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睾丸单倍体表达基因(THEG)的可变剪接、染色体定位及亚细胞定位

Alternative splicing, chromosome assignment and subcellular localization of the testicular haploid expressed gene (THEG).

作者信息

Mannan A, Lücke K, Dixkens C, Neesen J, Kämper M, Engel W, Burfeind P

机构信息

Institute of Human Genetics, University of Göttingen, Göttingen , Germany.

出版信息

Cytogenet Cell Genet. 2000;91(1-4):171-9. doi: 10.1159/000056840.

Abstract

We have previously isolated and characterized the mouse Testicular Haploid Expressed Gene (Theg) that is specifically expressed in haploid germ cells. We now describe the molecular cloning and characterization of the human homologue (THEG) of mouse Theg. Expression studies by using both dot blot and Northern blot techniques revealed that human THEG is expressed specifically in the testis. Additionally, we found two alternatively spliced transcripts (THEG major and THEG minor) for THEG by using reverse transcription-polymerase chain reaction on human testicular RNA. Sequence analysis of these PCR products demonstrated that the smaller transcript (THEG minor) lacks 72 bp which was also observed for the mouse Theg. We have isolated the cDNAs of human THEG major and THEG minor, containing the complete open reading frames, which encode putative nuclear proteins of 379 amino acids and 355 amino acids, respectively. Database searches identified two genomic clones on chromosome 19 harboring the human THEG gene, which is approximately 14 kb pairs in size, contains eight exons, and comparison of the two cDNA sequences with the genomic sequence indicated that the smaller transcript lacks exon 3. Furthermore, we assigned the human THEG gene (THEG) to human chromosome 19ptel--> p13 by fluorescence in situ hybridization. Moreover, we detected mouse THEG protein prominently in the nucleus of round spermatids by using an antibody against THEG on both testicular sections and cellular suspensions. Additionally, the subcellular localization of mouse THEG was confirmed by a green fluorescent protein (GFP) fusion protein of mouse THEG which was found mainly in the nucleus of transfected NIH3T3 cells. These data suggest that both human and mouse THEG are specifically expressed in the nucleus of haploid male germ cells and are involved in the regulation of nuclear functions.

摘要

我们之前已分离并鉴定了在单倍体生殖细胞中特异性表达的小鼠睾丸单倍体表达基因(Theg)。现在我们描述小鼠Theg的人类同源基因(THEG)的分子克隆和鉴定。通过斑点印迹和Northern印迹技术进行的表达研究表明,人类THEG特异性表达于睾丸中。此外,我们利用逆转录 - 聚合酶链反应对人类睾丸RNA进行研究,发现了THEG的两种选择性剪接转录本(THEG主要转录本和THEG次要转录本)。对这些PCR产物的序列分析表明,较小的转录本(THEG次要转录本)缺少72 bp,这在小鼠Theg中也有观察到。我们分离出了人类THEG主要转录本和THEG次要转录本的cDNA,它们包含完整的开放阅读框,分别编码推定的379个氨基酸和355个氨基酸的核蛋白。数据库搜索在19号染色体上鉴定出两个携带人类THEG基因的基因组克隆,该基因大小约为14 kb对,包含八个外显子,将两个cDNA序列与基因组序列进行比较表明,较小的转录本缺少外显子3。此外,我们通过荧光原位杂交将人类THEG基因(THEG)定位到人类19号染色体的ptel→p13区域。此外,我们利用针对THEG的抗体在睾丸切片和细胞悬液中均检测到小鼠THEG蛋白在圆形精子细胞的细胞核中显著存在。另外,小鼠THEG的亚细胞定位通过小鼠THEG的绿色荧光蛋白(GFP)融合蛋白得以证实,该融合蛋白主要存在于转染的NIH3T3细胞的细胞核中。这些数据表明,人类和小鼠的THEG均在单倍体雄性生殖细胞的细胞核中特异性表达,并参与核功能的调节。

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