Non-coding RNAs as regulators of embryogenesis
By A. Pauli, Johannes Rinn, A. Schier. Nature reviews genetics, 2011
630 citations recorded by the source corpus.
Non-coding RNAs (ncRNAs) are emerging as key regulators of embryogenesis. They control embryonic gene expression by several means, ranging from microRNA-induced degradation of mRNAs to long ncRNA-mediated modification of chromatin. Many aspects of embryogenesis seem to be controlled by ncRNAs, including the maternal–zygotic transition, the maintenance of pluripotency, the patterning of the body axes, the specification and differentiation of cell types and the morphogenesis of organs. Drawing from several animal model systems, we describe two emerging themes for ncRNA function: promoting developmental transitions and maintaining developmental states. These examples also highlight the roles of ncRNAs in ensuring a robust commitment to one of two possible cell fates.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/46567205d584a0d9d39b1c730e1dd1d5eb22ae47
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Citations in the corpus
- Systematic identification of long noncoding RNAs expressed during zebrafish embryogenesis. (2012, background): “While miRNAs (microRNAs), the best-studied class of sRNAs, regulate their mRNA targets post- transcriptionally (Bartel 2009), mRNA-like lncRNAs act by a range of mechanisms (for reviews, see Koziol and Rinn 2010; Pauli et al. 2011; Wang and Chang 2011).”
- Gene regulation by the act of long non-coding RNA transcription (2013, background): “LncRNAs - a new layer of genome regulatory information It is now well appreciated that less than two percent of the human genome codes for proteins and the majority of the genome gives rise to non-protein-coding RNAs (ncRNAs) [1], which are predicted to play essential roles in a variety of biologica”
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- A double take on bivalent promoters. (2013, background): “Expression profiles of several types of ncRNAs suggest that they are involved in cell fate decisions (Jacquier 2009; Guttman et al. 2011; Pauli et al. 2011).”
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