Document Detail

Expression of pattern in plants: combining molecular and calculus-based biophysical paradigms.
MedLine Citation:
PMID:  10449383     Owner:  NLM     Status:  In-Data-Review    
Pattern formation in plant meristems occurs across a broad scale. At the topographical level (large scale), tissue folding in the meristem is responsible for the initiation of new organs in specific phyllotactic patterns and also determines organ shape. At the cellular level (small scale), oriented cell division and microtubule-based cellulose reinforcement control cell pattern and growth direction. I argue here that structural specification at each scale is highly efficient if the pertinent gene activity is manifested in two complementary biophysical categories. At large scale, one category is the tendency of the formative tissue to fold with a certain spatial periodicity determined by its material properties (e.g., bending stiffness from cellulose content). This latent tendency is formalized in a differential equation for physical buckling. The second category at this scale comprises boundary conditions that specify how the latent tendency is manifested as topography: whether tissue humps occur as whorls or Fibonacci spirals. This versatile combinatorial format accounts for the relative stability of alternative organ patterning as well as alternative organ shaping (e.g., stamens vs. carpels). It also accounts for the structural shifts seen in normal development and after mutation or chemical/physical intervention. At small scale, the latent differential activity is the tendency for groups of dividing cells to co-align their cytoskeletons. The curvature of the surface opposes this tendency. The least curved part of a new primordium is its quasicylindrical midportion. There, by aligning microtubules and cellulose coherently around the organ, a new growth direction is set. Thus large-scale buckling produces curvature variation, which, in turn, affects the localization and orientation of the cytoskeleton. This scheme for the coherent production of diverse geometrical features, involving calculus at two structural levels, is supported by complex organogenetic responses to simple physical intervention. Also, many morphological alternatives, wild type vs. mutant, reflect single changes in parameters in this differential-integral format.
P B Green
Related Documents :
21604353 - Biological activity of natural phytoecdysteroids from ajuga iva against the sweetpotato...
19836293 - The intracellular transport of transporters: membrane trafficking of mineral transporters.
12700763 - Amino-acid cycling drives nitrogen fixation in the legume-rhizobium symbiosis.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  American journal of botany     Volume:  86     ISSN:  0002-9122     ISO Abbreviation:  Am. J. Bot.     Publication Date:  1999 Aug 
Date Detail:
Created Date:  2011-06-17     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0370467     Medline TA:  Am J Bot     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1059-76     Citation Subset:  -    
Department of Biological Sciences, Stanford University, Stanford, California 94305.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Tertiary templates for the design of diiron proteins.
Next Document:  Why Canny's theory doesn't hold water.