Kaneko Y, Takano S, Okumura K, Takenawa J, Higashituji H, Fukumoto M, Nakayama H, Fujita J
Department of Clinical Molecular Biology, Kyoto University Faculty of Medicine, Japan.
Biochem Biophys Res Commun. 1993 Dec 15;197(2):625-31. doi: 10.1006/bbrc.1993.2525.
We cloned five cDNAs encoding putative protein tyrosine phosphatases (PTPs; protein-tyrosine-phosphatase phosphohydrolase, EC 3.1.3.48) from the murine testis by using degenerate primers and the polymerase chain reaction cloning technique. Two of them were identical to the mouse cytoplasmic PTP and PTP-1B. The remaining three were likely to represent the murine counterparts of human PTP delta, human PTP epsilon, and rat striatum-enriched PTP. The cells expressing these genes were determined either by in situ hybridization histochemistry or by Northern blot hybridization. Moreover, Northern blot hybridization revealed that the transcripts of PTP-1B, mouse cytoplasmic PTP and the murine homologue of human PTP delta were quantitatively and/or structurally regulated during germ cell development, suggesting their roles in spermatogenesis.
我们使用简并引物和聚合酶链反应克隆技术,从小鼠睾丸中克隆出了五个编码假定蛋白酪氨酸磷酸酶(PTPs;蛋白酪氨酸磷酸酶磷酸水解酶,EC 3.1.3.48)的cDNA。其中两个与小鼠细胞质PTP和PTP-1B相同。其余三个可能代表人类PTPδ、人类PTPε和大鼠纹状体富集PTP的小鼠对应物。通过原位杂交组织化学或Northern印迹杂交确定表达这些基因的细胞。此外,Northern印迹杂交显示,PTP-1B、小鼠细胞质PTP和人类PTPδ的小鼠同源物的转录本在生殖细胞发育过程中受到定量和/或结构调控,表明它们在精子发生中发挥作用。