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Francese, C.

Publications and source records attributed to Francese, C..

2 recordsLinked to original sources

An AI-driven pipeline for the discovery of hidden peptides in plant proteomes: the CLE family as a case study

Plant proteomes contain evolutionarily conserved peptides with poorly conserved primary sequences, often hindering their identification and classification into families. Homology-based approaches and conventional annotation pipelines frequently fail to detect these family members, particularly in poorly characterized, but agronomically relevant plant species. CLE peptides (CLAVATA3/EMBRYO SURROUNDING REGION-related peptides) constitute a large and evolutionarily conserved family of plant signaling molecules, yet their characterization remains incomplete. Beyond a limited number of well-studied members, a substantial number of CLE peptides remain uncharacterized due to functional redundancy and the intrinsic features of CLE genes, which encode short pre-propeptides with only a small 12-residue conserved motif. Here, we present a novel framework leveraging state-of-the-art Protein Language Models (pLMs) to discover CLE peptides directly from 13 plant proteomes. By coupling sequence embeddings trained on large evolutionary datasets (ESM2 and ProtT5) with supervised machine learning, our dual-model approach captures deep semantic features of the CLE family that are missed by traditional alignment methods. The pipeline demonstrated robust generalization, achieving high classification accuracy (98.9-99.4%) on a held-out set of CLE peptides not used during training. Consequently, we identified a set of high-confidence, previously unannotated CLE candidates prioritized through a stringent consensus-based filtering strategy. This work demonstrates how AI-driven proteome analysis can overcome the limitations of homology-based methods and provides a scalable strategy for uncovering previously unidentified peptide-mediated signaling molecules across plant lineages. HighlightLeveraging Protein Language Models, our AI framework uncovers "hidden" signaling peptides missed by standard tools, revealing the elusive diversity of CLE regulators across plant proteomes.

plant biology↗

Flavodiiron protein activity outcompetes cyclic electron transport when expressed in angiosperm Nicotiana tabacum

In conditions of excess illumination, alternative electron transport pathways in the thylakoid membranes protect the photosynthetic apparatus against damage from eventual over-reduction. Two main pathways downstream of photosystem I (PSI) enable alternative electron flow, mitigating PSI acceptor-side limitation, while contributing to ATP biosynthesis without reducing NADP+ to NADPH: cyclic electron transport (CET) and pseudo-cyclic electron transport (PCET). Flavodiiron proteins (FLV) are crucial enzymes in PCET, found in all photosynthetic organisms but lost during the evolution of angiosperms. The absence of FLV coding sequences in angiosperm genomes raises intriguing questions about their role and function in photosynthetic organisms. Previous studies utilizing heterologous expression have already demonstrated that FLV can function in angiosperms. In this study, Physcomitrium patens FLVA and FLVB coding sequences were stably expressed in wild-type Nicotiana tabacum, a model crop species. Transgenic lines exhibited significantly increased PCET rates, with FLV-dependent electron transport competing for electrons with CET, particularly under sudden increases in light intensity that limited acceptor side limitation. These findings indicate that FLVs are not only active but also play a critical role in protecting from over-reduction the photosynthetic apparatus of Nicotiana tabacum under fluctuating light conditions.

plant biology↗