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Identification of microRNAs predominately derived from testis and epididymis in human seminal plasma

机译:在人类精浆中主要来源于睾丸和附睾的微小RNA的鉴定

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Objectives: Aiming to develop potential noninvasive biomarkers for male infertility, the present study is designed to identify cell-free seminal piRNAs (PIWI-interacting RNA), and microRNAs predominately derived from testis and epididymis in human semen, which is secreted from the male accessory reproductive organs.Design and methods: The ejaculate of successfully vasectomized men does not contain any secretion from the testis or epididymis. We screened cell-free seminal piRNAs, and microRNAs that predominately derived from testis/epididymis by comparing Solexa sequencing of seminal RNA of normozoospermic donors and vasectomized men, followed by quantitative PCR validation in individuals.Results: Totally 84 seminal microRNAs exhibited levels >4-fold higher in normozoospermic donors than in vasectomized men. Subsequent quantitative PCR validation in individuals confirmed 61 microRNAs predominately secreted from testis/epididymis. Of these miRNAs, the lowest level in normozoospermic donors is >2-fold (24 miRNAs) or 0-2-fold (37 miRNAs) more than the highest level in vasectomized men. Interestingly, 28 microRNAs, which contain 5 microRNA clusters (18 microRNAs), reside on the X-chromosome. Some microRNAs have been shown or predicted to target important genes in spermatogenesis or sperm maturation. At least 995 seminal piRNAs were identified in normozoospermic donors while were absent in vasectomized men.Conclusions: The present study identified cell-free seminal piRNAs, and microRNAs that predominately derived from testis and epididymis. These small noncoding RNAs might be useful noninvasive epigenetic markers for human male infertility researches on revealing the etiology and physiopathological status of impaired sperm production and maturation.
机译:目的:本研究旨在开发潜在的用于男性不育的非侵入性生物标志物,旨在鉴定无细胞精浆piRNA(与PIWI相互作用的RNA)以及主要来自人精液中睾丸和附睾的microRNA,这些精子是从男性附件分泌的。设计和方法:成功输精管结扎的男人的射精不包含睾丸或附睾的任何分泌物。我们通过比较正常精子供体和输精管切除男人的精浆RNA的Solexa测序,然后对个体进行定量PCR验证,筛选了无细胞精浆piRNA和主要来源于睾丸/附睾的微RNA。结果:总共84个精浆microRNA的水平> 4正常精子捐献者比输精管切除者高出三倍。随后在个体中进行定量PCR验证,确认了61种主要从睾丸/附睾分泌的microRNA。在这些miRNA中,正常精子供体中的最低水平比输精管切开术的男性中的最高水平高2倍(24个miRNA)或0-2倍(37 miRNA)。有趣的是,包含5个microRNA簇(18个microRNA)的28个microRNA位于X染色体上。已经显示或预测了一些microRNA靶向精子发生或精子成熟中的重要基因。在正常精子捐献者中至少鉴定出995个精子piRNA,而在输精管切除术的男性中则不存在。这些小的非编码RNA可能是人类男性不育研究中有用的非侵入性表观遗传标记,用于揭示精子生产和成熟受损的病因和生理病理状况。

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