Year: 2026
Type: preprint
Abstract: The Arabidopsis transcriptome must be continuously reshaped to integrate endogenous and environmental cues, including the circadian clock and ambient light. This reprogramming relies on the coordinated synthesis and degradation of mRNAs, yet the contribution of RNA decay factors to circadian regulation remains poorly characterized. Here, we show that nearly all core clock genes are high-amplitude clock-controlled genes (HA-CCGs). A meta-analysis of transcriptome-wide mRNA decay datasets revealed that HA-CCGs have consistently shorter half-lives across multiple studies. We further identify the mRNA decapping activator DECAPPING PROTEIN 5 (DCP5) as a key regulator of circadian RNA stability. Using iCLIP, we show that DCP5 binds preferentially to HA-CCG transcripts at AU-rich motifs in their 3′ UTRs, thereby modulating their stability. Accordingly, the dcp5 mutant displays an extended circadian period at both physiological and molecular levels. Our findings establish mRNA decay as a post-transcriptional regulatory layer that fine-tunes the decay of multiple key transcripts within the circadian system.
Authors: Daniel Alejandro Careno, Soledad Perez Santangelo, Julieta Lisa Lisa Mateos, Luciana Bianchimano, Horacio Pallares, Dominique Jacques-Vuarambon, Micaela Sol Shalom, Abril San Martin, Maria Jose de Leone, Victor Daniel Aldas Bulos, Anthony Treichel, Martin Lewinski, Rodrigo Siqueira Reis, Dorothee Staiger, Ariel Alejandro Bazzini, Marcelo Javier Yanovsky
Language: English
Subfield: Plant Science
Domain: Life Sciences
Open Access status: green
Awards: G1634520576, G2779811793, G690099935
OpenAlex ID: W7225123990
