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THE PLANT CELL, Vol 2, Issue 4 279-289, Copyright © 1990 by American Society of Plant Biologists
Introduction of a Chimeric Chalcone Synthase Gene into Petunia Results in Reversible Co-Suppression of Homologous Genes in trans
C. Napoli, C. Lemieux and R. Jorgensen
DNA Plant Technology Corporation, 6701 San Pablo Avenue, Oakland, California 94608
We attempted to overexpress chalcone synthase (CHS) in pigmented petunia
petals by introducing a chimeric petunia CHS gene. Unexpectedly, the
introduced gene created a block in anthocyanin biosynthesis. Forty-two
percent of plants with the introduced CHS gene produced totally white
flowers and/or patterned flowers with white or pale nonclonal sectors on a
wild-type pigmented background; none of hundreds of transgenic control
plants exhibited such phenotypes. Progeny testing of one plant demonstrated
that the novel color phenotype co-segregated with the introduced CHS gene;
progeny without this gene were phenotypically wild type. The somatic and
germinal stability of the novel color patterns was variable. RNase
protection analysis of petal RNAs isolated from white flowers showed that,
although the developmental timing of mRNA expression of the endogenous CHS
gene was not altered, the level of the mRNA produced by this gene was
reduced 50-fold from wild-type levels. Somatic reversion of plants with
white flowers to phenotypically parental violet flowers was associated with
a coordinate rise in the steady-state levels of the mRNAs produced by both
the endogenous and the introduced CHS genes. Thus, in the altered white
flowers, the expression of both genes was coordinately suppressed,
indicating that expression of the introduced CHS gene was not alone
sufficient for suppression of endogenous CHS transcript levels. The
mechanism responsible for the reversible co-suppression of homologous genes
in trans is unclear, but the erratic and reversible nature of this
phenomenon suggests the possible involvement of methylation.
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J. Downward
RNA interference
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E. Bucher, H. Hemmes, P. de Haan, R. Goldbach, and M. Prins
The influenza A virus NS1 protein binds small interfering RNAs and suppresses RNA silencing in plants
J. Gen. Virol.,
April 1, 2004;
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[Abstract]
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J.-F. Wang, H. Zhou, Y.-Q. Chen, Q.-J. Luo, and L.-H. Qu
Identification of 20 microRNAs from Oryza sativa
Nucleic Acids Res.,
March 12, 2004;
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[Abstract]
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A.J. HERR and D.C. BAULCOMBE
RNA Silencing Pathways in Plants
Cold Spring Harb Symp Quant Biol,
January 1, 2004;
69(0):
363 - 370.
[Abstract]
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M. PAL-BHADRA, U. BHADRA, and J.A. BIRCHLER
Interrelationship of RNA Interference and Transcriptional Gene Silencing in Drosophila
Cold Spring Harb Symp Quant Biol,
January 1, 2004;
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433 - 438.
[Abstract]
[PDF]
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N. Agrawal, P. V. N. Dasaradhi, A. Mohmmed, P. Malhotra, R. K. Bhatnagar, and S. K. Mukherjee
RNA Interference: Biology, Mechanism, and Applications
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[Abstract]
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O. Milhavet, D. S. Gary, and M. P. Mattson
RNA Interference in Biology and Medicine
Pharmacol. Rev.,
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M. Vandenbussche, J. Zethof, E. Souer, R. Koes, G. B. Tornielli, M. Pezzotti, S. Ferrario, G. C. Angenent, and T. Gerats
Toward the Analysis of the Petunia MADS Box Gene Family by Reverse and Forward Transposon Insertion Mutagenesis Approaches: B, C, and D Floral Organ Identity Functions Require SEPALLATA-Like MADS Box Genes in Petunia
PLANT CELL,
November 1, 2003;
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2680 - 2693.
[Abstract]
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[PDF]
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H. Lee, J. L. Humann, J. S. Pitrak, J. T. Cuperus, T. D. Parks, C. A. Whistler, M. C. Mok, and L. W. Ream
Translation Start Sequences Affect the Efficiency of Silencing of Agrobacterium tumefaciens T-DNA Oncogenes
Plant Physiology,
November 1, 2003;
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C. Simon-Mateo, J. J. Lopez-Moya, H. S. Guo, E. Gonzalez, and J. A. Garcia
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R. Vanitharani, P. Chellappan, and C. M. Fauquet
Short interfering RNA-mediated interference of gene expression and viral DNA accumulation in cultured plant cells
PNAS,
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L. Gitlin and R. Andino
Nucleic Acid-Based Immune System: the Antiviral Potential of Mammalian RNA Silencing
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B. Bartel and D. P. Bartel
MicroRNAs: At the Root of Plant Development?
Plant Physiology,
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S. Bhullar, S. Chakravarthy, S. Advani, S. Datta, D. Pental, and P. K. Burma
Strategies for Development of Functionally Equivalent Promoters with Minimum Sequence Homology for Transgene Expression in Plants: cis-Elements in a Novel DNA Context versus Domain Swapping
Plant Physiology,
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A. Dillin
The specifics of small interfering RNA specificity
PNAS,
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E. Bucher, T. Sijen, P. de Haan, R. Goldbach, and M. Prins
Negative-Strand Tospoviruses and Tenuiviruses Carry a Gene for a Suppressor of Gene Silencing at Analogous Genomic Positions
J. Virol.,
December 20, 2002;
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[Abstract]
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F. Qu, T. Ren, and T. J. Morris
The Coat Protein of Turnip Crinkle Virus Suppresses Posttranscriptional Gene Silencing at an Early Initiation Step
J. Virol.,
December 6, 2002;
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E. I. Savenkov and J. P. T. Valkonen
Silencing of a viral RNA silencing suppressor in transgenic plants
J. Gen. Virol.,
September 1, 2002;
83(9):
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R. H. A. Plasterk
RNA Silencing: The Genome's Immune System
Science,
May 17, 2002;
296(5571):
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[Abstract]
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P. D. Zamore
Ancient Pathways Programmed by Small RNAs
Science,
May 17, 2002;
296(5571):
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[Abstract]
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K. Kashkush, M. Feldman, and A. A. Levy
Gene Loss, Silencing and Activation in a Newly Synthesized Wheat Allotetraploid
Genetics,
April 1, 2002;
160(4):
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[Abstract]
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M. Ruegger and C. Chapple
Mutations That Reduce Sinapoylmalate Accumulation in Arabidopsis thaliana Define Loci With Diverse Roles in Phenylpropanoid Metabolism
Genetics,
December 1, 2001;
159(4):
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[Abstract]
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R. F. Ketting, S. E.J. Fischer, E. Bernstein, T. Sijen, G. J. Hannon, and R. H.A. Plasterk
Dicer functions in RNA interference and in synthesis of small RNA involved in developmental timing in C. elegans
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October 15, 2001;
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[Abstract]
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