Search bioRxivSearch

Biology subjects

Quint, M.

Publications and source records attributed to Quint, M..

2 recordsLinked to original sources

Photoperiod sensing of the circadian clock is controlled by ELF3 and GI

ELF3 and GI are two important components of the Arabidopsis circadian clock. They are not only essential for the oscillator function but are also pivotal in mediating light inputs to the oscillator. Lack of either results in a defective oscillator causing severely compromised output pathways, such as photoperiodic flowering and hypocotyl elongation. Although single loss of function mutants of ELF3 and GI have been well-studied, their genetic interaction remains unclear. We generated an elf3 gi double mutant to study their genetic relationship in clock-controlled growth and phase transition phenotypes. We found that ELF3 and GI repress growth differentially during the night and the day, respectively. Circadian clock assays revealed that ELF3 and GI are essential Zeitnehmers that enable the oscillator to synchronize the endogenous cellular mechanisms to external environmental signals. In their absence, the circadian oscillator fails to synchronize to the light-dark cycles even under diurnal conditions. Consequently, clock-mediated photoperiod-responsive growth and development is completely lost in plants lacking both genes, suggesting that ELF3 and GI together convey photoperiod sensing to the central oscillator. Since ELF3 and GI are conserved across flowering plants and represent important breeding and domestication targets, our data highlight the possibility of developing photoperiod-insensitive crops by adjusting the allelic combination of these two key genes.\n\nOne sentence summaryELF3 and GI are essential for circadian clock mediated photoperiod sensing.

plant biology

Young Genes To The Front -- A Strategy For Future Resistance Against Powdery Mildew?

Nonhost resistance of a plant against a microbial pathogen can be the result of a long-lasting coevolutionary optimization of resource allocation in both host and pathogen. Although this has been suggested for years, coevolutionary aspects leading to nonhost resistance in plants are not fully understood yet. Instead, most studies focus on limited subsets of genes which are differentially expressed in infected plants to describe details of defense strategies and symptoms of diseases.\n\nHere, we exploit publicly available whole genome gene expression data and combine them with evolutionary characteristics of genes to uncover a mechanism of host-pathogen coevolution. Our results suggest that metabolic efficiency in gene regulation is a key aspect leading to nonhost resistance. In addition, we find that progressing host-pathogen coevolution is accompanied by subtle, but systematic overexpression of recently founded genes. In support of our plant-specific data, we observe similar effects in animal species.

evolutionary biology