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Molecular and Cellular Biology, December 1998, p. 7537-7545, Vol. 18, No. 12
Department of Molecular Biophysics and
Biochemistry, Howard Hughes Medical Institute, Yale University, New
Haven, Connecticut 06536
Received 6 July 1998/Returned for modification 21 July
1998/Accepted 23 August 1998
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.
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
AUUUA Sequences Direct mRNA Deadenylation Uncoupled
from Decay during Xenopus Early Development
*
Corresponding author. Mailing address: Department of
Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University, 295 Congress Ave., New Haven, CT 06536. Phone: (203)
737-4417. Fax: (203) 624-8213. E-mail: joan.steitz{at}yale.edu.
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