bioRxivPlant BiologyPreprint
The prion-like domain of the chloroplast RNA binding protein CP29A is required for cold-induced phase separation next to nucleoids and supports RNA splicing and translation during cold acclimation
J. Legen, B. Lenzen, N. Kachariya, S. Feltgen, Y. Gao, S. Mergenthal, W. Weber, E. Klotzsch, R. Zoschke, M. Sattler, C. Schmitz-Linneweber
Abstract
Arabidopsis thaliana is capable of producing photosynthetic tissue with active chloroplasts at temperatures as low as 4{degrees}C, and this process depends on the presence of the nuclear-encoded, chloroplast-localized RNA-binding protein CP29A. In this study, we demonstrate that CP29A undergoes phase separation in vitro and in vivo in a temperature-dependent manner, which is mediated by a prion-like domain (PLD) located between the two RNA recognition motif (RRM) domains of CP29A. The resulting droplets display liquid-like properties and are found in close proximity to chloroplast nucleoids. The PLD is required to support chloroplast RNA splicing and translation in cold-treated tissue. Together, our findings suggest that plant chloroplast gene expression is compartmentalized by inducible condensation of CP29A at low temperatures, a mechanism that could play a crucial role for plant cold resistance.
- organism: Arabidopsis
- assay: proteomics
- research focus: cell type annotation
- research focus: gene regulatory network inference
- research focus: protein folding & dynamics
- approach: experimental assay
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