Krawetz S A, Connor W, Dixon G H
Department of Medical Biochemistry, Faculty of Medicine, University of Calgary, Alberta, Canada.
J Biol Chem. 1988 Jan 5;263(1):321-6.
In a recent paper, we described the isolation of the first bovine protamine cDNA (BPK59), demonstrating that the gene was autosomal and single copy (Krawetz, S. A., Connor, W., and Dixon, G. H. (1987) DNA 6, 45-57). We have since utilized the BPK59 clone as a probe, to isolate both alleles of the protamine gene from a bovine genomic library constructed in Charon 28. The sequenced alleles are highly homologous and code for identical mRNAs. Unlike the trout protamine genes, the bovine gene is not contiguous as it possesses a single intron. This intron divides the highly variable mammalian carboxyl domain from the conserved protamine basic core. Three tandemly repeated CG-like ("enhancer") sequences upstream from the CAAT box have been identified, separated by a conserved spacer region. Their possible role in the transcription of this P1 gene is discussed. The bovine genome immediately surrounding (approximately equal to 20 kilobase pairs) the protamine gene has been mapped and reveals that the sequence flanking the 5' segment of the gene is unique, while the sequence flanking the 3' segment is repetitive.
在最近的一篇论文中,我们描述了首个牛精蛋白cDNA(BPK59)的分离,证明该基因是常染色体单拷贝基因(克拉韦茨,S.A.,康纳,W.,和迪克森,G.H.(1987年)《DNA》6,45 - 57)。此后,我们利用BPK59克隆作为探针,从用Charon 28构建的牛基因组文库中分离出精蛋白基因的两个等位基因。测序的等位基因高度同源,编码相同的mRNA。与鲑鱼精蛋白基因不同,牛基因并不连续,因为它有一个内含子。这个内含子将高度可变的哺乳动物羧基结构域与保守的精蛋白碱性核心分开。在CAAT框上游已鉴定出三个串联重复的CG样(“增强子”)序列,由一个保守的间隔区隔开。讨论了它们在这个P1基因转录中的可能作用。已对精蛋白基因周围(约20千碱基对)的牛基因组进行了图谱绘制,结果显示该基因5'端侧翼序列是独特的,而3'端侧翼序列是重复的。