Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription

Summary: Nuclear transfer systems represent the efficient means to reprogram a cell and in theory provide a basis for investigating the development of endangered species. However, conventional nuclear transfer using oocytes of laboratory animals does not allow reprogramming of cross-species nuclei o...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Junko Tomikawa, Christopher A. Penfold, Takuma Kamiya, Risa Hibino, Ayumi Kosaka, Masayuki Anzai, Kazuya Matsumoto, Kei Miyamoto
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
Materias:
Q
Acceso en línea:https://doaj.org/article/c7e3d6fbfc5345d496084183d44da4a4
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:c7e3d6fbfc5345d496084183d44da4a4
record_format dspace
spelling oai:doaj.org-article:c7e3d6fbfc5345d496084183d44da4a42021-11-20T05:09:29ZCell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription2589-004210.1016/j.isci.2021.103290https://doaj.org/article/c7e3d6fbfc5345d496084183d44da4a42021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589004221012591https://doaj.org/toc/2589-0042Summary: Nuclear transfer systems represent the efficient means to reprogram a cell and in theory provide a basis for investigating the development of endangered species. However, conventional nuclear transfer using oocytes of laboratory animals does not allow reprogramming of cross-species nuclei owing to defects in cell divisions and activation of embryonic genes. Here, we show that somatic nuclei transferred into mouse four-cell embryos arrested at the G2/M phase undergo reprogramming toward the embryonic state. Remarkably, genome-wide transcriptional reprogramming is induced within a day, and ZFP281 is important for this replication-free reprogramming. This system further enables transcriptional reprogramming of cells from Oryx dammah, now extinct in the wild. Thus, our findings indicate that arrested mouse embryos are competent to induce intra- and cross-species reprogramming. The direct induction of embryonic transcripts from diverse genomes paves a unique approach for identifying mechanisms of transcriptional reprogramming and genome activation from a diverse range of species.Junko TomikawaChristopher A. PenfoldTakuma KamiyaRisa HibinoAyumi KosakaMasayuki AnzaiKazuya MatsumotoKei MiyamotoElsevierarticleCell biologyStem cells researchDevelopmental biologyScienceQENiScience, Vol 24, Iss 11, Pp 103290- (2021)
institution DOAJ
collection DOAJ
language EN
topic Cell biology
Stem cells research
Developmental biology
Science
Q
spellingShingle Cell biology
Stem cells research
Developmental biology
Science
Q
Junko Tomikawa
Christopher A. Penfold
Takuma Kamiya
Risa Hibino
Ayumi Kosaka
Masayuki Anzai
Kazuya Matsumoto
Kei Miyamoto
Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription
description Summary: Nuclear transfer systems represent the efficient means to reprogram a cell and in theory provide a basis for investigating the development of endangered species. However, conventional nuclear transfer using oocytes of laboratory animals does not allow reprogramming of cross-species nuclei owing to defects in cell divisions and activation of embryonic genes. Here, we show that somatic nuclei transferred into mouse four-cell embryos arrested at the G2/M phase undergo reprogramming toward the embryonic state. Remarkably, genome-wide transcriptional reprogramming is induced within a day, and ZFP281 is important for this replication-free reprogramming. This system further enables transcriptional reprogramming of cells from Oryx dammah, now extinct in the wild. Thus, our findings indicate that arrested mouse embryos are competent to induce intra- and cross-species reprogramming. The direct induction of embryonic transcripts from diverse genomes paves a unique approach for identifying mechanisms of transcriptional reprogramming and genome activation from a diverse range of species.
format article
author Junko Tomikawa
Christopher A. Penfold
Takuma Kamiya
Risa Hibino
Ayumi Kosaka
Masayuki Anzai
Kazuya Matsumoto
Kei Miyamoto
author_facet Junko Tomikawa
Christopher A. Penfold
Takuma Kamiya
Risa Hibino
Ayumi Kosaka
Masayuki Anzai
Kazuya Matsumoto
Kei Miyamoto
author_sort Junko Tomikawa
title Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription
title_short Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription
title_full Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription
title_fullStr Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription
title_full_unstemmed Cell division- and DNA replication-free reprogramming of somatic nuclei for embryonic transcription
title_sort cell division- and dna replication-free reprogramming of somatic nuclei for embryonic transcription
publisher Elsevier
publishDate 2021
url https://doaj.org/article/c7e3d6fbfc5345d496084183d44da4a4
work_keys_str_mv AT junkotomikawa celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT christopherapenfold celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT takumakamiya celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT risahibino celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT ayumikosaka celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT masayukianzai celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT kazuyamatsumoto celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
AT keimiyamoto celldivisionanddnareplicationfreereprogrammingofsomaticnucleiforembryonictranscription
_version_ 1718419566552416256