RESUMO
To survive and thrive in a dynamic environment, plants must continuously monitor their surroundings and adjust their development and physiology accordingly. Changes in gene expression underlie these developmental and physiological adjustments, and are traditionally attributed to widespread transcriptional reprogramming. Growing evidence, however, suggests that post-transcriptional mechanisms also play a vital role in tailoring gene expression to a plant's environment. Untranslated regions (UTRs) act as regulatory hubs for post-transcriptional control, harbouring cis-elements that affect an mRNA's processing, localization, translation, and stability, and thereby tune the abundance of the encoded protein. Here, we review recent advances made in understanding the critical function UTRs exert in the post-transcriptional control of gene expression in the context of a plant's abiotic environment. We summarize the molecular mechanisms at play, present examples of UTR-controlled signalling cascades, and discuss the potential that resides within UTRs to render plants more resilient to a changing climate.
Assuntos
Regulação da Expressão Gênica de Plantas , Regiões não Traduzidas , Plantas/genética , Plantas/metabolismo , Meio AmbienteRESUMO
Phytohormones act as key regulators of plant growth that coordinate developmental and physiological processes across cells, tissues and organs. As such, their levels and distribution are highly dynamic owing to changes in their biosynthesis, transport, modification and degradation that occur over space and time. Fluorescent biosensors represent ideal tools to track these dynamics with high spatiotemporal resolution in a minimally invasive manner. Substantial progress has been made in generating a diverse set of hormone sensors with recent FRET biosensors for visualising hormone concentrations complementing information provided by transcriptional, translational and degron-based reporters. In this review, we provide an update on fluorescent biosensor designs, examine the key properties that constitute an ideal hormone biosensor, discuss the use of these sensors in conjunction with in vivo hormone perturbations and highlight the latest discoveries made using these tools.
Assuntos
Técnicas Biossensoriais/métodos , Corantes Fluorescentes , Reguladores de Crescimento de Plantas/metabolismo , Plantas/metabolismo , Engenharia Genética , Células Vegetais , Plantas/genéticaAssuntos
Brassinosteroides , MicroRNAs , Reguladores de Crescimento de Plantas , Transdução de Sinais , MicroRNAs/genética , MicroRNAs/metabolismo , Brassinosteroides/metabolismo , Reguladores de Crescimento de Plantas/metabolismo , Regulação da Expressão Gênica de Plantas , Arabidopsis/genética , Arabidopsis/metabolismo , RNA de Plantas/genética , RNA de Plantas/metabolismoAssuntos
Estômatos de Plantas , Estômatos de Plantas/citologia , Estômatos de Plantas/fisiologia , Estômatos de Plantas/genética , Estômatos de Plantas/metabolismo , Anisotropia , Arabidopsis/citologia , Arabidopsis/fisiologia , Arabidopsis/genética , Arabidopsis/metabolismo , Arabidopsis/crescimento & desenvolvimentoRESUMO
Plant development displays a remarkable degree of plasticity and continuously adjusts to the plant's surroundings, a process that is triggered by the perception of environmental cues such as light and temperature. Transcription factors of the PHYTOCHROME-INTERACTING FACTOR (PIF) family have long been established as key negative regulators of light responses; within the last decade, increasing evidence suggests that they are also core components of temperature signalling, and multiple mechanisms by which temperature regulates activity of these transcription factors have been discovered. It has become clear that these temperature responses cannot be considered in isolation, but that they occur in the context of, and are influenced by, other environmental signals. This review discusses recent advances in the understanding of the mechanisms through which temperature affects PIF function and how these mechanisms are influenced by the light environment.
Assuntos
Proteínas de Arabidopsis , Arabidopsis , Fitocromo , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Regulação da Expressão Gênica de Plantas , Transdução de Sinais , TemperaturaRESUMO
The Arabidopsis (Arabidopsis thaliana) COP1/SPA ubiquitin ligase is a central repressor that suppresses light signaling in darkness by targeting positive regulators of the light response, mainly transcription factors, for degradation. Light inactivates COP1/SPA, in part by excluding COP1 from the nucleus. SPA proteins are essential cofactors of COP1, but their exact role in the COP1/SPA complex is thus far unknown. To unravel a potential role of SPA proteins in COP1 nucleocytoplasmic partitioning, we monitored the subcellular localization of COP1 in a spa1234 quadruple mutant (spaQn). We analyzed a YFP-COP1-expressing transgenic line and endogenous COP1 after subcellular fractionation. In dark-grown seedlings, both YFP-COP1 and endogenous COP1 accumulated in the nucleus in the absence and presence of SPA proteins, indicating that SPA proteins are not required for nuclear localization of COP1 in darkness. In contrast, in white light-grown seedlings, spaQn mutants failed to relocalize COP1 from the nucleus to the cytoplasm. Hence, SPA proteins are necessary for the light-controlled change in COP1 subcellular localization. We conclude that SPA proteins have a dual role: (1) they are required for light-responsiveness of COP1 subcellular localization, and (2) they promote COP1 activity in darkness in a fashion that is independent of the nuclear import/nuclear retention of COP1.
Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis/metabolismo , Arabidopsis/efeitos da radiação , Luz , Morfogênese/efeitos da radiação , Ubiquitina-Proteína Ligases/metabolismo , Núcleo Celular/metabolismo , Escuridão , Mutação/genética , Transporte Proteico/efeitos da radiação , Plântula/crescimento & desenvolvimento , Plântula/metabolismo , Plântula/efeitos da radiação , Frações Subcelulares/metabolismoRESUMO
Stomatal development is tightly regulated through internal and external factors that are integrated by a complex signalling network. Light represents an external factor that strongly promotes stomata formation. Here, we show that auxin-resistant aux/iaa mutants, e.g. axr3-1, exhibit a de-repression of stomata differentiation in dark-grown seedlings. The higher stomatal index in dark-grown axr3-1 mutants when compared with the wild type is due to increased cell division in the stomatal lineage. Excessive stomata in dark-grown seedlings were also observed in mutants defective in auxin biosynthesis or auxin perception and in seedlings treated with the polar auxin transport inhibitor NPA. Consistent with these findings, exogenous auxin repressed stomata formation in light-grown seedlings. Taken together, these results indicate that auxin is a negative regulator of stomatal development in dark-grown seedlings. Epistasis analysis revealed that axr3-1 acts genetically upstream of the bHLH transcription factors SPCH, MUTE and FAMA, as well as the YDA MAP kinase cascade, but in parallel with the repressor of photomorphogenesis COP1 and the receptor-like protein TMM. The effect of exogenous auxin required the ER family of leucine-rich repeat receptor-like kinases, suggesting that auxin acts at least in part through the ER family. Expression of axr3-1 in the stomatal lineage was insufficient to alter the stomatal index, implying that cell-cell communication is necessary to mediate the effect of auxin. In summary, our results show that auxin signalling contributes to the suppression of stomatal differentiation observed in dark-grown seedlings.