Schlüter G, Celik A, Obata R, Schlicker M, Hofferbert S, Schlung A, Adham I M, Engel W
Institut für Humangenetik der Universität, Göttingen, Germany.
Mol Reprod Dev. 1996 Jan;43(1):1-6. doi: 10.1002/(SICI)1098-2795(199601)43:1<1::AID-MRD1>3.0.CO;2-W.
Structural data are presented on the protamine gene cluster (PGC) of human, mouse, rat, and bull. By restriction mapping we demonstrate that the organization of the protamine cluster is conserved throughout all four species, i.e., the genes are situated in a head to tail arrangement in the order: protamine 1-protamine 2-transition protein 2. Further, we established the nucleotide sequence of the entire human PGC (25 kb in total) and the 3' portion of the rat protamine cluster (PRM2 and TNP2 genes and intergenic region). In addition, a 1 kb fragment of the bovine and murine protamine cluster, situated between PRM2 and TNP2, was sequenced. This fragment is conserved regarding sequence, position, and orientation in all species examined, and was classified as likely coding region by gene recognition program GRAIL. Using the rat fragment as a probe in RNA blots, we detected a testis-specific signal of about 0.5 kb. Finally, we demonstrate a high density of Alu elements, both full and fragmented copies, in the human PGC and discuss their localization with respect to evolutionary and functional aspects.
本文展示了人类、小鼠、大鼠和公牛的鱼精蛋白基因簇(PGC)的结构数据。通过限制性图谱分析,我们证明了鱼精蛋白基因簇的组织在所有这四个物种中都是保守的,即基因以头对头的排列顺序位于:鱼精蛋白1 - 鱼精蛋白2 - 过渡蛋白2。此外,我们确定了整个人类PGC(总共25 kb)的核苷酸序列以及大鼠鱼精蛋白基因簇的3'部分(PRM2和TNP2基因以及基因间区域)。另外,对位于PRM2和TNP2之间的牛和小鼠鱼精蛋白基因簇的1 kb片段进行了测序。该片段在所有检测的物种中在序列、位置和方向上都是保守的,并通过基因识别程序GRAIL被归类为可能的编码区域。使用大鼠片段作为RNA印迹中的探针,我们检测到了一个约0.5 kb的睾丸特异性信号。最后,我们证明了人类PGC中存在高密度的Alu元件,包括完整和片段化的拷贝,并从进化和功能方面讨论了它们的定位。