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编码一种参与受精的人类精子抗原的cDNA的克隆与测序。

Cloning and sequencing of cDNA encoding for a human sperm antigen involved in fertilization.

作者信息

Zhu X, Naz R K

机构信息

Department of Obstetrics and Gynecology, Medical College of Ohio, Toledo 43614, USA.

出版信息

Mol Reprod Dev. 1998 Oct;51(2):176-83. doi: 10.1002/(SICI)1098-2795(199810)51:2<176::AID-MRD7>3.0.CO;2-N.

Abstract

A cDNA encoding for a sperm antigen, designated NZ-2, was cloned and sequenced from human testis cDNA-lambda gt11 expression library by using antibodies to human sperm surface antigens belonging to 14-18 kD molecular regions. These sperm antigens are involved in binding to zona pellucida of the human oocyte. Computer generated translation analysis of 963-bp cDNA yielded an open reading frame (ORF) of 163 amino acids (aa) with first ATG, Met start codon at nucleotide (nt) 335 and the stop codon TAA at nt 824. The NZ-2 cDNA has 335-bp 5' and 139-bp 3' noncoding regions. The translated protein has a calculated molecular weight of approximately 19 kD, and has two casein kinase II (CK-2) sites at aa 94-97 and 149-152, respectively. Extensive computer search in the GenBank, National Biomedical Research Foundation (NBRF), and Swiss database indicates it to be a novel protein, having 99.5% nt sequence similarity, except for the first 40-bp, only with the human bacterial artificial chromosome (BAC) containing cloned human sperm DNA, at position 76935-76009. The in vitro translated product of T3 RNA polymerase by using NZ-2 cDNA digested with XhoI yielded a protein band of approximately 20 kD, indicating it to be sense strand. The in vitro translated product of T7 RNA polymerase by using NZ-2 cDNA digested with NotI did not yield any protein band, indicating it to be antisense strand. The approximately 20 kD protein was recognized specifically by the antisperm IgG, not by the control IgG in the Western blot procedure. Neither antisperm IgG nor control IgG recognized any protein band in the in vitro translation products of the antisense strand. The human genomic DNAs from three different cells/tissues namely, sperm, kidney, and testis when cut by HindIII, and then hybridized with the NZ-2 cDNA probe in the Southern blot procedure, showed restriction fragment length polymorphism (RFLP). The recombinant human sperm NZ-2 antigen may find applications in the development of a contraceptive vaccine, and diagnosis and treatment of infertility in humans.

摘要

利用针对人精子表面抗原14 - 18 kD分子区域的抗体,从人睾丸cDNA - λgt11表达文库中克隆并测序了一个编码精子抗原(命名为NZ - 2)的cDNA。这些精子抗原参与与人卵母细胞透明带的结合。对963 bp cDNA进行计算机生成的翻译分析,得到一个163个氨基酸(aa)的开放阅读框(ORF),起始密码子ATG(Met)位于核苷酸(nt)335处,终止密码子TAA位于nt 824处。NZ - 2 cDNA具有335 bp的5'非编码区和139 bp的3'非编码区。翻译后的蛋白质计算分子量约为19 kD,分别在第94 - 97位氨基酸和第149 - 152位氨基酸处有两个酪蛋白激酶II(CK - 2)位点。在GenBank、国家生物医学研究基金会(NBRF)和瑞士数据库中进行广泛的计算机搜索表明,它是一种新蛋白,除了前40 bp外,与位于76935 - 76009位置的含有克隆人精子DNA的人细菌人工染色体(BAC)具有99.5%的核苷酸序列相似性。用XhoI消化的NZ - 2 cDNA通过T3 RNA聚合酶进行体外翻译,产生了一条约20 kD的蛋白带,表明它是有义链。用NotI消化的NZ - 2 cDNA通过T7 RNA聚合酶进行体外翻译,未产生任何蛋白带,表明它是反义链。在蛋白质印迹实验中,约20 kD的蛋白能被抗精子IgG特异性识别,而不能被对照IgG识别。反义链的体外翻译产物中,抗精子IgG和对照IgG均未识别出任何蛋白带。在Southern印迹实验中,来自精子、肾脏和睾丸这三种不同细胞/组织的人基因组DNA经HindIII切割后,与NZ - 2 cDNA探针杂交,显示出限制性片段长度多态性(RFLP)。重组人精子NZ - 2抗原可能在避孕疫苗的开发以及人类不孕症的诊断和治疗中得到应用。

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