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Mol. Cell. Biol., Jun 1995, 3344-3353, Vol 15, No. 6
S Plaza, C Dozier, N Turque and S Saule
During investigations on the regulation of the Pax-6 gene, we characterized
a cDNA from quail neuroretina showing a 5' untranslated region distinct
from that previously described and initiated from an internal promoter.
Using RNase protection and primer extension mapping, we localized this
second quail Pax-6 promoter, termed P1. As reported for the already
described P0 promoter, P1 was also transactivated in vitro by the
p46Pax-QNR protein. RNase protection assays performed with quail
neuroretina RNA showed that P1-initiated mRNAs were detected before the
P0-initiated mRNAs, remained constant up to embryonic day 8, and decreased
slowly thereafter whereas, P0-initiated mRNAs accumulated up to embryonic
day 8. In contrast, quail retinal pigmented epithelium expressed only the
P1-initiated mRNAs. Transformation of these cells by the v-myc oncogene
induced neuronal traits in the culture, which thereafter, in addition to
the P1-initiated mRNAs, expressed Pax-QNR from the P0 promoter. These
results suggest that expression of the quail Pax-6 gene is under the
control of different regulators through alternate promoters, P0 being
activated at the onset of neuronal differentiation.
Copyright © 1995, American Society for Microbiology
Quail Pax-6 (Pax-QNR) mRNAs are expressed from two promoters used differentially during retina development and neuronal differentiation
Laboratoire de Differenciation Cellulaire et Moleculaire, CNRS EP56, Institute Pasteur, Lille, France.
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