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Publication : AUUUA sequences direct mRNA deadenylation uncoupled from decay during Xenopus early development.

First Author  Voeltz GK Year  1998
Journal  Mol Cell Biol Volume  18
Issue  12 Pages  7537-45
PubMed ID  9819439 Mgi Jnum  J:51059
Mgi Id  MGI:1314540 Doi  10.1128/mcb.18.12.7537
Citation  Voeltz GK, et al. (1998) AUUUA sequences direct mRNA deadenylation uncoupled from decay during Xenopus early development. Mol Cell Biol 18(12):7537-45
abstractText  To study the regulation of AUUUA-mediated RNA deadenylation and destabilization during Xenopus early development, we microinjected chimeric mRNAs containing Xenopus or mammalian 3' untranslated region (3'-UTR) sequences into Xenopus oocytes, mature eggs, or fertilized embryos. We found that the AU-rich elements (ARE) of Xenopus c-myc II and the human granulocyte-macrophage colony-stimulating factor gene (GMCSF) both direct deadenylation of chimeric mRNAs in an AUUUA- dependent manner. In the case of the Xenopus c-myc II ARE, mutation of a single AUUUA within an absolutely conserved 11-nucleotide region in c- myc 3'-UTRs prevents ARE-mediated deadenylation. AUUUA-specific deadenylation appears to be developmentally regulated: low deadenylation activity is observed in the oocyte, whereas rapid deadenylation occurs following egg activation or fertilization. Deadenylation results in the accumulation of stable deadenylated RNAs that become degraded only following mid-blastula transition. We conclude that ARE-mediated mRNA deadenylation can be uncoupled from ARE- mediated mRNA decay and that AUUUAs directly signal deadenylation during Xenopus early development.
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