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Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice

机译:P63对小鼠雄性生殖细胞凋亡和精子形成三个阶段的转录调控

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摘要

Infertility affects 10–15% of couples worldwide, and male factors account for 50%. Spermatogenesis is precisely regulated by genetic factors, and the mutations of genes result in abnormal spermatogenesis and eventual male infertility. The aim of this study was to explore the role and transcriptional regulation of P63 in the apoptosis and mouse spermatogenesis. P63 protein was decreased in male germ cells of P63(+/−) mice compared with wild-type mice. There was no obvious difference in testis weight, sperm motility, and fecundity between P63(+/−) and wild-type mice. However, abnormal germ cells were frequently observed in P63(+/−) mice at 2 months old. Notably, apoptotic male germ cells and the percentage of abnormal sperm were significantly enhanced in P63(+/−) mice compared to wild-type mice. Spermatogonia, pachytene spermatocytes and round spermatids were isolated from P63(+/−) and wild-type mice using STA-PUT velocity sedimentation, and they were identified phenotypically with high purities. RNA sequencing demonstrated distinct transcription profiles in spermatogonia, pachytene spermatocytes, and round spermatids between P63(+/−) mice and wild-type mice. In total, there were 645 differentially expressed genes (DEGs) in spermatogonia, 106 DEGs in pachytene spermatocytes, and 1152 in round spermatids between P63(+/−) mice and wild-type mice. Real time PCR verified a number of DEGs identified by RNA sequencing. Gene ontology annotation and pathway analyzes further indicated that certain key genes, e.g., Ccnd2, Tgfa, Hes5, Insl3, Kit, Lef1, and Jun were involved in apoptosis, while Dazl, Kit, Pld6, Cdkn2d, Stra8, and Ubr2 were associated with regulating spermatogenesis. Collectively, these results implicate that P63 mediates the apoptosis of male germ cells and regulates three stages of spermatogenesis transcriptionally. This study could provide novel targets for the diagnosis and treatment of male infertility.
机译:不孕症影响了全球10–15%的夫妻,男性因素占50%。精子发生受到遗传因素的精确调控,基因突变导致精子发生异常并最终导致男性不育。这项研究的目的是探讨P63在细胞凋亡和小鼠精子发生中的作用和转录调控。与野生型小鼠相比,P63 (+/-)小鼠雄性生殖细胞中的P63蛋白降低。 P63 (+/-)与野生型小鼠的睾丸重量,精子活力和生殖力无明显差异。然而,在2个月大的P63 (+/-)小鼠中经常观察到异常生殖细胞。值得注意的是,与野生型小鼠相比,P63 (+/-)小鼠的凋亡性雄性生殖细胞和异常精子的百分比显着提高。使用STA-PUT速度沉降法从P63 (+/-)和野生型小鼠中分离出精原细胞,粗精子细胞和圆形精子,并在表型上鉴定出高纯度。 RNA测序表明,P63 (+/-)小鼠和野生型小鼠的精原细胞,粗线精原细胞和圆形精子有明显的转录特征。在P63 (+/-)小鼠和野生型小鼠之间,精原细胞中共有645个差异表达基因(DEG),粗线精细胞中有106 DEG,圆形精子中有1152个。实时PCR验证了许多通过RNA测序鉴定的DEG。基因本体注释和途径分析进一步表明,某些关键基因,例如Ccnd2,Tgfa,Hes5,Insl3,Kit,Lef1和Jun参与凋亡,而Dazl,Kit,Pld6,Cdkn2d,Stra8和Ubr2与细胞凋亡相关。调节精子发生。总之,这些结果暗示P63介导男性生殖细胞的凋亡并在转录上调节精子发生的三个阶段。该研究可为男性不育的诊断和治疗提供新的靶点。

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