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New Arabidopsis cue Mutants Suggest a Close
Connection between Plastid- and Phytochrome Regulation of Nuclear Gene
Expression1
Enrique López-Juez,
R. Paul Jarvis,
Atsuko Takeuchi,
Anton M. Page, and
Joanne Chory*
Plant Biology Laboratory (E.L.-J., R.P.J., A.T., J.C.), and Howard
Hughes Medical Institute (J.C.), The Salk Institute, 10010 North Torrey
Pines Road, La Jolla, California 92037; and The Salk Institute, 10010 North Torrey
Pines Road, La Jolla, California 92037School of Biological
Sciences, Royal Holloway, University of London, Egham, Surrey TW20 0EX,
United Kingdom (E.L.-J., A.M.P.)
We searched for new components that
are involved in the positive regulation of nuclear gene expression by
light by extending a screen for Arabidopsis cue
(chlorophyll a/b-binding
[CAB] protein-underexpressed) mutants (H.-M.
Li, K. Culligan, R.A. Dixon, J. Chory [1995] Plant Cell
7: 1599-1610). cue mutants display reduced expression
of the CAB3 gene, which encodes light-harvesting
chlorophyll protein, the main chloroplast antenna. The new mutants can
be divided into (a) phytochrome-deficient mutants (hy1
and phyB), (b) virescent or delayed-greening mutants
(cue3, cue6, and cue8),
and (c) uniformly pale mutants (cue4 and
cue9). For each of the mutants, the reduction in
CAB expression correlates with the visible phenotype,
defective chloroplast development, and reduced abundance of the
light-harvesting chlorophyll protein. Levels of protochlorophyllide
oxidoreductase (POR) were reduced to varying degrees in etiolated
mutant seedlings. In the dark, whereas the virescent mutants displayed
reduced CAB expression and the lowest levels of POR
protein, the other mutants expressed CAB and accumulated
POR at near wild-type levels. All of the mutants, with the exception of
cue6, were compromised in their ability to derepress
CAB expression in response to phytochrome activation.
Based on these results, we propose that the previously postulated
plastid-derived signal is closely involved in the pathway through which
phytochrome regulates the expression of nuclear genes encoding plastid
proteins.
1
This work was supported by a grant from the U.S.
Department of Energy (no. ER13993 to J.C.). While at The Salk
Institute, E.L.-J. was a fellow of the Spanish Ministry of Education
and of the North Atlantic Treaty Organization. R.P.J. is a long-term fellow of the International Human Frontier Science Program
Organization. J.C. is an associate investigator at the Howard Hughes
Medical Institute.
*
Corresponding author; e-mail chory{at}salk.edu; fax
1-619-558-6379.
Plant Physiol. (1998) 118: 803-815
Copyright Clearance Center: 0032-0889/98/118//13
© 1998 American Society of Plant Physiologists
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