Conserved genetic determinant of motor organ identity in Medicago truncatula and related legumes
Conserved genetic determinant of motor organ identity in Medicago truncatula and related legumes
Plants exhibit various kinds of movements that have fascinated scientists and the public for centuries. Physiological studies in plants with the so-called motor organ or pulvinus suggest that cells at opposite sides of the pulvinus mediate leaf or leaflet movements by swelling and shrinking. How motor organ identity is determined is unknown. Using a genetic approach, we isolated a mutant designated elongated petiolule1 ( elp1 ) from Medicago truncatula that fails to fold its leaflets in the dark due to loss of motor organs. Map-based cloning indicated that ELP1 encodes a putative plant-specific LOB domain transcription factor. RNA in situ analysis revealed that ELP1 is expressed in primordial cells that give rise to the motor organ. Ectopic expression of ELP1 resulted in dwarf plants with petioles and rachises reduced in length, and the epidermal cells gained characteristics of motor organ epidermal cells. By identifying ELP1 orthologs from other legume species, namely pea ( Pisum sativum ) and Lotus japonicus , we show that this motor organ identity is regulated by a conserved molecular mechanism.
- John Innes Centre United Kingdom
- National Institutes of Natural Sciences Japan
- Biotechnology and Biological Sciences Research Council United Kingdom
- Aberystwyth University United Kingdom
- National Institute for Basic Biology Japan
DNA, Complementary, Base Sequence, Movement, Molecular Sequence Data, Chromosome Mapping, Sequence Analysis, DNA, Genes, Plant, Real-Time Polymerase Chain Reaction, Species Specificity, Medicago truncatula, Microscopy, Electron, Scanning, Pulvinus, Cloning, Molecular, In Situ Hybridization, Transcription Factors
DNA, Complementary, Base Sequence, Movement, Molecular Sequence Data, Chromosome Mapping, Sequence Analysis, DNA, Genes, Plant, Real-Time Polymerase Chain Reaction, Species Specificity, Medicago truncatula, Microscopy, Electron, Scanning, Pulvinus, Cloning, Molecular, In Situ Hybridization, Transcription Factors
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