Plant Physiol. Drug Metab Dispos
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by He, Z. H.
Right arrow Articles by Timko, M. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by He, Z. H.
Right arrow Articles by Timko, M. P.
Agricola
Right arrow Articles by He, Z. H.
Right arrow Articles by Timko, M. P.

PLANT PHYSIOLOGY , Vol 106, Issue 2 537-546, Copyright © 1994 by American Society of Plant Biologists


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.


This article has been cited by other articles:


Home page
Mol PlantHome page
M. Huang, T. L. Slewinski, R. F. Baker, D. Janick-Buckner, B. Buckner, G. S. Johal, and D. M. Braun
Camouflage Patterning in Maize Leaves Results from a Defect in Porphobilinogen Deaminase
Mol Plant, July 1, 2009; 2(4): 773 - 789.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
F. Matsumoto, T. Obayashi, Y. Sasaki-Sekimoto, H. Ohta, K.-i. Takamiya, and T. Masuda
Gene Expression Profiling of the Tetrapyrrole Metabolic Pathway in Arabidopsis with a Mini-Array System
Plant Physiology, August 1, 2004; 135(4): 2379 - 2391.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
M. Seyedi, M. P. Timko, and C. Sundqvist
The Distribution of Protochlorophyllide and Chlorophyll within Seedlings of the lip1 Mutant of Pea
Plant Cell Physiol., September 1, 2001; 42(9): 931 - 941.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. M. Quinn, S. S. Nakamoto, and S. Merchant
Induction of Coproporphyrinogen Oxidase in Chlamydomonas Chloroplasts Occurs via Transcriptional Regulation of Cpx1 Mediated by Copper Response Elements and Increased Translation from a Copper Deficiency-specific Form of the Transcript
J. Biol. Chem., May 14, 1999; 274(20): 14444 - 14454.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
G. Hu, N. Yalpani, S. P. Briggs, and G. S. Johal
A Porphyrin Pathway Impairment Is Responsible for the Phenotype of a Dominant Disease Lesion Mimic Mutant of Maize
PLANT CELL, July 1, 1998; 10(7): 1095 - 1106.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
T. Leustek, M. Smith, M. Murillo, D. P. Singh, A. G. Smith, S. C. Woodcock, S. J. Awan, and M. J. Warren
Siroheme Biosynthesis in Higher Plants. ANALYSIS OF AN S-ADENOSYL-L-METHIONINE-DEPENDENT UROPORPHYRINOGEN III METHYLTRANSFERASE FROM ARABIDOPSIS THALIANA
J. Biol. Chem., January 31, 1997; 272(5): 2744 - 2752.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1994 by the American Society of Plant Biologists