TY - JOUR
T1 - The mRNA covalent modification dihydrouridine regulates transcript turnover and photosynthetic capacity during plant abiotic stress
AU - Yu, Li’ang
AU - Melandri, Giovanni
AU - Dittrich, Anna C.Nelson
AU - Calleja, Sebastian
AU - Ganguly, Diep R.
AU - Palos, Kyle
AU - Brewer, Emily K.
AU - Fischer, Hillary
AU - Rozzi, Bruno
AU - Srinivasan, Aparna
AU - Obata, Toshihiro
AU - AbdElgawad, Hamada
AU - Beemster, Gerrit T.S.
AU - Henderson, Riley
AU - Garcia, Ciara
AU - Zhang, Xiaodan
AU - Stern, David
AU - Eveland, Andrea
AU - Lyons, Eric
AU - Arnold, A. Elizabeth
AU - Skirycz, Aleksandra
AU - Schroeder, Susan J.
AU - Gregory, Brian D.
AU - Pauli, Duke
AU - Nelson, Andrew D.L.
N1 -
© The Author(s) 2026.
PY - 2026/6/25
Y1 - 2026/6/25
N2 - RNA covalent modifications (RCMs) influence RNA stability and translation efficiency, and they thus play critical roles in eukaryotic growth and development. However, their role in regulating plant performance under abiotic stress remains largely unexplored. Here, we integrated multi-omics data in 6 Sorghum bicolor accessions under water-limiting conditions in the field to explore the relationship between RCMs and drought response. Within a stress- and photosynthesis-associated gene co-expression module, we identified SbDUS2, a member of a family of enzymes conserved across eukaryotes, that catalyzes the reduction of uracil to dihydrouridine (DHU) on RNA molecules. DHU-modified transcripts in this module were enriched for photosynthetic functions and showed strong correlation with photosynthetic traits. To elucidate the function of this RCM, we characterized loss-of-function dus2 mutants in Arabidopsis thaliana. Under control conditions, these DHU-deficient mutants exhibited impaired germination and delayed development. Furthermore, under water-limiting or heat conditions, these mutants showed significantly reduced net CO2 assimilation and survival. Using multiple transcriptome-wide RNA stability assays, we demonstrated that transcripts associated with lower DHU levels in a dus2 background generally exhibited increased stability compared to Col-0 controls. Particularly, lack of DUS2 led to the hyperstability of photosynthesis-related transcripts, impeding their turnover and likely preventing proper photosynthetic acclimation during stress. We propose a model where DHU acts as a critical post-transcriptional regulator marking mRNAs for rapid turnover under stress, highlighting an overlooked regulatory layer contributing to plant resilience.
AB - RNA covalent modifications (RCMs) influence RNA stability and translation efficiency, and they thus play critical roles in eukaryotic growth and development. However, their role in regulating plant performance under abiotic stress remains largely unexplored. Here, we integrated multi-omics data in 6 Sorghum bicolor accessions under water-limiting conditions in the field to explore the relationship between RCMs and drought response. Within a stress- and photosynthesis-associated gene co-expression module, we identified SbDUS2, a member of a family of enzymes conserved across eukaryotes, that catalyzes the reduction of uracil to dihydrouridine (DHU) on RNA molecules. DHU-modified transcripts in this module were enriched for photosynthetic functions and showed strong correlation with photosynthetic traits. To elucidate the function of this RCM, we characterized loss-of-function dus2 mutants in Arabidopsis thaliana. Under control conditions, these DHU-deficient mutants exhibited impaired germination and delayed development. Furthermore, under water-limiting or heat conditions, these mutants showed significantly reduced net CO2 assimilation and survival. Using multiple transcriptome-wide RNA stability assays, we demonstrated that transcripts associated with lower DHU levels in a dus2 background generally exhibited increased stability compared to Col-0 controls. Particularly, lack of DUS2 led to the hyperstability of photosynthesis-related transcripts, impeding their turnover and likely preventing proper photosynthetic acclimation during stress. We propose a model where DHU acts as a critical post-transcriptional regulator marking mRNAs for rapid turnover under stress, highlighting an overlooked regulatory layer contributing to plant resilience.
UR - https://www.scopus.com/pages/publications/105045818391
U2 - 10.1093/plcell/koag196
DO - 10.1093/plcell/koag196
M3 - Article
AN - SCOPUS:105045818391
SN - 1040-4651
VL - 38
JO - Plant Cell
JF - Plant Cell
IS - 7
M1 - koag196
ER -