Rao V N, Reddy E S
Department of Microbiology and Immunology, Jefferson Cancer Institute, Philadelphia, Pennsylvania 19107-5541.
Cancer Res. 1993 Jan 15;53(2):215-20.
The ets oncogene superfamily codes for a family of transcriptional factors that are involved in gene regulation not only by autonomous DNA binding but also by indirect DNA binding through interaction with cellular factors. We have previously shown that a member of this superfamily, elk-1, is a sequence specific transcriptional activator, which forms a serum response factor (SRF) dependent ternary complex with serum response element (SRE) similar to p62TCF. We describe here an alternatively spliced variant of elk-1 named delta elk-1, which has lost the SRF interaction domain, negative regulatory DNA binding domain, and part of the elk-1 DNA binding domain. This variant elk-1 protein has lost the capacity to form a SRF dependent ternary complex with SRE and to activate fos transcription. Since this splice variant lacks part of the ets DNA binding domain, it binds to DNA with a specificity that is different from that of the full length elk-1 protein. Therefore differential splicing within the DNA binding and protein-protein interaction domains of transcriptional factors can generate proteins with modulated DNA binding specificities and transcriptional regulation. Thus it is conceivable that variant elk-1 might function by competing for some of the elk-1 target sequences (like SRE) and thereby block the transcriptional activation of fos by SRF and elk-1. Alternately, variant elk-1 protein may be the repressor, recruited by the SRE bound SRF for c-fos repression, or it may have an altogether different function. Therefore, elk-1 appears to fall in the category of genes that encode activators and repressors through the mechanism of differential splicing.
ets癌基因超家族编码一类转录因子,它们不仅通过自主结合DNA参与基因调控,还通过与细胞因子相互作用间接结合DNA来调控基因。我们之前已经表明,这个超家族的一个成员elk-1是一种序列特异性转录激活因子,它与血清反应元件(SRE)形成类似于p62TCF的血清反应因子(SRF)依赖性三元复合物。我们在此描述了一种名为δ elk-1的elk-1可变剪接变体,它失去了SRF相互作用结构域、负调控DNA结合结构域以及部分elk-1 DNA结合结构域。这种变体elk-1蛋白失去了与SRE形成SRF依赖性三元复合物以及激活fos转录的能力。由于这种剪接变体缺少部分ets DNA结合结构域,它与DNA结合的特异性不同于全长elk-1蛋白。因此,转录因子的DNA结合和蛋白质-蛋白质相互作用结构域内的差异剪接可以产生具有不同DNA结合特异性和转录调控的蛋白质。由此可以推测,变体elk-1可能通过竞争一些elk-1靶序列(如SRE)来发挥作用,从而阻断SRF和elk-1对fos的转录激活。或者,变体elk-1蛋白可能是由与SRE结合的SRF招募来抑制c-fos的阻遏物,或者它可能具有完全不同的功能。因此,elk-1似乎属于通过差异剪接机制编码激活因子和阻遏物的基因类别。