的DNA结合及IL-4启动子的诱导具有相反的作用。在IL-4启动子的一个高亲和力HMG I(Y)结合位点引入突变,该突变降低了HMG I(Y)与NF-AT结合序列Pu-bB(或P)位点的结合,显著增加了Jurkat T白血病细胞中IL-4启动子的诱导。高浓度的HMG I(Y)蛋白能够使NF-ATp从其与Pu-bB位点的结合中解离出来。Jurkat细胞和外周血T淋巴细胞中HMG I(Y)蛋白浓度较高,而E14 T淋巴瘤细胞和某些2型辅助性T细胞克隆中HMG I(Y)蛋白浓度相对较低。我们的结果表明,HMG I(Y)蛋白并不与NF-AT因子协同作用,而是与它们竞争DNA结合,尽管NF-AT因子与NF-κB因子具有一些共同的DNA结合特性。HMG I(Y)和NF-AT蛋白之间这种对DNA结合的竞争可能是由于与DNA小沟核苷酸的共同接触,并且可能是导致某些T淋巴细胞群体(如2型辅助性T细胞)中IL-4选择性表达的一种机制。