Plant Physiol, May 2002, Vol. 129, pp. 342-353
The 5'-Untranslated Region of the ntp303 Gene
Strongly Enhances Translation during Pollen Tube Growth, But Not during
Pollen Maturation
Raymond J.M.
Hulzink,
Peter F.M.
de Groot,
Anton F.
Croes,
William
Quaedvlieg,
Dave
Twell,
George J.
Wullems, and
Marinus M.A.
van
Herpen*
Department of Experimental Botany, Plant Genetics, Catholic
University Nijmegen, Toernooiveld 1, 6525 ED, Nijmegen, The Netherlands
(R.J.M.H., P.F.M.d.G., A.F.C., W.Q., G.J.W., M.M.A.v.H.); and
Department of Biology, University of Leicester, University Road,
Leicester, LE17RH, United Kingdom (D.T.)
Transcripts of the ntp303 gene accumulate
abundantly throughout pollen development, whereas the protein only
accumulates to detectable levels after pollen germination. In an
attempt to explain the divergence in the accumulation profiles of the
mRNA and the protein, we investigated the role of the untranslated
regions (UTRs) in enhancing ntp303 translation
during the transition from developing to germinating pollen. Luciferase
reporter gene fusion constructs containing the ntp303
5'-UTR gave rise to luciferase activity that was up to 60-fold higher
during pollen tube growth than that of constructs containing different
5'-UTRs. No apparent differences in the luciferase activity of these
constructs were observed during pollen development. The
ntp303 5'-UTR-mediated increase in luciferase activity
was not significantly influenced by coding region or 3'-UTR sequences.
Furthermore, enhanced luciferase activity directed by the
ntp303 5'-UTR occurred predominantly at the
post-transcriptional level. A series of 5'-UTR deletion constructs was
created to identify putative regulatory sequences required for the high
level of translation during pollen tube growth. Two predicted stem loop
structures (H-I and H-II) caused a complete inhibition of the enhanced
translation after their total or partial deletion. A (GAA)8
repeat within the H-I stem loop structure was demonstrated to be
important for the modulation of translation efficiency. The H-II stem
loop structure was found to be essential for the determination of mRNA stability.
*
Corresponding author; e-mail marinush{at}sci.kun.nl; fax
31-0-24-3553450.
© 2002 American Society of Plant Physiologists