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Molecular Characterization ofRht-1Dwarfing Genes in Hexaploid Wheat

矮化 侏儒症 生物 基因 等位基因 遗传学 错义突变 突变体 表型
作者
Stephen Pearce,Robert Saville,Simon P. Vaughan,Peter M. Chandler,Edward P. Wilhelm,Caroline A. Sparks,Nadia Al-Kaff,Andrey Korolev,Margaret I. Boulton,Andrew L. Phillips,Peter Hedden,P. Nicholson,Stephen G. Thomas
出处
期刊:Plant Physiology [Oxford University Press]
卷期号:157 (4): 1820-1831 被引量:277
标识
DOI:10.1104/pp.111.183657
摘要

Abstract The introduction of the Reduced height (Rht)-B1b and Rht-D1b semidwarfing genes led to impressive increases in wheat (Triticum aestivum) yields during the Green Revolution. The reduction in stem elongation in varieties containing these alleles is caused by a limited response to the phytohormone gibberellin (GA), resulting in improved resistance to stem lodging and yield benefits through an increase in grain number. Rht-B1 and Rht-D1 encode DELLA proteins, which act to repress GA-responsive growth, and their mutant alleles Rht-B1b and Rht-D1b are thought to confer dwarfism by producing more active forms of these growth repressors. While no semidwarfing alleles of Rht-A1 have been identified, we show that this gene is expressed at comparable levels to the other homeologs and represents a potential target for producing novel dwarfing alleles. In this study, we have characterized additional dwarfing mutations in Rht-B1 and Rht-D1. We show that the severe dwarfism conferred by Rht-B1c is caused by an intragenic insertion, which results in an in-frame 90-bp insertion in the transcript and a predicted 30-amino acid insertion within the highly conserved amino-terminal DELLA domain. In contrast, the extreme dwarfism of Rht-D1c is due to overexpression of the semidwarfing Rht-D1b allele, caused by an increase in gene copy number. We show also that the semidwarfing alleles Rht-B1d and Rht-B1e introduce premature stop codons within the amino-terminal coding region. Yeast two-hybrid assays indicate that these newly characterized mutations in Rht-B1 and Rht-D1 confer “GA-insensitive” dwarfism by producing DELLA proteins that do not bind the GA receptor GA INSENSITIVE DWARF1, potentially compromising their targeted degradation.

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