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The dicer-like1 Homolog fuzzy tassel Is Required for the Regulation of Meristem Determinacy in the Inflorescence and Vegetative Growth in Maize
Authors:Beth E Thompson  Christine Basham  Reza Hammond  Queying Ding  Atul Kakrana  Tzuu-Fen Lee  Stacey A Simon  Robert Meeley  Blake C Meyers  Sarah Hake
Institution:aDepartment of Biology, East Carolina University, Greenville, North Carolina 27858;bCenter for Bioinformatics and Computational Biology, University of Delaware, Newark, Delaware 19714;cDepartment of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19711;dPioneer, A Dupont Company, Johnston, Iowa 50131;ePlant Gene Expression Center and University of California-Berkeley, Albany, California 94710
Abstract:Plant architecture is determined by meristems that initiate leaves during vegetative development and flowers during reproductive development. Maize (Zea mays) inflorescences are patterned by a series of branching events, culminating in floral meristems that produce sexual organs. The maize fuzzy tassel (fzt) mutant has striking inflorescence defects with indeterminate meristems, fasciation, and alterations in sex determination. fzt plants have dramatically reduced plant height and shorter, narrower leaves with leaf polarity and phase change defects. We positionally cloned fzt and discovered that it contains a mutation in a dicer-like1 homolog, a key enzyme required for microRNA (miRNA) biogenesis. miRNAs are small noncoding RNAs that reduce target mRNA levels and are key regulators of plant development and physiology. Small RNA sequencing analysis showed that most miRNAs are moderately reduced in fzt plants and a few miRNAs are dramatically reduced. Some aspects of the fzt phenotype can be explained by reduced levels of known miRNAs, including miRNAs that influence meristem determinacy, phase change, and leaf polarity. miRNAs responsible for other aspects of the fzt phenotype are unknown and likely to be those miRNAs most severely reduced in fzt mutants. The fzt mutation provides a tool to link specific miRNAs and targets to discrete phenotypes and developmental roles.
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