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Stella modulates transcriptional and endogenous retrovirus programs during maternal-to-zygotic transition

The maternal-to-zygotic transition (MZT) marks the period when the embryonic genome is activated and acquires control of development. Maternally inherited factors play a key role in this critical developmental process, which occurs at the 2-cell stage in mice. We investigated the function of the mat...

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Detalles Bibliográficos
Autores principales: Huang, Yun, Kim, Jong Kyoung, Do, Dang Vinh, Lee, Caroline, Penfold, Christopher A, Zylicz, Jan J, Marioni, John C, Hackett, Jamie A, Surani, M Azim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404928/
https://www.ncbi.nlm.nih.gov/pubmed/28323615
http://dx.doi.org/10.7554/eLife.22345
Descripción
Sumario:The maternal-to-zygotic transition (MZT) marks the period when the embryonic genome is activated and acquires control of development. Maternally inherited factors play a key role in this critical developmental process, which occurs at the 2-cell stage in mice. We investigated the function of the maternally inherited factor Stella (encoded by Dppa3) using single-cell/embryo approaches. We show that loss of maternal Stella results in widespread transcriptional mis-regulation and a partial failure of MZT. Strikingly, activation of endogenous retroviruses (ERVs) is significantly impaired in Stella maternal/zygotic knockout embryos, which in turn leads to a failure to upregulate chimeric transcripts. Amongst ERVs, MuERV-L activation is particularly affected by the absence of Stella, and direct in vivo knockdown of MuERV-L impacts the developmental potential of the embryo. We propose that Stella is involved in ensuring activation of ERVs, which themselves play a potentially key role during early development, either directly or through influencing embryonic gene expression. DOI: http://dx.doi.org/10.7554/eLife.22345.001