Functional roles of non-coding Y RNAs.
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Publication Date
2015-09Journal Title
Int J Biochem Cell Biol
ISSN
1357-2725
Publisher
Elsevier
Volume
66
Pages
20-29
Language
English
Type
Article
Metadata
Show full item recordCitation
Kowalski, M. P., & Krude, T. (2015). Functional roles of non-coding Y RNAs.. Int J Biochem Cell Biol, 66 20-29. https://doi.org/10.1016/j.biocel.2015.07.003
Abstract
Non-coding RNAs are involved in a multitude of cellular processes but the biochemical function of many small non-coding RNAs remains unclear. The family of small non-coding Y RNAs is conserved in vertebrates and related RNAs are present in some prokaryotic species. Y RNAs are also homologous to the newly identified family of non-coding stem-bulge RNAs (sbRNAs) in nematodes, for which potential physiological functions are only now emerging. Y RNAs are essential for the initiation of chromosomal DNA replication in vertebrates and, when bound to the Ro60 protein, they are involved in RNA stability and cellular responses to stress in several eukaryotic and prokaryotic species. Additionally, short fragments of Y RNAs have recently been identified as abundant components in the blood and tissues of humans and other mammals, with potential diagnostic value. While the number of functional roles of Y RNAs is growing, it is becoming increasingly clear that the conserved structural domains of Y RNAs are essential for distinct cellular functions. Here, we review the biochemical functions associated with these structural RNA domains, as well as the functional conservation of Y RNAs in different species. The existing biochemical and structural evidence supports a domain model for these small non-coding RNAs that has direct implications for the modular evolution of functional non-coding RNAs.
Keywords
DNA replication, Non-coding RNA, RNA domains, RNA stability, Y RNA, Animals, Base Sequence, DNA Replication, Humans, Models, Molecular, Molecular Sequence Data, Nucleic Acid Conformation, RNA, Untranslated, Ribonucleoproteins
Sponsorship
Research in the authors’ laboratory has been funded by grants from Cancer Research UK (CRUK), the Association for International Cancer Research (AICR) and the Biotechnology and Biological Sciences Research Council (BBSRC).
Funder references
Worldwide Cancer Research (10-0570)
BBSRC (BB/K013378/1)
Identifiers
External DOI: https://doi.org/10.1016/j.biocel.2015.07.003
This record's URL: https://www.repository.cam.ac.uk/handle/1810/248909
Rights
Attribution 2.0 UK: England & Wales
Licence URL: http://creativecommons.org/licenses/by/2.0/uk/
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