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Endogenous Retroviruses Function as Gene Expression Regulatory Elements During Mammalian Pre-implantation Embryo Development

期刊

出版社

MDPI
DOI: 10.3390/ijms20030790

关键词

pre-implantation embryo; endogenous retroviruses; zygotic genome activation; epigenetic reprogramming; somatic cell nuclear transfer

资金

  1. Heilongjiang Academy of Agricultural Sciences Incubation Project for National Natural Science Foundation of China [2018JJPY001]
  2. Heilongjiang Academy of Agricultural Sciences Doctoral Scientific Research Project [201507-32]
  3. Postdoctoral Scientific Research Project of Heilongjiang Province [LBH-Q15130]
  4. National Natural Science Foundation of China [31872980, 31671289, 31201804]
  5. China Agricultural Research System [CARS-37]
  6. Project for Improving Innovative Capability of Scientific Institutions in Heilongjiang Province [YC2016D001]
  7. Natural Science Foundation of Heilongjiang Province of China [JJ2018ZZ0082]

向作者/读者索取更多资源

Pre-implantation embryo development encompasses several key developmental events, especially the activation of zygotic genome activation (ZGA)-related genes. Endogenous retroviruses (ERVs), which are regarded as deleterious genomic parasites, were previously considered to be junk DNA. However, it is now known that ERVs, with limited conservatism across species, mediate conserved developmental processes (e.g., ZGA). Transcriptional activation of ERVs occurs during the transition from maternal control to zygotic genome control, signifying ZGA. ERVs are versatile participants in rewiring gene expression networks during epigenetic reprogramming. Particularly, a subtle balance exists between ERV activation and ERV repression in host-virus interplay, which leads to stage-specific ERV expression during pre-implantation embryo development. A large portion of somatic cell nuclear transfer (SCNT) embryos display developmental arrest and ZGA failure during pre-implantation embryo development. Furthermore, because of the close relationship between ERV activation and ZGA, exploring the regulatory mechanism underlying ERV activation may also shed more light on the enigma of SCNT embryo development in model animals.

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