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PMID: 3387433 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Localization and conditional redundancy of regulatory elements in rbcS-3A, a pea gene encoding the small subunit of ribulose-bisphosphate carboxylase.

Kuhlemeier C, Cuozzo M, Green PJ, Goyvaerts E, Ward K, Chua NH

Abstract

Expression of the pea rbcS-3A gene, one of a family of genes encoding the small subunit of ribulose-bisphosphate carboxylase [EC 4.1.1.39], is regulated by light and is restricted to chloroplast-containing cells. We analyzed the effects of light and development on rbcS-3A expression in transgenic plants. Two highly conserved sequences ("boxes" II and III) around nucleotide position -150 (relative to the transcription initiation site, +1) are required for rbcS-3A expression. The so-defined positive elements overlap with previously identified negative light-regulatory elements. In the case of box II, which has sequence similarity to the core enhancer motif of simian virus 40, a GG----CC transversion is sufficient to abolish expression. The effect of mutations in boxes II and III can only be measured when sequences upstream of -170 are removed, and because sequences both 5' and 3' of -170 can direct light-regulated and organ-specific expression. This implies that there is a redundancy of cis-acting elements in the 5' noncoding region of rbcS-3A. However, we show that the sequences upstream of -170 are dispensable only in the mature leaves of a green plant. In contrast, in the young, expanding leaves at the top of a green plant, as well as in seedlings, the distal elements are required for high-level expression. Therefore, redundancy is not absolute, and the requirements for rbcS-3A expression change during plant development.

MeSH Terms
Base Sequence Fabaceae/enzymology,genetics Genes/radiation effects Light Molecular Sequence Data Organ Specificity Plant Proteins/genetics Plants, Medicinal Regulatory Sequences, Nucleic Acid/radiation effects Ribulose-Bisphosphate Carboxylase/genetics
Chemicals
Plant Proteins Ribulose-Bisphosphate Carboxylase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kuhlemeier C
Laboratory of Plant Molecular Biology, Rockefeller University, New York, NY 10021-6399.
Cuozzo M
Green P J
Goyvaerts E
Ward K
Chua N H
References (16)
16 references, click to expand
  1. Expression dynamics of the pea rbcS multigene family and organ distribution of the transcripts.
    EMBO J. 1986 Sep;5(9):2063-2071 PMID: 16453702
  2. The human beta-interferon gene enhancer is under negative control.
    Cell. 1986 May 23;45(4):601-10 PMID: 3708688
  3. Organ-specific and light-induced expression of plant genes.
    Science. 1986 May 30;232(4754):1106-12 PMID: 17754498
  4. The SV40 enhancer is composed of multiple functional elements that can compensate for one another.
    Cell. 1986 May 9;45(3):461-70 PMID: 3009027
  5. Sequences in the pea rbcS-3A gene have homology to constitutive mammalian enhancers but function as negative regulatory elements.
    Genes Dev. 1987 May;1(3):247-55 PMID: 2890552
  6. Ti plasmid vector for the introduction of DNA into plant cells without alteration of their normal regeneration capacity.
    EMBO J. 1983;2(12):2143-50 PMID: 16453482
  7. Sequence-specific interactions of a pea nuclear factor with light-responsive elements upstream of the rbcS-3A gene.
    EMBO J. 1987 Sep;6(9):2543-9 PMID: 3678200
  8. Binary Agrobacterium vectors for plant transformation.
    Nucleic Acids Res. 1984 Nov 26;12(22):8711-21 PMID: 6095209
  9. Developmental regulation of two genes encoding ribulose-bisphosphate carboxylase small subunit in pea and transgenic petunia plants: Phytochrome response and blue-light induction.
    Proc Natl Acad Sci U S A. 1986 Apr;83(8):2358-62 PMID: 16593682
  10. Tissue-specific and light-regulated expression of a pea nuclear gene encoding the small subunit of ribulose-1,5-bisphosphate carboxylase.
    EMBO J. 1984 Aug;3(8):1671-9 PMID: 6479146
  11. Interferon-beta gene regulation: tandemly repeated sequences of a synthetic 6 bp oligomer function as a virus-inducible enhancer.
    Cell. 1987 May 8;49(3):357-67 PMID: 3032451
  12. Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells.
    Mol Cell Biol. 1982 Sep;2(9):1044-51 PMID: 6960240
  13. Diversity of alpha-fetoprotein gene expression in mice is generated by a combination of separate enhancer elements.
    Science. 1987 Jan 2;235(4784):53-8 PMID: 2432657
  14. A simple and general method for transferring genes into plants.
    Science. 1985 Mar 8;227(4691):1229-31 PMID: 17757866
  15. Multiple sequence motifs are involved in SV40 enhancer function.
    EMBO J. 1986 Feb;5(2):387-97 PMID: 3011406
  16. Identification of two distinct regulatory regions adjacent to the human beta-interferon gene.
    Cell. 1983 Oct;34(3):865-79 PMID: 6313211
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1988-07-00
Pages
4662-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC280495
Subset
IM
Grants
NIGMS NIH HHS · GM10853 · United States
NIGMS NIH HHS · GM11797 · United States
Databases
GENBANK
M21356
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