Cannarella Rossella, Condorelli Rosita A, La Vignera Sandro, Bellucci Catia, Luca Giovanni, Calafiore Riccardo, Calogero Aldo E
Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Department of Experimental Medicine, University of Perugia, Perugia, Italy.
World J Mens Health. 2020 Oct;38(4):545-551. doi: 10.5534/wjmh.190070. Epub 2019 Aug 20.
Oligozoospermia is highly prevalent worldwide. Studies have reported a lower methylation rate in the differentially methylated region at the sperm level in oligozoospermic patients than in controls. are the best-known pair of imprinted genes. However, no studies have yet evaluated whether they are transcribed in human sperm. To assess whether and mRNAs are present in human sperm and if their levels are correlated with sperm concentration and total sperm count.
Sperm samples (n=22) underwent reverse-transcription quantitative polymerase chain reaction using specific primers to detect and mRNA levels. They were then correlated with patients' conventional sperm parameters using the Spearman (τ) and Kendall (ρ) rank correlation coefficients.
Statistically significant positive correlations were found between mRNA levels and sperm concentration (τ=0.403, p<0.01; ρ=0.587, p<0.005) and total sperm count (τ=0.347, p<0.024; ρ=0.509, p<0.015). mRNA levels were positively correlated with sperm concentration (τ=0.595, p<0.001; ρ=0.774, p<0.001) and total sperm count (τ=0.547, p<0.001; ρ=0.701, p<0.001). Apart from mRNA and sperm morphology (τ=0.325, p<0.05; ρ=0.461, p<0.05), no additional correlations were found between the levels of these transcripts and other conventional sperm parameters.
and mRNAs were found to be present in human spermatozoa and their transcription levels were positively correlated with sperm concentration and total sperm count. Spermatozoa are the only source of mRNA since is a paternally-inherited gene. Further studies are needed to evaluate its role in human fertilization.
少精子症在全球范围内高度流行。研究报告称,少精子症患者精子水平的差异甲基化区域的甲基化率低于对照组。[具体基因名称]是最著名的一对印记基因。然而,尚无研究评估它们是否在人类精子中转录。为了评估[具体基因名称]mRNA是否存在于人类精子中,以及它们的水平是否与精子浓度和总精子数相关。
精子样本(n = 22)使用特异性引物进行逆转录定量聚合酶链反应,以检测[具体基因名称]mRNA水平。然后使用Spearman(τ)和Kendall(ρ)秩相关系数将它们与患者的常规精子参数相关联。
发现[具体基因名称]mRNA水平与精子浓度(τ = 0.403,p < 0.01;ρ = 0.587,p < 0.005)和总精子数(τ = 0.347,p < 0.024;ρ = 0.509,p < 0.015)之间存在统计学上显著的正相关。[具体基因名称]mRNA水平与精子浓度(τ = 0.595,p < 0.001;ρ = 0.774,p < 0.001)和总精子数(τ = 0.547,p < 0.001;ρ = 0.701,p < 0.001)呈正相关。除了[具体基因名称]mRNA与精子形态(τ = (此处原文似乎不完整),p < 0.05;ρ = 0.461,p < 0.05)外,在这些转录本水平与其他常规精子参数之间未发现其他相关性。
发现[具体基因名称]mRNA存在于人类精子中,并且它们的转录水平与精子浓度和总精子数呈正相关。由于[具体基因名称]是父系遗传基因,精子是[具体基因名称]mRNA的唯一来源。需要进一步研究以评估其在人类受精中的作用。