Mori C, Nakamura N, Welch J E, Shiota K, Eddy E M
Department of Anatomy, Faculty of Medicine, Kyoto University, Japan.
Mol Reprod Dev. 1996 May;44(1):14-22. doi: 10.1002/(SICI)1098-2795(199605)44:1<14::AID-MRD2>3.0.CO;2-W.
Several enzymes in the glycolytic pathway are reported to have spermatogenic cell-specific isozymes. We reported recently the cloning of cDNAs representing three unique type 1 hexokinase mRNAs (mHk1-sa, mHk1-sb, and mHk1-sc) present only in mouse spermatogenic cells and the patterns of expression of these mRNAs (Mori et al., 1993: Biol Reprod 49:191-203). The mRNAs contain a spermatogenic cell-specific sequence, but lack the sequence for the porin-binding domain that somatic cell hexokinases use to bind to a pore-forming protein in the outer mitochondrial membrane. We now report the cloning of cDNAs representing three unique human type 1 hexokinase mRNAs (hHK1-ta, hHK1-tb, and hHK1-tc) expressed in testis, but not detected by Northern analysis in other human tissues. These mRNAs also contain a testis-specific sequence not present in somatic cell type 1 hexokinase, but lack the sequence for the porin-binding domain. The hHK1-tb and hHK1-tc mRNAs each contain an additional unique sequence. The testis-specific sequence of the human mRNAs is similar to the spermatogenic cell-specific sequence of the mouse mRNAs. Furthermore, Northern analysis of RNA from mouse, hamster, guinea pig, rabbit, ram, human, and rat demonstrated expression of type 1 hexokinase mRNAs lacking the porin-binding domain in the testes of these mammals. These results suggest that hexokinase may have unique structural or functional features in spermatogenic cells and support a model proposed by others for hexokinase gene evolution in mammals.
据报道,糖酵解途径中的几种酶具有生精细胞特异性同工酶。我们最近报道了代表三种仅存在于小鼠生精细胞中的独特1型己糖激酶mRNA(mHk1-sa、mHk1-sb和mHk1-sc)的cDNA克隆以及这些mRNA的表达模式(Mori等人,1993年:《生物繁殖》49:191 - 203)。这些mRNA包含生精细胞特异性序列,但缺乏体细胞己糖激酶用于结合线粒体外膜中孔形成蛋白的孔蛋白结合域序列。我们现在报道代表三种在睾丸中表达但在其他人类组织的Northern分析中未检测到的独特人类1型己糖激酶mRNA(hHK1-ta、hHK1-tb和hHK1-tc)的cDNA克隆。这些mRNA也包含体细胞1型己糖激酶中不存在的睾丸特异性序列,但缺乏孔蛋白结合域序列。hHK1-tb和hHK1-tc mRNA各自还包含一个额外的独特序列。人类mRNA的睾丸特异性序列与小鼠mRNA的生精细胞特异性序列相似。此外,对来自小鼠、仓鼠、豚鼠、兔子、公羊、人类和大鼠的RNA进行的Northern分析表明,这些哺乳动物的睾丸中存在缺乏孔蛋白结合域的1型己糖激酶mRNA表达。这些结果表明,己糖激酶在生精细胞中可能具有独特的结构或功能特征,并支持其他人提出的哺乳动物己糖激酶基因进化模型。