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Flint, A.

Publications and source records attributed to Flint, A..

3 recordsLinked to original sources

Bidirectional Crosstalk Between the SAGA Complex Deubiquitinase Module and the Molecular Circadian Clock

The Spt-Ada-Gcn5-acetyltransferase (SAGA) complex is a highly conserved chromatin-modifying transcriptional coactivator that regulates gene expression through both transcriptional and post-translational mechanisms. In addition to histone acetyltransferase activity, SAGA harbors a deubiquitinase module (DUBm) that influences protein stability, localization, and function by removal of ubiquitin. Although SAGAs roles in transcription are well characterized, how its enzymatic modules are dynamically regulated to coordinate its divergent activities remains less known. Here, we identify a bidirectional relationship between the molecular circadian clock and the SAGA DUBm. Our results indicate that circadian rhythms influence DUBm activities and expression, while the DUBm in turn shapes the timing and stability of core clock proteins and transcripts, positioning the DUBm as an important mediator of the molecular circadian clock.

neuroscience↗

The Arabidopsis TIRome informs the design of artificial TIR (Toll/interleukin-1 receptor) domain proteins

The TIR (Toll/interleukin-1 receptor) domain is an ancient protein module that functions in immune and cell death responses across the Tree of Life. TIR domains encoded by plants and prokaryotes function as enzymes to produce diverse small molecule immune signals. Plant genomes can encode hundreds of TIR-domain containing proteins - many of which confer important agricultural disease resistance as TIR-NLR (nucleotide-binding, leucine-rich repeat) immune receptors. Despite their importance, how natural variation influences TIR enzymatic output and immunity-associated cell death is largely unexplored. We assayed a complete collection of the TIR domains of Arabidopsis thaliana Col-0 (the "AtTIRome") to explore variation in TIR metabolite production and cell death signaling. Roughly half of the AtTIRome triggered cell death in transient assays. Artificial TIR proteins designed based on consensus sequences of the AtTIRomes cell death phenotypic classes revealed polymorphisms controlling variation in TIR cell death elicitation and metabolite production. Structure-function analyses of artificial TIRs revealed that natural variation in the "BB-loop", a flexible region overlying the catalytic pocket, determines differences in function across Arabidopsis TIR-containing proteins. We further demonstrate that artificial TIRs are functional on an NLR chassis and that BB-loop variation can tune the activity of a natural TIR-NLR protein. These findings shed light on the diversity of TIR outputs and reveal methods to design and engineer TIR-based immune receptors. Significance StatementTIR (Toll/interleukin-1 receptors) domain proteins perform immune signaling across the Tree of Life. TIR domains are enzymes that can process NAD+ to generate diverse small molecule signals. In order to better understand TIR-based signaling, we leveraged Arabidopsis natural variation across [~]150 TIR proteins to inform the design of artificial TIRs, define features that control output, and tune the output of a natural TIR immune receptor. The engineering of plant immune pathways will enable the optimization of disease resistance to safeguard yields.

plant biology↗

Genomic Analysis of Human Noroviruses Using Hybrid Illumina-Nanopore Data

Whole genome sequence (WGS) analysis of noroviruses is routinely performed by employing a metagenomic approach. While this methodology has several advantages, such as allowing for examination of co-infection, it has some limitations such as the requirement of high viral load to achieve full-length or near full-length genomic sequences. In this study, we used an amplification approach to obtain full-length genomic amplicons from 39 Canadian GII isolates followed by deep sequencing on Illumina and Oxford Nanopore platforms. This approach significantly reduced the required viral titre to obtain full-genome coverage. Herein, we compared the coverage and sequences obtained by both platforms and provided an in-depth genomic analysis of the obtained sequences, including the presence of single nucleotide variants (SNVs) and recombination events.

microbiology↗