Plant Physiol.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Plant Physiology Preview
Published on June 24, 2005; 10.1104/pp.105.063909


This Article
Right arrow Full Text (Plant Physiology Preview (PDF))
Right arrow All Versions of this Article:
138/3/1396    most recent
pp.105.063909v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Alexander, D. L.
Right arrow Articles by Langdale, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Alexander, D. L.
Right arrow Articles by Langdale, J. A.
Agricola
Right arrow Articles by Alexander, D. L.
Right arrow Articles by Langdale, J. A.

Received April 13, 2005
Returned for revision April 13, 2005
Accepted April 22, 2005

CORKSCREW1 Defines a Novel Mechanism of Domain Specification in the Maize Shoot

Debbie L. Alexander , E. Anne Mellor , and Jane A. Langdale *

Department of Plant Sciences, University of Oxford, Oxford OX1 3RB, United Kingdom

* Corresponding author; email: jane.langdale{at}plants.ox.ac.uk.

In higher plants, determinate leaf primordia arise in regular patterns on the flanks of the indeterminate shoot apical meristem (SAM). The acquisition of leaf form is then a gradual process, involving the specification and growth of distinct domains within the three leaf axes. The recessive corkscrew1 (cks1) mutation of maize (Zea mays) disrupts both leaf initiation patterns in the SAM and domain specification within the mediolateral and proximodistal leaf axes. Specifically, cks1 mutant leaves exhibit multiple midribs and leaf sheath tissue differentiates in the blade domain. Such perturbations are a common feature of maize mutants that ectopically accumulate KNOTTED1-like homeobox (KNOX) proteins in leaf tissue. Consistent with this observation, at least two knox genes are ectopically expressed in cks1 mutant leaves. However, ectopic KNOX proteins cannot be detected. We therefore propose that CKS1 primarily functions within the SAM to establish boundaries between meristematic and leaf zones. Loss of gene function disrupts boundary formation, impacts phyllotactic patterns, and leads to aspects of indeterminate growth within leaf primordia. Because these perturbations arise independently of ectopic KNOX activity, the cks1 mutation defines a novel component of the developmental machinery that facilitates leaf-versus-shoot development in maize.




This article has been cited by other articles:


Home page
Cold Spring Harb Symp Quant BiolHome page
M. Lodha, C.F. Marco, and M.C.P. Timmermans
Genetic and Epigenetic Regulation of Stem Cell Homeostasis in Plants
Cold Spring Harb Symp Quant Biol, January 15, 2009; (2009) sqb.2008.73.044v1.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 2005 by the American Society of Plant Biologists