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Review
. 2008;177(3):589-607.
doi: 10.1111/j.1469-8137.2007.02324.x.

Genes for control of plant stature and form

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Free article
Review

Genes for control of plant stature and form

Victor B Busov et al. New Phytol. 2008.
Free article

Abstract

Here we summarize progress in identification of three classes of genes useful for control of plant architecture: those affecting hormone metabolism and signaling; transcription and other regulatory factors; and the cell cycle. We focus on strong modifiers of stature and form that may be useful for directed modification of plant architecture, rather than the detailed mechanisms of gene action. Gibberellin (GA) metabolic and response genes are particularly attractive targets for manipulation because many act in a dose-dependent manner; similar phenotypic effects can be readily achieved in heterologous species; and induced pleiotropic effects--such as on nitrogen assimilation, photosynthesis, and lateral root production--are usually positive with respect to crop performance. Genes encoding transcription factors represent strong candidates for manipulation of plant architecture. For example, AINTEGUMENTA, ARGOS (auxin-regulated gene controlling organ size), and growth-regulating factors (GRFs) are strong modifiers of leaf and/or flower size. Plants overexpressing these genes had increased organ size and did not display negative pleiotropic effects in glasshouse environments. TCP-domain genes such as CINCINNATA, and the associated regulatory miRNAs such as miRJAW, may provide useful means to modulate leaf curvature and other foliage properties. There are considerable opportunities for comparative and translational genomics in nonmodel plant systems.

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References

    1. Abel S, Theologis A. 1996. Early genes and auxin action. Plant Physiology 111: 9-17.
    1. Aguilar-Martinez JA, Poza-Carrion C, Cubas P. 2007. Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds. Plant Cell 19: 458-472.
    1. Alonso-Blanco C, Koorneef M. 2000. Naturally occurring variation in Arabidopsis: an underexploited resource for plant genetics. Trends in Plant Science 5: 1360-1385.
    1. Amador V, Monte E, Garcia-Martinez JL, Prat S. 2001. Gibberellins signal nuclear import of PHOR1, a photoperiod-responsive protein with homology to Drosophila armadillo. Cell 106: 343-354.
    1. Anastasiou E, Lenhard M. 2007. Growing up to one's standard. Current Opinion in Plant Biology 10: 63-69.

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