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The Function of LncRNA DRIR in Freezing Tolerance by Promoting Autophagic Degradation of CP29A and CP29B to Alter Alternative Splicing Patterns of Pre-mRNAs

Preprint Created on 27 May 2026 bioRxiv

Research on the functions and molecular mechanisms of long non-coding RNAs (lncRNAs) involved in regulating plant freezing tolerance is still in its infancy. Our previous work identified that the lncRNA DROUGHT INDUCED LNCRNA (DRIR) regulates gene expression in Arabidopsis; however, the underlying molecular mechanism remains unknown. This study demonstrates that lncRNA DRIR regulates plant freezing tolerance by affecting the alternative splicing patterns of pre-mRNAs. Through chromatin isolation by RNA purification followed by mass spectrometry (ChIRP-MS), we identified two DRIR-interacting proteins: CP29A and CP29B. We showed that the drirD mutant, which exhibits elevated DRIR expression, and DRIR overexpression lines displayed increased sensitivity to freezing stress, whereas DRIR RNAi lines were more tolerant to the stress. CP29A and CP29B bind to nuclear transcripts and, together with DRIR, regulate pre-mRNA alternative splicing under freezing stress. Notably, DRIR induces the relocalization of CP29A and CP29B to autophagosomes, leading to autophagy-mediated protein degradation. Collectively, our findings elucidate the molecular mechanism by which DRIR influences the autophagy-based degradation of its binding proteins CP29A and CP29B, thereby regulating plant freezing tolerance by altering the alternative splicing patterns of pre-mRNAs. This provides novel insights into the functions and mechanisms of lncRNAs in plants adapting to freezing environments.

Ye, l., Tang, X., Yang, J., Qiang, Z., Wang, C., Xiong, L., Qin, T.

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