The novel quantitative trait locus GL3.1 controls rice grain size and yield by regulating Cyclin-T1;3
Increased crop yields are required to support rapid population growth worldwide. Grain weight is a key compo- nent of rice yield, but the underlying molecular mechanisms that control it remain elusive. Here, we report the clon- ing and characterization of a new quantitative trait locus (QTL) for the...
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Veröffentlicht in: | Cell research 2012-12, Vol.22 (12), p.1666-1680 |
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Sprache: | eng |
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Zusammenfassung: | Increased crop yields are required to support rapid population growth worldwide. Grain weight is a key compo- nent of rice yield, but the underlying molecular mechanisms that control it remain elusive. Here, we report the clon- ing and characterization of a new quantitative trait locus (QTL) for the control of rice grain length, weight and yield. This locus, GL3.1, encodes a protein phosphatase kelch (PPKL) family -- Ser/Thr phosphatase. GL3.1 is a member of the large grain WY3 variety, which is associated with weaker dephosphorylation activity than the small grain FAZ1 variety. GL3.I-WY3 influences protein phosphorylation in the spikelet to accelerate cell division, thereby re- suiting in longer grains and higher yields. Further studies have shown that GL3.1 directly dephosphorylates its sub- strate, Cyclin-TI;3, which has only been rarely studied in plants. The downregulation of Cyclin-T1;3 in rice resulted in a shorter grain, which indicates a novel function for Cyclin-T in cell cycle regulation. Our findings suggest a new mechanism for the regulation of grain size and yield that is driven through a novel phosphatase-mediated process that affects the phosphorylation of Cyclin-T1;3 during cell cycle progression, and thus provide new insight into the mechanisms underlying crop seed development. We bred a new variety containing the natural GL3.1 allele that demonstrated increased grain yield, which indicates that GL3.1 is a powerful tool for breeding high-yield crops. |
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ISSN: | 1001-0602 1748-7838 |
DOI: | 10.1038/cr.2012.151 |