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作为有丝分裂、减数分裂和精子发生的表观遗传调节因子的微小RNA和DNA甲基化。

MicroRNAs and DNA methylation as epigenetic regulators of mitosis, meiosis and spermiogenesis.

作者信息

Yao Chencheng, Liu Yun, Sun Min, Niu Minghui, Yuan Qingqing, Hai Yanan, Guo Ying, Chen Zheng, Hou Jingmei, Liu Yang, He Zuping

机构信息

State Key Laboratory of Oncogenes and Related GenesSchool of Medicine, Renji-Med X Clinical Stem Cell Research Center, Ren Ji Hospital, Shanghai Jiao Tong University, 160 Pujiang Road, Shanghai 200127, ChinaDepartment of UrologySchool of Medicine, Shanghai Institute of Andrology, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai Human Sperm Bank, 145 Shangdong Road, Shanghai 200001, ChinaShanghai Key Laboratory of Assisted Reproduction and Reproductive GeneticsShanghai 200127, ChinaShanghai Key Laboratory of Reproductive MedicineShanghai 200025, China.

State Key Laboratory of Oncogenes and Related GenesSchool of Medicine, Renji-Med X Clinical Stem Cell Research Center, Ren Ji Hospital, Shanghai Jiao Tong University, 160 Pujiang Road, Shanghai 200127, ChinaDepartment of UrologySchool of Medicine, Shanghai Institute of Andrology, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai Human Sperm Bank, 145 Shangdong Road, Shanghai 200001, ChinaShanghai Key Laboratory of Assisted Reproduction and Reproductive GeneticsShanghai 200127, ChinaShanghai Key Laboratory of Reproductive MedicineShanghai 200025, China State Key Laboratory of Oncogenes and Related GenesSchool of Medicine, Renji-Med X Clinical Stem Cell Research Center, Ren Ji Hospital, Shanghai Jiao Tong University, 160 Pujiang Road, Shanghai 200127, ChinaDepartment of UrologySchool of Medicine, Shanghai Institute of Andrology, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai Human Sperm Bank, 145 Shangdong Road, Shanghai 200001, ChinaShanghai Key Laboratory of Assisted Reproduction and Reproductive GeneticsShanghai 200127, ChinaShanghai Key Laboratory of Reproductive MedicineShanghai 200025, China State Key Laboratory of Oncogenes and Related GenesSchool of Medicine, Renji-Med X Clinical Stem Cell Research Center, Ren Ji Hospital, Shanghai Jiao Tong University, 160 Pujiang Road, Shanghai 200127, ChinaDepartment of UrologySchool of Medicine, Shanghai Institute of Andrology, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai Human Sperm Bank, 145 Shangdong Road, Shanghai 200001, ChinaShanghai Key Laboratory of Assisted Reproduction and Reproductive GeneticsShanghai 200127, ChinaShanghai Key Laboratory of Reproductive MedicineShanghai 200025, China State Key Laboratory of Oncogenes and Related GenesSchool of Medicine, Renji-Med X Clinical Stem Cell Research Center, Ren Ji Hospital, Shanghai Jiao Tong University, 160 Pujiang Road, Shanghai 200127, ChinaDepartment of UrologySchool of Medicine, Shanghai Institute of Andrology, Ren Ji Hospital, Shangha

出版信息

Reproduction. 2015 Jul;150(1):R25-34. doi: 10.1530/REP-14-0643. Epub 2015 Apr 7.

Abstract

Spermatogenesis is composed of three distinctive phases, which include self-renewal of spermatogonia via mitosis, spermatocytes undergoing meiosis I/II and post-meiotic development of haploid spermatids via spermiogenesis. Spermatogenesis also involves condensation of chromatin in the spermatid head before transformation of spermatids to spermatozoa. Epigenetic regulation refers to changes of heritably cellular and physiological traits not caused by modifications in the DNA sequences of the chromatin such as mutations. Major advances have been made in the epigenetic regulation of spermatogenesis. In this review, we address the roles and mechanisms of epigenetic regulators, with a focus on the role of microRNAs and DNA methylation during mitosis, meiosis and spermiogenesis. We also highlight issues that deserve attention for further investigation on the epigenetic regulation of spermatogenesis. More importantly, a thorough understanding of the epigenetic regulation in spermatogenesis will provide insightful information into the etiology of some unexplained infertility, offering new approaches for the treatment of male infertility.

摘要

精子发生由三个不同阶段组成,包括精原细胞通过有丝分裂进行自我更新、精母细胞经历减数分裂I/II以及单倍体精子细胞通过精子形成进行减数分裂后发育。精子发生还涉及在精子细胞转变为精子之前精子细胞核中染色质的浓缩。表观遗传调控是指由染色质DNA序列修饰(如突变)以外的可遗传细胞和生理特征变化。精子发生的表观遗传调控已取得重大进展。在本综述中,我们阐述了表观遗传调节因子的作用和机制,重点关注有丝分裂、减数分裂和精子形成过程中微小RNA和DNA甲基化的作用。我们还强调了精子发生表观遗传调控进一步研究中值得关注的问题。更重要的是,深入了解精子发生中的表观遗传调控将为一些不明原因不孕症的病因提供有价值的信息,为男性不育症的治疗提供新方法。

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