Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Andrologia. 2014 Mar;46(2):158-66. doi: 10.1111/and.12064. Epub 2013 Jan 7.
Asthenozoospermia (AZS) is a major cause of male infertility, aetiology of which is reported to be related with gene mutation or deletion. However, studies on candidate genes for AZS are very scarce. In this study, we examined the gene expression profiles of asthenozoosperm. Gene expression profile analyses with microarray on spermatozoa specimens from 12 asthenozoosperm patients and 12 age-matched volunteers were performed; data analysis was performed with bioinformatics tools. Data analysis revealed that 1265 and 262 genes were significantly (P < 0.05) and differently expressed (≥2-fold) between groups performed with GeneSpring and BRB-ArrayTools respectively. Of these differently expressed genes, 71 were identified as molecular signatures of asthenozoosperm, of which most involved in primary metabolic process and cellular metabolic process. Molecular signatures were filtered performed with NextBio, 21 genes were identified to be specially expressed in asthenozoosperm. We used Finding Associated Concepts with Text Analysis to match the specially expressed genes against the MEDLINE database and found SEMG1 and PGAP1 were related to male fertility. Validation of the microarray data of SEMG1 was carried out using real-time PCR. Our study demonstrated that SEMG1 was significantly changed in asthenozoosperm, which could be the candidate gene for the development of diagnostic marker and provided the opportunity to further illustrate the biological mechanisms of asthenozoosperm.
弱精子症(AZS)是男性不育的主要原因,其病因据报道与基因突变或缺失有关。然而,对 AZS 的候选基因的研究非常有限。在这项研究中,我们检查了弱精子症的基因表达谱。对 12 名弱精子症患者和 12 名年龄匹配的志愿者的精子标本进行了微阵列基因表达谱分析;使用生物信息学工具进行数据分析。数据分析显示,使用 GeneSpring 和 BRB-ArrayTools 分别进行的两组之间有 1265 个和 262 个基因显著(P < 0.05)和差异表达(≥2 倍)。在这些差异表达的基因中,有 71 个被鉴定为弱精子症的分子特征,其中大多数涉及初级代谢过程和细胞代谢过程。使用 NextBio 进行分子特征筛选,鉴定出 21 个在弱精子症中特异性表达的基因。我们使用文本分析寻找关联概念,将特异性表达的基因与 MEDLINE 数据库进行匹配,发现 SEMG1 和 PGAP1 与男性生育力有关。使用实时 PCR 对 SEMG1 的微阵列数据进行验证。我们的研究表明,SEMG1 在弱精子症中发生了显著变化,它可能是诊断标志物开发的候选基因,并为进一步阐明弱精子症的生物学机制提供了机会。