Mutation of the polyadenylation complex subunit CstF77 reveals that mRNA 3′ end formation and HSP101 levels are critical for a robust heat stress response

Heat shock protein 101 (HSP101) in plants, and bacterial and yeast orthologs, is essential for thermotolerance. To investigate thermotolerance mechanisms involving HSP101, we performed a suppressor screen in Arabidopsis thaliana of a missense HSP101 allele (hot1-4). hot1-4 plants are sensitive to acclimation heat treatments that are otherwise permissive for HSP101 null mutants, indicating that the hot1-4 protein is toxic. We report one suppressor (shot2, suppressor of hot1-4 2) has a missense mutation of a conserved residue in CLEAVAGE STIMULATION FACTOR77 (CstF77), a subunit of the polyadenylation complex critical for mRNA 3 ' end maturation. We performed ribosomal RNA depletion RNA-Seq and captured transcriptional readthrough with a custom bioinformatics pipeline. Acclimation heat treatment caused transcriptional readthrough in hot1-4 shot2, with more readthrough in heat-induced genes, reducing the levels of toxic hot1-4 protein and suppressing hot1-4 heat sensitivity. Although shot2 mutants develop like the wild type in the absence of stress and survive mild heat stress, reduction of heat-induced genes and decreased HSP accumulation makes shot2 in HSP101 null and wild-type backgrounds sensitive to severe heat stress. Our study reveals the critical function of CstF77 for 3 ' end formation of mRNA and the dominant role of HSP101 in dictating the outcome of severe heat stress.

Automated summary

Studies revealed that heat shock protein 101 (HSP101) is essential for thermotolerance in plants, bacteria, and yeast. Through a suppressor screen in Arabidopsis thaliana, a mutation in the CLEAVAGE STIMULATION FACTOR77 (CstF77) gene was identified as a suppressor of hot1-4, suggesting its critical role in mRNA 3' end maturation. The dominant role of HSP101 in severe heat stress outcome was also demonstrated.