Wallace A M, Dass B, Ravnik S E, Tonk V, Jenkins N A, Gilbert D J, Copeland N G, MacDonald C C
Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Proc Natl Acad Sci U S A. 1999 Jun 8;96(12):6763-8. doi: 10.1073/pnas.96.12.6763.
Polyadenylation in male germ cells differs from that in somatic cells. Many germ cell mRNAs do not contain the canonical AAUAAA in their 3' ends but are efficiently polyadenylated. To determine whether the 64,000 Mr protein of the cleavage stimulation factor (CstF-64) is altered in male germ cells, we examined its expression in mouse testis. In addition to the 64,000 Mr form, we found a related approximately 70,000 Mr protein that is abundant in testis, at low levels in brain, and undetectable in all other tissues examined. Expression of the approximately 70,000 Mr CstF-64 was limited to meiotic spermatocytes and postmeiotic spermatids in testis. In contrast, the 64,000 Mr form was absent from spermatocytes, suggesting that the testis-specific CstF-64 might control expression of meiosis-specific genes. To determine why the 64,000 Mr CstF-64 is not expressed in spermatocytes, we mapped its chromosomal location to the X chromosome in both mouse and human. CstF-64 may, therefore, be absent in spermatocytes because the X chromosome is inactivated during male meiosis. By extension, the testis-specific CstF-64 may be expressed from an autosomal homolog of the X chromosomal gene.
雄性生殖细胞中的聚腺苷酸化与体细胞中的不同。许多生殖细胞mRNA在其3'末端不包含典型的AAUAAA,但能有效地进行聚腺苷酸化。为了确定切割刺激因子(CstF-64)的64,000 Mr蛋白在雄性生殖细胞中是否发生改变,我们检测了它在小鼠睾丸中的表达。除了64,000 Mr的形式外,我们还发现了一种相关的约70,000 Mr的蛋白,它在睾丸中含量丰富,在脑中含量较低,在所有其他检测的组织中均未检测到。约70,000 Mr的CstF-64的表达仅限于睾丸中的减数分裂精母细胞和减数分裂后精子细胞。相比之下,精母细胞中不存在64,000 Mr的形式,这表明睾丸特异性的CstF-64可能控制减数分裂特异性基因的表达。为了确定为什么64,000 Mr的CstF-64在精母细胞中不表达,我们将其染色体定位在小鼠和人类的X染色体上。因此,精母细胞中可能不存在CstF-64,因为X染色体在雄性减数分裂过程中失活。由此推断,睾丸特异性的CstF-64可能由X染色体基因的常染色体同源物表达。