IFEVA   02662
INSTITUTO DE INVESTIGACIONES FISIOLOGICAS Y ECOLOGICAS VINCULADAS A LA AGRICULTURA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Rol de las argininmetiltransferasas en el control de las respuestas foromorfogénicas y los ritmos circadianos en plantas
Autor/es:
SANCHEZ, S; HERNANDO, E; RUGNONE, M; CERDAN, P; BECKWITH, E; CERIANI, MF; MAS, P; YANOVSKY, M
Lugar:
Rosario
Reunión:
Congreso; Reunión Argentina de Fisiología Vegetal; 2008
Institución organizadora:
Sociedad Argentina de Fisiología Vegetal
Resumen:
Interlocked transcriptional feed-back loops are the basis of circadian oscillations in many organisms. In Arabidopsis these loops involve the Myb transcription factors CCA1 and LHY, and the pseudo-response regulators (PRRs) TOC1, PRR3, PRR5, PRR7 and PRR9. Using a forward genetic approach, we identified protein arginine methyltransferase 5 (PRMT5) as a key regulator of clock function and light signaling. prmt5 mutants show increased period length of circadian rhythms and reduced photomorphogenic responses to red, far-red and blue light suggesting that PRMT5 mediates light regulation of the circadian clock. prmt5 mutants flower very late under long and short day conditions due to an enhanced expression of the MADS box transcription factor FLC. Although FLC has been shown to regulate clock function, flc mutation suppresses the late flowering phenotype of prmt5 mutants but has no effect on its circadian phenotype. PRMT5 methylates histone and non-histone proteins, and regulates transcription, RNA processing, and signal transduction in many eukaryotic organisms. To further understand the mechanisms of PRTM5 action in plants we compared the prmt5 transcriptome with that of wild type plants using Affymetrix microarrays. The gene showing the highest enhancement in expression was PRR9, a key component of the Arabidopsis circadian oscillator, whose expression is also acutely regulated by light. Our results uncover a role for arginine methylation in clock regulation in Arabidopsis, presumably through the direct or indirect regulation of the PRR9 clock gene.