Abstract
The maize (Zea mays) CRINKLY4 (cr4) gene encodes a receptor-like kinase that controls a variety of cell differentiation responses, particularly in the leaf epidermis and in the aleurone of the endosperm. In situ hybridization indicated that the cr4 transcript is present throughout the shoot apical meristem and young leaf primordia. A genetic mosaic analysis was conducted to test whether CR4 signal transduction directly regulated the cellular processes associated with differentiation or whether differentiation was controlled through the production of a secondary signal. Genetic mosaics were created using gamma-rays to induce chromosome breakage in a cr4/Cr4+ heterozygote. The mutant cr4 allele was marked with the albino mutation, Oy-700. Breakage and loss of the chromosome arm carrying the wild-type alleles created a sector of albino, cr4 mutant tissue in an otherwise normal leaf. Analysis of such sectors indicated that cr4 functions cell autonomously to regulate cell morphogenesis, implying that CR4 signal transduction regulates cell differentiation through strictly intracellular functions and not the production of secondary intercellular signals. However, several sectors altered cell patterning in wild-type tissue adjacent to the sectors, suggesting that cr4 mutant cells are defective in the production of other lateral signals.
MeSH Terms
Anthocyanins/metabolism
Cell Differentiation
Chromosome Breakage
Gamma Rays
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Plant
Genetic Markers
In Situ Hybridization
Mutation
Phenotype
Plant Epidermis/genetics,growth & development,ultrastructure
Plant Proteins
Plant Shoots/genetics,growth & development,ultrastructure
Protein Kinases/genetics,physiology
Signal Transduction
Zea mays/enzymology,genetics,growth & development
Chemicals
Anthocyanins
Genetic Markers
Plant Proteins
Protein Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Becraft P W
Zoology and Genetics/Agronomy Departments, 2116 Molecular Biology Building, Iowa State University, Ames, IA 50011, USA.
[email protected]
Kang S H
Suh S G
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