van der Hoorn F A, Spiegel J E, Maylié-Pfenninger M F, Nordeen S K
Department of Medical Biochemistry, University of Calgary, Alberta, Canada.
Oncogene. 1991 Jun;6(6):929-32.
We have investigated the RNA and protein expression pattern of the rat c-mos proto-oncogene during spermatogenesis. In mouse testis a 43kD c-mos protein is expressed throughout spermatogenesis, which is in agreement with one report detecting a 1.7 kb c-mos RNA in pachytene spermatocytes and in early spermatids. However, several other reports show that the mouse 1.7 kb c-mos RNA is exclusively expressed in post-meiotic male germ cells. We report that in rat male germ cells three c-mos RNA species of 5, 3.6 and 1.7 kb are detectable by Northern blotting analysis both before and after meiosis, with highest levels in early spermatids. However, western immuno-blot analysis reveals the presence of a 43 kD c-mos protein in total testis and pachytene spermatocytes, but not in post-meiotic cells. These findings combined with those made in the mouse system strongly suggest that c-mos protein may be a regulator of meiosis during spermatogenesis.
我们研究了大鼠c-mos原癌基因在精子发生过程中的RNA和蛋白质表达模式。在小鼠睾丸中,一种43kD的c-mos蛋白在整个精子发生过程中均有表达,这与一份报告一致,该报告在粗线期精母细胞和早期精子细胞中检测到了1.7kb的c-mos RNA。然而,其他几份报告显示,小鼠1.7kb的c-mos RNA仅在减数分裂后的雄性生殖细胞中表达。我们报告称,在大鼠雄性生殖细胞中,通过Northern印迹分析在减数分裂前后均可检测到5kb、3.6kb和1.7kb的三种c-mos RNA,在早期精子细胞中水平最高。然而,蛋白质免疫印迹分析显示,在整个睾丸和粗线期精母细胞中存在43kD的c-mos蛋白,但在减数分裂后的细胞中不存在。这些发现与在小鼠系统中的发现相结合,强烈表明c-mos蛋白可能是精子发生过程中减数分裂的调节因子。