Andres V. Reyes

The paper shows CDK8 phosphorylates DELLA to limit Mediator recruitment, affecting GA signaling in Arabidopsis.

The paper demonstrates that lamin-B3 can assemble into filamentous structures in Xenopus laevis egg extracts under nucleoplasm-like conditions, independent of nuclear assembly.

This study maps protein-protein interactions in Arabidopsis using cross-linking mass spectrometry, identifying thousands of interactions across subcellular compartments and structural complexes.

The paper identifies CKL3 and Nup58 as key regulators of effector-triggered immunity by linking Ca2+ influx to nuclear transport reprogramming.

This study provides large-scale proteomic evidence that alternative splicing isoforms are translated in plants, showing their impact on protein abundance and plant growth.

This study identifies BAM1D as a co-receptor interacting with FEA3 in maize, revealing antagonistic genetic interactions that regulate inflorescence meristem size.

The paper uses proteomic analysis to identify substrate proteins regulated by O-fucosylation and O-GlcNAcylation in Arabidopsis, revealing their roles in protein homeostasis and stress responses.

This study identifies BSL1 as a plant-specific phosphatase that dephosphorylates CDKB1 to promote mitotic entry by counteracting phosphorylation at T14/Y15 residues.

The paper identifies CSC and REM as mechanisms mediating plant cell resilience through cell wall-plasma membrane attachments under hyperosmotic stress.

The paper maps the Arabidopsis alternative splicing machinery and identifies O-glycosylation regulators affecting splicing through ACINUS-dependent and -independent pathways.

The paper identifies ZNF574 as a key factor in a quality control pathway that degrades defective ribosome intermediates in human cells.

The paper improves TurboID-mediated proximity labeling by optimizing enrichment and analysis methods, identifying 160 SPY interactors including 100 novel ones.

The paper identifies the interactome of TERT in Trypanosoma brucei using mass spectrometry, revealing unique telomerase interactions in this parasite.