Post-translational modifications (PTMs) play crucial regulatory roles in plants, orchestrating protein functions to maintain metabolic homeostasis, enable adaptation to dynamic environments, and regulate diverse cellular processes. Thus, the identification of PTM sites is essential for elucidating the mechanisms underlying plant growth, development, and stress responses. However, reliable and cost-effective computational approaches for predicting PTM sites in plants remain lacking. Here, we present PlantPTM, an integrated deep learning framework for predicting nine PTM types in plants. By combining protein language models (PLMs) with evolutionary information, PlantPTM demonstrates robust generalizability across a wide range of PTM types and plant species. Our method achieves state-of-the-art performance, with a mean AUROC of 0.8640 and a peak AUROC of 0.9699 across the nine PTM types. Notably, PlantPTM maintains strong performance even under low-data scenarios and unseen species. Extensive comparative benchmarks demonstrate that PlantPTM outperforms existing PTM prediction tools by an average of 15.46%, with improvements ranging from 2.90% to 19.08% over the best-performing tools for each PTM type. Furthermore, independent in-house MS data confirmed the accuracy of PlantPTM for ubiquitination, acetylation, and N-glycosylation sites, with all AUROC values exceeding 0.8. To facilitate PTM studies in plants, we provide the PlantPTM online service and source code freely available at https://ai4bio.online/PlantPTM and https://github.com/wky0422/PlantPTM, respectively.
Homologous replacement of genomic sequences with large DNA fragments (> 100 bp) holds great potential for crop breeding, yet an efficient method to achieve such edits is lacking in plants. Here, in rice, we developed template-jumping prime editing (TJ-PE), a recently reported PE strategy for large targeted insertion, as an efficient tool for homologous replacement with DNA fragments ranging from dozens to hundreds of base pairs, and using TJ-PE, we replaced genomic fragments of up to 340 bp with homologous fragments of the same length. In addition, our TJ-PE tool also enabled precise deletion of 944- to 2024-bp fragments in rice, with efficiencies of up to 34.6% for c. 2000-bp precise deletions. Collectively, this study expands the editing scope of PE in rice and establishes TJ-PE as a generalist tool for precise deletion and replacement of large DNA fragments.
Huixia Liu, Yu Wang, Shuhui Guan et al.· New Phytologist· 0 citations