Access the full text.
Sign up today, get DeepDyve free for 14 days.
M. Koornneef, J. H Veen (1980)
Induction and analysis of gibberellin sensitive mutants in Arabidopsis thaliana (L.) HeynhTheor. Appl. Genet, 58
H. Klee, M Estelle (1991)
Molecular analysis of hormone mutants in higher plantsAnn. Rev. Plant Physiol. Plant Mol. Biol, 42
D. McCarty, T. Hattori, C. Carson, V. Vasil, Mark Lazar, I. Vasil (1991)
The Viviparous-1 developmental gene of maize encodes a novel transcriptional activatorCell, 66
A. Feinberg, B. Vogelstein (1983)
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.Analytical biochemistry, 132 1
G. Haughn, C. R Somerville (1986)
Sulfonylurea‐resistant mutants of Arabidopsis thalianaMol. Gen. Genet, 204
C. Robichaud, J. Wong, I. Sussex (1979)
Control of in vitro growth of viviparous embryo mutants of maize by abscisic acidDevelopmental Genetics, 1
P. Pang, R. E. Pruitt, E. M Meyerowitz (1988)
Molecular cloning, genomic organization, expression and evolution of 12S seed storage protein genes of Arabidopsis thalianaDev. Genet, 11
K. Izumi, I. Yamaguchi, A. Wada, H. Oshio, N. Takahashi (1984)
Effects of a New Plant Growth Retardant (E)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol (S-3307) on the Growth and Gibberellin Content of Rice PlantsPlant and Cell Physiology, 25
D. McCarty, C. Carson, P. Stinard, Donald Robertson (1989)
Molecular Analysis of viviparous-1: An Abscisic Acid-Insensitive Mutant of Maize.The Plant cell, 1
S. Naito, P. H. Dube, R. N Beachy (1988)
Differential expression of conglycinin a' and b subunit genes in transgenic plantsPlant Physiol, 11
G. Galau, K. Jakobsen, D. Hughes (1991)
The controls of late dicot embryogenesis and early germinationPhysiologia Plantarum, 81
E. Nambara, Takashi Akazawa, Peter McCourt (1991)
Effects of the gibberellin biosynthetic inhibitor uniconazol on mutants of Arabidopsis.Plant physiology, 97 2
H. Klee, M. Estelle (1991)
Molecular Genetic Approaches to Plant Hormone Biology, 42
M. Koornneef, M. L. Jorna, D. L. C. Brinkhorst‐van der Swan, C. M Karssen (1982)
The isolation of abscisic acid (ABA)‐deficient mutants by selection of induced revertants in nongerminating gibberellin‐sensitive lines of Arabidopsis (L.) HeynhTheor. Appl. Genet, 61
Philippe Guerche, agl Tire, Fatima Sa, A. Clercq, M. Montagu, Enno Krebbersas (1990)
Differential Expression of the Arabidopsis 2S Albumin Genes and the Effect of Increasing Gene Family Size.The Plant cell, 2
M. Ashburner (1989)
A Laboratory manual
J. D. Heath, R. Weldon, R. Monnot, D. W Meinke (1986)
Analysis of storage proteins in normal and aborted seeds from embryo‐lethal mutants of Arabidopsis thalianaPlanta, 169
G. Galau, Niddhi Bijaisoradat, D. Hughes (1987)
Accumulation kinetics of cotton late embryogenesis-abundant mRNAs and storage protein mRNAs: coordinate regulation during embryogenesis and the role of abscisic acid.Developmental biology, 123 1
S. J. Neill, R. Horgan, A. F Rees (1987)
Seed development and vivipary in Zea mays LPlant Mol. Biol, 171
M. Koornneef, G. Reuling, C. Karssen (1984)
The isolation and characterization of abscisic acid-insensitive mutants of Arabidopsis thalianaPhysiologia Plantarum, 61
C. M. Karssen, D. L. C. Brinkhorst‐van der Swan, A. E. Breekland, M Koornnef (1983)
Induction of dormancy during seed development by endogenous abscisic acid: studies on abscisic acid: studies on abscisic acid deficient genotypes of Arabidopsis thaliana (L.) HeynhPlanta, 157
Maarten Koornneef, C. Hanhart, H. Hilhorst, C. Karssen (1989)
In Vivo Inhibition of Seed Development and Reserve Protein Accumulation in Recombinants of Abscisic Acid Biosynthesis and Responsiveness Mutants in Arabidopsis thaliana.Plant physiology, 90 2
L. Dure, M. Crouch, J. Harada, T.‐H. D. Ho, J. Mundy, R. Quatrano, T. Thomas, Z. R Sung (1989)
Common amino acid sequence domains among the LEA proteins of higher plantsPlant Mol. Biol., 12
In order to investigate the role of the plant hormones gibberellin (GA) and abscisic acid (ABA) in seed development and germination the GA biosynthetic inhibitor, Uniconazol, was used to isolate mutants with abnormal germination profiles. In one of these mutants, the ability to germinate on Uniconazol is due to a mutation in the ABI3 gene. However, unlike the previously reported abi3 mutant, this line displays an array of seed‐specific developmental defects. The accumulation of seed reserve proteins is dramatically reduced due to reduced levels of the storage protein mRNA. The embryos remain green throughout development and are desiccation intolerant. However, immature seeds are completely non‐dormant and grow normally. These results suggest the ABI3 gene is essential for the synthesis of seed storage proteins and for the protection of the embryo during desiccation.
The Plant Journal – Wiley
Published: Jul 1, 1992
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.