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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Large Scale 7436-bp Deletions in Human Sperm Mitochondrial DNA with Spermatozoa Dysfunction and Male Infertility
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Large Scale 7436-bp Deletions in Human Sperm Mitochondrial DNA with Spermatozoa Dysfunction and Male Infertility

机译:具有精子功能障碍和男性不育的人类精子线粒体DNA中的大规模7436bp缺失

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Introduction: Mitochondria and mitochondrial DNA are essential to sperm motility and fertility. It controls growth, development and differentiation through oxidation energy supply. Mitochondrial (mtDNA) deletions or mutation are frequently attributed to defects of sperm motility and finally these deletions lead to sperm dysfunction and causes infertility in male.Aim: To investigate the correlation between large scale 7436-bp deletions in sperm mtDNA and non-motility of sperm in asthenozoospermia and Oligoasthenoteratozoospermia (OAT) infertile men.Materials and Methods: The present prospective study was carried out in Human Genetic Division, Department of Anatomy, Mahatma Gandhi Institute of Medical Sciences, Sevagram from June 2014 to July 2016. We have studied 110 asthenozoospermia and OAT infertile men whose semen profile indicated abnormal motility and 50 normal fertile controls. Of 110 infertile men, 70 had asthenozoospermia and 40 had OAT. Fractionations of spermatozoa were done in each semen sample on the basis of their motility by percoll gradients discontinuous technique. Long-range PCR was used for detection of 7436-bp deletions in sperm mtDNA and was confirmed by primer shift technique.Results: Overall eight subjects (8/110; 7.2%) of which six (6/70; 8.57%) asthenozoospermia and two (2/40; 5%) OAT had shown deletions of 7436-bp. In 40% percoll fraction had more non-motile spermatozoa than 80% percoll fraction. The non-motile spermatozoa in 40% percoll fractions showed more mtDNA deletions (7.2%) than the motile spermatozoa in 80% percoll fraction (2.7%). The sequencing of flanking regions of deleted mtDNA confirmed 7436-bp deletions. Interestingly, no deletions were found in control subjects.Conclusion: Though, the frequency of 7436-bp deletions in sperm mtDNA was low in infertile cases but meaningful indications were there when results were compared with controls. It is indicated that large scale deletions 7436-bp of mtDNA is associated with abnormal sperm motility. The 7436-bp deletions of mtDNA in spermatozoa may be one of the important causes of dysfunction and non-motile sperm.
机译:简介:线粒体和线粒体DNA对精子的活动性和生育能力至关重要。它通过氧化能量供应来控制生长,发育和分化。线粒体(mtDNA)缺失或突变通常归因于精子活动力缺陷,最终导致男性精子功能障碍并导致不育症。精子弱精子症和少精症男性不育症。材料与方法:本前瞻性研究于2014年6月至2016年7月在塞瓦格拉姆圣雄甘地医学科学研究所解剖学系人类遗传科进行。我们已研究110例弱精子症和OAT不育男性,其精液状况表明运动异常,可控制50名正常生育。在110名不育男性中,70名患有弱精子症,40名患有OAT。通过percoll梯度不连续技术在每个精液样本中根据其活力进行精子分级。远程PCR用于检测精子mtDNA中7436bp的缺失,并通过引物转移技术进行了证实。结果:总共八名受试者(8/110; 7.2%),其中六名(6/70; 8.57%)弱精子症和两个(2/40; 5%)OAT显示缺失7436-bp。在40%的percoll组分中,非运动性精子多于80%的percoll组分。 40%percoll组分中的非活动精子比80%percoll组分中的活动精子(2.7%)显示更多的mtDNA缺失(7.2%)。缺失的mtDNA侧翼区域的测序证实了7436bp的缺失。有趣的是,在对照受试者中没有发现缺失。结论:尽管,在不育病例中,精子mtDNA中7436 bp缺失的频率很低,但是当将结果与对照进行比较时,有有意义的迹象。结果表明,mtDNA的7436 bp的大规模缺失与精子运动异常有关。精子中mtDNA的7436-bp缺失可能是导致精子功能障碍和无法活动的重要原因之一。

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