通过睾丸组织的微阵列分析鉴定参与人类精子发生的十个新基因。

Identification of ten novel genes involved in human spermatogenesis by microarray analysis of testicular tissue.

作者信息

Lin Ying-Hung, Lin Yung-Ming, Teng Yen-Ni, Hsieh Tsui-Yu Tracy, Lin Yi-Shing, Kuo Pao-Lin

机构信息

Graduate Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

出版信息

Fertil Steril. 2006 Dec;86(6):1650-8. doi: 10.1016/j.fertnstert.2006.04.039. Epub 2006 Oct 30.

Abstract

OBJECTIVE

To identify novel genes that are down-regulated in the testicular tissue of infertile men.

DESIGN

Prospective study.

SETTING

University-based reproductive clinics and genetics laboratory.

PATIENTS

Nine patients with normal spermatogenesis, and 15 patients with maturation arrest (MA) or Sertoli cell-only syndrome (SCOS).

INTERVENTION

Testicular samples of patients with the same histology were pooled for complementary DNA (cDNA) microarray analysis.

MAIN OUTCOME MEASURE

Novel, down-regulated genes.

RESULTS

In total, 300 genes were significantly down-regulated in SCOS or MA samples, and 10 novel sterility-related genes were identified. Of the 10 novel genes, 6 genes (Hs.126780, Hs.553658, Hs.274135, Hs.268122, Hs.531701, and Hs.171130) encode proteins with predictable functional domains, and all these functional domains are believed to correlate with spermatogenesis and/or spermiogenesis. Conversely, the other 4 genes (Hs.351582, Hs.407480, Hs.552781, and Hs.355570) do not encompass known functional domains. Two genes (Hs.407480 and Hs.552781) lack mouse orthologues. Most novel genes showed a testis-specific expression pattern in both mice and humans. Reverse transcription-polymerase chain reaction (RT-PCR) showed three distinct types of developmental stage-dependent expressions of message ribonucleic acid (mRNA) for these novel genes in murine testes.

CONCLUSION

These 10 novel genes provide targets to elucidate novel pathways involved in human spermatogenesis.

摘要

目的

鉴定在不育男性睾丸组织中下调的新基因。

设计

前瞻性研究。

地点

大学附属生殖诊所和遗传学实验室。

患者

9名精子发生正常的患者,以及15名成熟停滞(MA)或唯支持细胞综合征(SCOS)患者。

干预

将具有相同组织学特征患者的睾丸样本汇集用于互补DNA(cDNA)微阵列分析。

主要观察指标

新的下调基因。

结果

总共300个基因在SCOS或MA样本中显著下调,鉴定出10个新的不育相关基因。在这10个新基因中,6个基因(Hs.126780、Hs.553658、Hs.274135、Hs.268122、Hs.531701和Hs.171130)编码具有可预测功能域的蛋白质,并且所有这些功能域都被认为与精子发生和/或精子形成相关。相反,其他4个基因(Hs.351582、Hs.407480、Hs.552781和Hs.355570)不包含已知的功能域。两个基因(Hs.407480和Hs.552781)缺乏小鼠同源物。大多数新基因在小鼠和人类中均表现出睾丸特异性表达模式。逆转录-聚合酶链反应(RT-PCR)显示这些新基因在小鼠睾丸中的信使核糖核酸(mRNA)有三种不同类型的发育阶段依赖性表达。

结论

这10个新基因为阐明人类精子发生所涉及的新途径提供了靶点。

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