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c-MYC信使核糖核酸存在于人类精子细胞中。

c-MYC mRNA is present in human sperm cells.

作者信息

Kumar G, Patel D, Naz R K

机构信息

Department of Molecular Biology and Genetics, Wayne State University, Detroit, MI 48201.

出版信息

Cell Mol Biol Res. 1993;39(2):111-7.

PMID:8220581
Abstract

Stage-specific expression of proto-oncogenes, including c-myc, has been demonstrated during spermatogenesis in testis. Some of these proto-oncogenes are expressed postmeiotically, especially in the round spermatid stage. Recently, we demonstrated the presence of c-myc protein in mature ejaculated sperm cells with a possible role in sperm cell function. Since the half-life of c-myc protein has been shown to be short, we suspected the presence of c-myc mRNA in human sperm cells. In the present study, the presence of the c-myc mRNA transcript in human sperm cells was investigated by reverse transcriptase-polymerase chain reaction (RT-PCR) analysis and in situ hybridization. Total RNA, 5-10 micrograms, was extracted from 0.2-0.5 ml of pelleted human sperm cells by NP-40 lysis procedure, and was used to construct cDNA with pd(N)6 random primer and Moloney Murine Leukemia Virus (MMLV) reverse transcriptase. The PCR with sperm cDNA and primers #P1 and #P2, both from exon 3, resulted in amplification of the expected 322 bp product. Primers #P3 and #P4, which are located in exon 2 and exon 3, respectively, and are 1.37 kb apart, gave the expected PCR amplified 313 bp product ruling out the possibility of DNA contamination. The presence of c-myc mRNA in human sperm cells was further confirmed by in situ hybridization using a digoxigenin labelled DNA probe, containing exon 2 of the c-myc gene sequence. The c-myc specific DNA probe reacted with the postacrosomal mid-piece and tail regions of both noncapacitated as well as capacitated methanol-fixed sperm cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

原癌基因(包括c-myc)在睾丸精子发生过程中的阶段特异性表达已得到证实。其中一些原癌基因在减数分裂后表达,尤其是在圆形精子细胞阶段。最近,我们证明成熟射精精子细胞中存在c-myc蛋白,其可能在精子细胞功能中发挥作用。由于已表明c-myc蛋白的半衰期很短,我们推测人类精子细胞中存在c-myc mRNA。在本研究中,通过逆转录聚合酶链反应(RT-PCR)分析和原位杂交研究了人类精子细胞中c-myc mRNA转录本的存在情况。通过NP-40裂解程序从0.2-0.5 ml沉淀的人类精子细胞中提取5-10微克总RNA,并用于用pd(N)6随机引物和莫洛尼鼠白血病病毒(MMLV)逆转录酶构建cDNA。用精子cDNA和均来自外显子3的引物#P1和#P2进行PCR,扩增出预期的322 bp产物。分别位于外显子2和外显子3且相距1.37 kb的引物#P3和#P4,得到预期的PCR扩增313 bp产物,排除了DNA污染的可能性。使用含有c-myc基因序列外显子2的地高辛标记DNA探针进行原位杂交,进一步证实了人类精子细胞中存在c-myc mRNA。c-myc特异性DNA探针与未获能以及获能的甲醇固定精子细胞的顶体后中段和尾部区域发生反应。(摘要截短至250字)

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