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Kuhlmann, A. B.

Publications and source records attributed to Kuhlmann, A. B..

2 recordsLinked to original sources

Epigenetic regulation of a heat-trainable sHSP locus controls thermomemory in a unicellular alga

A powerful way to enhance heat tolerance is to prime organisms with a moderate heat treatment to establish a molecular stress memory permitting the survival of the organism when exposed to subsequent heat shocks. While this has been extensively studied in multicellular organisms, we demonstrate that the unicellular red alga Cyanidioschyzon merolae exhibits heat stress memory. We show that, similarly to more complex organisms, thermomemory in this alga is underpinned by transcriptomic reprogramming, with the chloroplast emerging as the main site of gene trainability. Additionally, we find a conserved small heat shock protein (sHSP)-encoding locus in the nuclear genome to be heat-trainable, likely by histone depletion and sustained removal of the repressive mark histone H3 Lysine 27 trimethylation (H3K27me3). Of C. merolaes two sHSPs, only the nuclear-localizing CmsHSP2 is necessary for proper HS memory establishment. Finally, we reveal a role for the H3K27me3-transferase CmE(z) (Enhancer of zeste) in heat stress memory which shapes the transcriptome to recurring heat exposures, beyond regulating the trainable sHSP locus. Overall, our work provides a molecular framework for the regulation of heat stress memory in a unicellular eukaryote.

genetics↗

Cold stress induces a rapid redistribution of the antagonistic marks H3K4me3 and H3K27me3 in Arabidopsis thaliana

When exposed to low temperatures, plants undergo a drastic reprogramming of their transcriptome in order to adapt to their new environmental conditions, which primes them for potential freezing temperatures. While the involvement of transcription factors in this process, termed cold acclimation, has been deeply investigated, the potential contribution of chromatin regulation remains largely unclear. A large proportion of cold-inducible genes carries the repressive mark histone 3 lysine 27 trimethylation (H3K27me3), which has been hypothesized as maintaining them in a silenced state in the absence of stress, but which would need to be removed or counteracted upon stress perception. However, the fate of H3K27me3 during cold exposure has not been studied genome-wide. In this study, we offer an epigenome profiling of H3K27me3 and its antagonistic active mark H3K4me3 during short-term cold exposure. Both chromatin marks undergo rapid redistribution upon cold exposure, however, the gene sets undergoing H3K4me3 or H3K27me3 differential methylation are distinct, refuting the simplistic idea that gene activation relies on a switch from an H3K27me3 repressed chromatin to an active form enriched in H3K4me3. Coupling the ChIP-seq experiments with transcriptome profiling reveals that differential histone methylation correlates with changes in expression. Interestingly, only a subset of cold-regulated genes lose H3K27me3 during their induction, indicating that H3K27me3 is not an obstacle to transcriptional activation. In the H3K27me3 methyltransferase curly leaf (clf) mutant, many cold regulated genes display reduced H3K27me3 levels but their transcriptional activity is not altered prior or during a cold exposure, suggesting that H3K27me3 may serve a more intricate role in the cold response than simply repressing the cold-inducible genes in naive conditions.

plant biology↗