Gillmor C Stewart, Silva-Ortega Claudia O, Willmann Matthew R, Buendía-Monreal Manuel, Poethig R Scott
Laboratorio Nacional de Genómica para la Biodiversidad (Langebio), Unidad de Genómica Avanzada, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Irapuato, Guanajuato, 36821, Mexico Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA
Laboratorio Nacional de Genómica para la Biodiversidad (Langebio), Unidad de Genómica Avanzada, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Irapuato, Guanajuato, 36821, Mexico.
Development. 2014 Dec;141(23):4580-9. doi: 10.1242/dev.111229. Epub 2014 Nov 5.
Temporal coordination of developmental programs is necessary for normal ontogeny, but the mechanism by which this is accomplished is still poorly understood. We have previously shown that two components of the Mediator CDK8 module encoded by CENTER CITY (CCT; Arabidopsis MED12) and GRAND CENTRAL (GCT; Arabidopsis MED13) are required for timing of pattern formation during embryogenesis. A morphological, molecular and genomic analysis of the post-embryonic phenotype of gct and cct mutants demonstrated that these genes also promote at least three subsequent developmental transitions: germination, vegetative phase change, and flowering. Genetic and molecular analyses indicate that GCT and CCT operate in parallel to gibberellic acid, a phytohormone known to regulate these same three transitions. We demonstrate that the delay in vegetative phase change in gct and cct is largely due to overexpression of miR156, and that the delay in flowering is due in part to upregulation of FLC. Thus, GCT and CCT coordinate vegetative and floral transitions by repressing the repressors miR156 and FLC. Our results suggest that MED12 and MED13 act as global regulators of developmental timing by fine-tuning the expression of temporal regulatory genes.
发育程序的时间协调对于正常个体发育是必要的,但其实现机制仍知之甚少。我们之前已经表明,由CENTER CITY(CCT;拟南芥MED12)和GRAND CENTRAL(GCT;拟南芥MED13)编码的中介体CDK8模块的两个组件是胚胎发生期间模式形成时间所必需的。对gct和cct突变体胚胎后代表型的形态学、分子和基因组分析表明,这些基因还促进至少三个后续发育转变:萌发、营养阶段转变和开花。遗传和分子分析表明,GCT和CCT与赤霉素平行作用,赤霉素是一种已知调节这相同三个转变的植物激素。我们证明,gct和cct中营养阶段转变的延迟很大程度上是由于miR156的过表达,而开花延迟部分是由于FLC的上调。因此,GCT和CCT通过抑制miR156和FLC这些阻遏物来协调营养和花的转变。我们的结果表明,MED12和MED13通过微调时间调节基因的表达,作为发育时间的全局调节因子。