Access the full text.
Sign up today, get DeepDyve free for 14 days.
P. Polowick, V. Sawhney (1986)
A SCANNING ELECTRON MICROSCOPIC STUDY ON THE INITIATION AND DEVELOPMENT OF FLORAL ORGANS OF BRASSICA NAPUS (CV. WESTAR)American Journal of Botany, 73
A. Nelson
The inheritance of sex in an abnormal (Carpellodic)wall-flower
A. Bennett (1870)
Vegetable Teratology : An Account of the Principal Deviations from the usual Construction of PlantsNature, 1
(1963)
Sex expression in flowering plants
M. Komaki, K. Okada, Eisho Shino, Yoshiro Shimura (1988)
Isolation and characterization of novel mutants of Arabidopsis thaliana defective in flower developmentDevelopment, 104
(1971)
Uber eine Rbntgenmutante von Arabidopsis thaliana (L.) Heynh. mit ver&ndertem Bletenbau und Bletenstand
(1961)
Zur Charakterisierung der Bitten und Infloreszenzen von Arabidopsis tha/iana (L
A. Arber (1931)
STUDIES IN FLORAL MORPHOLOGYNew Phytologist, 30
E. Lewis (1978)
A gene complex controlling segmentation in DrosophilaNature, 276
(1929)
Species hybridization among old and new species of shepherd's purse
M. Koornneef, J. Cone, C. Karssen, R. Kendrick, J. Veen, J. Zeevaart (1985)
Plant hormone and photoreceptor mutants of Arabidopsis and tomato
(1955)
The morphology and growth of the vegetative and reproductive apices of Arabidopsis tha/iana
V. Sawhney, R. Greyson (1973)
Morphogenesis of the stamenless-2 mutant in tomato. II. Modifications of sex organs in the mutant and normal flowers by plant hormonesBotany, 51
M. Koornneef, J. Vaneden, Cj Hanhart, P. Stam, F. Braaksma, W. Feenstra (1983)
Linkage map of Arabidopsis thalianaJournal of Heredity, 74
M. Scott, S. Carroll (1987)
The segmentation and homeotic gene network in early Drosophila developmentCell, 51
M. Masters
Vegetable Teratology: An Account of the Principal Deviations from the Usual Construction of Plants
M. Masters (1875)
Double FlowersNature, 27
(1988)
A dominant mutation confers insensitivity to ethylene in Arabidopsis tha/iana
(1973)
The inheritance of apetalous flower type in Petunia hybrida Vilm
(1988)
Arabidopsis thaliana : A review
(1919)
Erblichkeitsversuche mit einer dekandrischen Capsella bursa pastoris (L.). Svensk Bot
F. Brieger (1935)
The developmental mechanics of normal and abnormal flowers in Primula, 147
Alan Hughen (1980)
The Regulation of Tobacco Floral Organ InitiationBotanical Gazette, 141
M. Koornneef, J. Bruin, P. Goettsch (1980)
A provisional map of chromosome 4 of Arahidopsis, 17
Capse//a bursa-pastoris (L.) Medic., and Anagal/is arvensis L
Renner Botanisches (1959)
Somatic conversion in the heredity of the Cruciata character in ŒnotheraHeredity, 13
(1951)
Taxonomy of Vascular Rants
J. Payer
Traité d'organogénie comparée de la fleur
P. King (1988)
Plant hormone mutants.Trends in genetics : TIG, 4 6
(1965)
Flower malformations in mutants as a means of partitioning the developmental process
G. Haughn, C. Somerville (1988)
Genetic control of morphogenesis in ArabidopsisDevelopmental Genetics, 9
(1987)
Molecular genetics and development of Arabidopsis
W. Bateson (1910)
Mendel's Principles of HeredityThe Indian Medical Gazette, 45
M. Akam (1987)
The molecular basis for metameric pattern in the Drosophila embryo.Development, 101 1
Soc. Dev. Biol
Abstract We describe the effects of four recessive homeotic mutations that specifically disrupt the development of flowers in Arabidopsis thaliana. Each of the recessive mutations affects the outcome of organ development, but not the location of organ primordia. Homeotic transformations observed are as follows. In agamous-1, stamens to petals; in apetala2-1, sepals to leaves and petals to staminoid petals; in apetala3-1, petals to sepals and stamens to carpels; in pistillata-1, petals to sepals. In addition, two of these mutations (ap2-1 and pi-1) result in loss of organs, and ag-1 causes the cells that would ordinarily form the gynoecium to differentiate as a flower. Two of the mutations are temperature-sensitive. Temperature shift experiments indicate that the wild-type AP2 gene product acts at the time of primordium initiation; the AP3 product is active later. It seems that the wild-type alleles of these four genes allow cells to determine their place in the developing flower and thus to differentiate appropriately. We propose that these genes may be involved in setting up or responding to concentric, overlapping fields within the flower primordium. This content is only available as a PDF. © 1989 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
The Plant Cell – Oxford University Press
Published: Jan 1, 1989
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.