Literature DB >> 18386827

Erasure of the paternal transcription program during spermiogenesis: the first step in the reprogramming of sperm chromatin for zygotic development.

Junke Zheng1, Xiaoyu Xia, Hui Ding, Ayong Yan, Shaunggang Hu, Xun Gong, Shudong Zong, Yonglian Zhang, Hui Z Sheng.   

Abstract

Male germ cells possess a unique epigenetic program and express a male-specific transcription profile. However, when its chromatin is passed onto the zygote, it expresses an transcription/epigenetic program characteristic of the zygote. The mechanism underlying this reprogramming process is not understood at present. In this study, we show that an extensive range of chromatin factors (CFs), including essential transcription factors and regulators, remodeling factors, histone deacetylases, heterochromatin-binding proteins, and topoisomerases, were removed from chromatin during spermiogenesis. This process will erase the paternal epigenetic program to generate a relatively naive chromatin, which is likely to be essential for installation of the zygotic developmental program after fertilization. We have also showed that transcription termination in male germ cells was temporally correlated with CF dissociation. A genome-wide CF dissociation will inevitably disassemble the transcription apparatus and regulatory mechanism and lead to transcription silence. Based on data presented in this and previous studies (Sun et al., Cell Research [2007] 17:117-134), we propose that paternal-zygotic transcription reprogramming begins with a genome-wide CF dissociation to erase the existing transcription program in later stages of spermatogenesis. This will be followed by assembling of the zygotic equivalent after fertilization. The transcription/epigenetic program of the male germ cell is transformed into a zygotic one using an erase-and-rebuild strategy similar to that used in the maternal-zygotic transition. It is also noted that transcription is terminated long after meiosis is completed and before chromatin becomes highly condensed during spermatogenesis. The temporal order of these events suggests that transcription silence does not have to be coupled to meiosis or chromatin condensation.

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Year:  2008        PMID: 18386827     DOI: 10.1002/dvdy.21499

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  13 in total

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4.  Aberrant levels of histone H3 acetylation induce spermatid anomaly in mouse testis.

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7.  Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.

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Review 8.  Spermatogonial stem cells, infertility and testicular cancer.

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9.  Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice.

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10.  Nuclear reprogramming of sperm and somatic nuclei in eggs and oocytes.

Authors:  Marta Teperek; Kei Miyamoto
Journal:  Reprod Med Biol       Date:  2013-06-04
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