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Biology subjects

Shur, G.

Publications and source records attributed to Shur, G..

3 recordsLinked to original sources

FAMUS: A Few-Shot Learning Framework for Large-Scale Protein Annotation

Predicting gene function is a pivotal and challenging step in genomic and metagenomic data analysis. Current automatic annotation tools typically rely on the single most similar sequence from the query database and struggle to robustly set hit thresholds for annotation. The sparsity of proteins per annotation makes it challenging to confidently assign gene function for underrepresented families. Here, we present a contrastive learning framework for functional annotation. FAMUS (Functional Annotation Method Using Supervised contrastive learning) compares query sequences to a full array of profile Hidden Markov Models and transforms the similarity scores into a condensed vector space that minimizes the distance of proteins from the same family. The similarity scores of a query to all profiles are used for its representation instead of considering only the top-ranking hit. Unannotated sequences are incorporated as negative examples during training, enabling robust detection of proteins that fall outside the scope of the reference database without requiring a user-defined threshold. Using this approach, FAMUS outperformed KEGGs native KofamScan for KEGG Orthology annotation and InterPros InterProScan for PANTHER family annotation. We thus created four protein annotation models using protein families from the KEGG Orthology, InterPro family, OrthoDB, and EggNOG databases. All four models are available as a conda package and via our user-friendly web server, allowing users to annotate large-scale datasets. FAMUS is the first comprehensive and modular annotation framework based on contrastive learning. It supports both pre-defined and user-specific databases for tailored annotation, and can be easily integrated into any genomic and metagenomic analysis pipeline to facilitate accurate, large-scale functional annotation.

bioinformatics↗

Phage-encoded homing endonucleases attenuate bacterial immunity

The arms race between bacteria and bacteriophages (phages) gave rise to multiple layers of antagonistic mechanisms, many of which remain unexplored. Here, we investigated the anti-phage defense system GAPS4 and showed that it is a non-selective DNase triggered by sensing DNA breaks. We further demonstrated that this activation mechanism renders GAPS4 a double-edged sword, sensitizing bacteria to various forms of antibacterial antagonism. Using comparative genomics, we found that phage-encoded homing endonucleases, long considered selfish mobile genetic elements, enhance phage fitness by attenuating GAPS4-mediated immunity. Our findings shed light on the evolutionary advantage provided by these ubiquitous mobile elements to their host phages, and on the intricate evolutionary cross-talk between bacteria and their predators.

microbiology↗

The predictive value of double-stranded RNA for A-to-I editing detection

Structured AbstractO_ST_ABSMotivationC_ST_ABSAdenosine-to-inosine (A-to-I) RNA editing, a crucial reaction for many processes that contribute to transcriptome plasticity, is both widely common across the transcriptome and difficult to predict due to a lack of distinctive genomic characteristics that can be obtained and analyzed computationally. An exception to this is the secondary structure of RNA molecules, which has been shown to have a major impact on the selectivity and specificity of the enzymes responsible for A-to-I editing. Yet, this information is rarely used for the task of editing site prediction. ResultsHere, we demonstrated the value of using base-pairing probabilities of RNA nucleotides to classify genomic sites as A-to-I RNA editing sites, using large-scale truth data which we compiled and make available for use in training future models. Our analysis suggests that the span of four bases from -2 (upstream) to +1 (downstream) of a putative editing site is most informative in this regard. A classifier trained on base-pairing probabilities alone performed with a positive predictive value (PPV) of 0.68, a negative predictive value (NPV) of 0.64, and an area under the receiver operating characteristic curve (AUC) of 0.71. By identifying structure-related features that are informative for detecting A-to-I RNA editing sites and quantifying their predictive value, this work advances our understanding of A-to-I editing determinants. AvailabilityAll source codes and data are available at https://github.com/Ally-s-Lab/P-BEP

bioinformatics↗