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PLANT PHYSIOLOGY , Vol 106, Issue 2 537-546, Copyright © 1994 by American Society of Plant Biologists
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MOLECULAR BIOLOGY AND GENE REGULATION |
Leaf Developmental Age Controls Expression of Genes Encoding Enzymes of Chlorophyll and Heme Biosynthesis in Pea (Pisum sativum L.)
Z. H. He, J. Li, C. Sundqvist and M. P. Timko
Department of Biology, University of Virginia, Charlottesville, Virginia 22903 (Z.-H.H., J.L., M.P.T.)
The effects of leaf developmental age on the expression of three nuclear
gene families in pea (Pisum sativum L.) coding for enzymes of chlorophyll
and heme biosynthesis have been examined. The steady-state levels of mRNAs
encoding aminolevulinic acid (ALA) dehydratase, porphobilinogen (PBG)
deaminase, and NADPH:protochlorophyllide reductase were measured by RNA gel
blot and quantitative slot-blot analyses in the foliar leaves of embryos
that had imbibed for 12 to 18 h and leaves of developing seedlings grown
either in total darkness or under continuous white light for up to 14 d
after imbibition. Both ALA dehydratase and PBG deaminase mRNAs were
detectable in embryonic leaves, whereas mRNA encoding the
NADPH:protochlorophyllide reductase was not observed at this early
developmental stage. All three gene products were found to increase to
approximately the same extent in the primary leaves of pea seedlings during
the first 6 to 8 d after imbibition (postgermination) regardless of whether
the plants were grown in darkness or under continuous white-light
illumination. In the leaves of dark-grown seedlings, the highest levels of
message accumulation were observed at approximately 8 to 10 d
postgermination, and, thereafter, a steady decline in mRNA levels was
observed. In the leaves of light-grown seedlings, steady-state levels of
mRNA encoding the three chlorophyll biosynthetic enzymes were inversely
correlated with leaf age, with youngest, rapidly expanding leaves
containing the highest message levels. A corresponding increase in the
three enzyme protein levels was also found during the early stages of
development in the light or darkness; however, maximal accumulation of
protein was delayed relative to peak levels of mRNA accumulation. We also
found that although protochlorophyllide was detectable in the leaves
immediately after imbibition, the time course of accumulation of the
phototransformable form of the molecule coincided with
NADPH:protochlorophyllide reductase expression. In studies in which
dark-grown seedlings of various ages were subsequently transferred to light
for 24 and 48 h, the effect of light on changes in steady-state mRNA levels
was found to be more pronounced at later developmental stages. These
results suggest that the expression of these three genes and likely those
genes encoding other chlorophyll biosynthetic pathway enzymes are under the
control of a common regulatory mechanism. Furthermore, it appears that not
light, but rather as yet unidentified endogenous factors, are the primary
regulatory factors controlling gene expression early in leaf development.
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