Mohr S E, Boswell R E
Howard Hughes Medical Institute, Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309-0347, USA.
Gene. 1999 Mar 18;229(1-2):109-16. doi: 10.1016/s0378-1119(99)00033-5.
The related mouse proteins Miz1 and PIAS3, which have predicted zinc finger domains, interact with the transcription factors Msx2 and STAT3, modulating the ability of Msx2 and STAT3 to regulate transcription. Here, we describe a Drosophila gene, zimp, that encodes a protein with similarity to Miz1 and PIAS3. The zimp gene appears to be post-transcriptionally regulated, as three alternatively spliced forms are detected in a cDNA library screen and on an RNA blot. In addition, all three zimp transcripts are detected in embryonic mRNA, but only two of the transcripts are detected in adult mRNA. The three transcripts have the ability to encode two proteins, of 554 and 522 amino acids. The two Zimp amino acid sequences share an amino-terminal 515-amino-acid region and differ in their carboxy-termini. These proteins and related proteins in other organisms, including mammals, C. elegans, yeast, and plants, share a highly conserved region predicted to form a zinc finger. Deletion of the zimp gene or P-element insertion in zimp is lethal; thus, zimp is an essential gene in Drosophila. These data underscore the potential importance of Zimp-related proteins cross-species, and conservation of the putative zinc finger domain suggests that it is functionally important.
相关的小鼠蛋白Miz1和PIAS3具有预测的锌指结构域,它们与转录因子Msx2和STAT3相互作用,调节Msx2和STAT3调控转录的能力。在此,我们描述了一个果蝇基因zimp,它编码一种与Miz1和PIAS3相似的蛋白质。zimp基因似乎受到转录后调控,因为在cDNA文库筛选和RNA印迹中检测到三种可变剪接形式。此外,在胚胎mRNA中检测到所有三种zimp转录本,但在成体mRNA中仅检测到其中两种转录本。这三种转录本能够编码两种蛋白质,分别为554个和522个氨基酸。这两种Zimp氨基酸序列在氨基末端有一个515个氨基酸的区域相同,而羧基末端不同。这些蛋白质以及其他生物体(包括哺乳动物、秀丽隐杆线虫、酵母和植物)中的相关蛋白质,都有一个预测会形成锌指的高度保守区域。zimp基因的缺失或zimp中的P元素插入是致死的;因此,zimp是果蝇中的一个必需基因。这些数据强调了Zimp相关蛋白在跨物种中的潜在重要性,并且假定锌指结构域的保守性表明它在功能上很重要。