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Expanding the repertoire of deadenylases.
- Source :
-
RNA biology [RNA Biol] 2017 Oct 03; Vol. 14 (10), pp. 1320-1325. Date of Electronic Publication: 2017 Mar 07. - Publication Year :
- 2017
-
Abstract
- Deadenylases belong to an expanding family of exoribonucleases involved mainly in mRNA stability and turnover, with the exception of PARN which has additional roles in the biogenesis of several important non-coding RNAs, including miRNAs and piRNAs. Recently, PARN in C. elegans and its homolog PNLDC1 in B. mori were reported as the elusive trimmers mediating piRNA biogenesis. In addition, characterization of mammalian PNLDC1 in comparison to PARN, showed that is specifically expressed in embryonic stem and germ cells, as well as during early embryo development. Moreover, its expression is correlated with epigenetic events mediated by the de novo DNMT3b methyltransferase and knockdown in stem cells upregulates important genes that regulate multipotency. The recent data suggest that at least some new deadenylases may have expanded roles in cell metabolism as regulators of gene expression, through mRNA deadenylation, ncRNAs biogenesis and ncRNA-mediated mRNA targeting, linking essential mechanisms that regulate epigenetic control and transition events during differentiation. The possible roles of mammalian PNLDC1 along those dynamic networks are discussed in the light of new extremely important findings.
- Subjects :
- Animals
Bombyx enzymology
Bombyx growth & development
Caenorhabditis elegans enzymology
Caenorhabditis elegans growth & development
DNA (Cytosine-5-)-Methyltransferases metabolism
Gene Expression Regulation, Developmental
Gene Regulatory Networks
Humans
RNA Stability
RNA, Messenger chemistry
RNA, Small Interfering metabolism
DNA Methyltransferase 3B
Epigenesis, Genetic
Exoribonucleases metabolism
Gene Expression
Subjects
Details
- Language :
- English
- ISSN :
- 1555-8584
- Volume :
- 14
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- RNA biology
- Publication Type :
- Academic Journal
- Accession number :
- 28267419
- Full Text :
- https://doi.org/10.1080/15476286.2017.1300222