Literature DB >> 11041880

A leaf-derived signal is a quantitative determinant of floral form in Impatiens.

F Tooke1, N H Battey.   

Abstract

The completion of flower development in Impatiens balsamina requires continuous inductive (short-day) conditions. We have previously shown that a leaf-derived signal has a role in floral maintenance. The research described here analyzes the role of the leaf in flower development. Leaf removal treatments, in which plants were restricted to a specified number of leaves, resulted in flowers with increased petal number, up to double that of the undefoliated control. Similar petal number increases (as well as changes in bract number or morphology) were recorded when plants began their inductive treatment at a late developmental age or when plants of a nonreverting line (capable of floral maintenance in the absence of continuous short days) were transferred from short days to long days. Our data imply that the increased petal number was neither a response to stress effects associated with leaf removal nor a result of alterations in primordium initiation rates or substitutions of petals for stamens. Rather, the petal initiation phase was prolonged when the amounts of a leaf-derived signal were limiting. We conclude that a leaf-derived signal has a continuous and quantitative role in flower development and propose a temporal model for the action of organ identity genes in Impatiens. This work adds a new dimension to the prevailing ABC model of flower development and may provide an explanation for the wide variety and instabilities of floral form seen among certain species in nature.

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Mesh:

Year:  2000        PMID: 11041880      PMCID: PMC149123          DOI: 10.1105/tpc.12.10.1837

Source DB:  PubMed          Journal:  Plant Cell        ISSN: 1040-4651            Impact factor:   11.277


  27 in total

1.  Integration of floral inductive signals in Arabidopsis.

Authors:  M A Blázquez; D Weigel
Journal:  Nature       Date:  2000-04-20       Impact factor: 49.962

Review 2.  Three ways to learn the ABCs.

Authors:  M Ng; M F Yanofsky
Journal:  Curr Opin Plant Biol       Date:  2000-02       Impact factor: 7.834

3.  The protein encoded by the Arabidopsis homeotic gene agamous resembles transcription factors.

Authors:  M F Yanofsky; H Ma; J L Bowman; G N Drews; K A Feldmann; E M Meyerowitz
Journal:  Nature       Date:  1990-07-05       Impact factor: 49.962

4.  Flowers into shoots: photo and hormonal control of a meristem identity switch in Arabidopsis.

Authors:  J K Okamuro; B G den Boer; C Lotys-Prass; W Szeto; K D Jofuku
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-26       Impact factor: 11.205

5.  FON1, an Arabidopsis gene that terminates floral meristem activity and controls flower organ number.

Authors:  H Huang; H Ma
Journal:  Plant Cell       Date:  1997-02       Impact factor: 11.277

6.  Control of floral homeotic gene expression and organ morphogenesis in Antirrhinum.

Authors:  P C McSteen; C A Vincent; S Doyle; R Carpenter; E S Coen
Journal:  Development       Date:  1998-07       Impact factor: 6.868

7.  Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum.

Authors:  D Bradley; R Carpenter; H Sommer; N Hartley; E Coen
Journal:  Cell       Date:  1993-01-15       Impact factor: 41.582

8.  ETTIN patterns the Arabidopsis floral meristem and reproductive organs.

Authors:  A Sessions; J L Nemhauser; A McColl; J L Roe; K A Feldmann; P C Zambryski
Journal:  Development       Date:  1997-11       Impact factor: 6.868

9.  CLAVATA1, a regulator of meristem and flower development in Arabidopsis.

Authors:  S E Clark; M P Running; E M Meyerowitz
Journal:  Development       Date:  1993-10       Impact factor: 6.868

10.  Mutations in the PERIANTHIA gene of Arabidopsis specifically alter floral organ number and initiation pattern.

Authors:  M P Running; E M Meyerowitz
Journal:  Development       Date:  1996-04       Impact factor: 6.868

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  7 in total

1.  Leaf-to-shoot apex movement of symplastic tracer is restricted coincident with flowering in Arabidopsis.

Authors:  Andreas Gisel; Frederick D Hempel; Sandra Barella; Patricia Zambryski
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-29       Impact factor: 11.205

Review 2.  Aspects of plant intelligence.

Authors:  Anthony Trewavas
Journal:  Ann Bot       Date:  2003-05-09       Impact factor: 4.357

Review 3.  Floral meristem initiation and emergence in plants.

Authors:  J W Chandler
Journal:  Cell Mol Life Sci       Date:  2012-05-10       Impact factor: 9.261

4.  Polycomb-Group Proteins and FLOWERING LOCUS T Maintain Commitment to Flowering in Arabidopsis thaliana.

Authors:  Ralf Müller-Xing; Oliver Clarenz; Lena Pokorny; Justin Goodrich; Daniel Schubert
Journal:  Plant Cell       Date:  2014-06-10       Impact factor: 11.277

5.  Floral Reversion in Arabidopsis suecica Is Correlated with the Onset of Flowering and Meristem Transitioning.

Authors:  Amelia Asbe; Starr C Matsushita; Spencer Gordon; H E Kirkpatrick; Andreas Madlung
Journal:  PLoS One       Date:  2015-05-26       Impact factor: 3.240

6.  Deeper Insight into the Volatile Profile of Rosa willmottiae with Headspace Solid-Phase Microextraction and GC-MS Analysis.

Authors:  Ruifang Jiao; Ping Gao; Xinfen Gao
Journal:  Molecules       Date:  2022-02-12       Impact factor: 4.411

7.  SMRT and Illumina RNA-Seq Identifies Potential Candidate Genes Related to the Double Flower Phenotype and Unveils SsAP2 as a Key Regulator of the Double-Flower Trait in Sagittaria sagittifolia.

Authors:  Meiping Gao; Wen Jiang; Zhicheng Lin; Qian Lin; Qinghua Ye; Wei Wang; Qian Xie; Xinhua He; Cong Luo; Qingxi Chen
Journal:  Int J Mol Sci       Date:  2022-02-17       Impact factor: 5.923

  7 in total

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