Evidence map›Paper›PMID 40830753›Full record

ArticleBMC bioinformatics2025

NetStart 2.0: prediction of eukaryotic translation initiation sites using a protein language model.

Line Sandvad Nielsen, Anders Gorm Pedersen, Ole Winther, Henrik Nielsen

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Frameshift Mutations in Exon 1 ofJournal of developmental biology · 2026
    Article
  3. Article
  4. Article
  5. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Line Sandvad NielsenSection for Computational and RNA Biology, Department of Biology, University of Copenhagen, 2200, Copenhagen, Denmark. line.s.nielsen@bio.ku.dk.
Anders Gorm PedersenSection for Bioinformatics, Department of Health Technology, Technical University of Denmark, 2800, Kongens Lyngby, Denmark.
Ole WintherSection for Computational and RNA Biology, Department of Biology, University of Copenhagen, 2200, Copenhagen, Denmark.
Henrik NielsenSection for Bioinformatics, Department of Health Technology, Technical University of Denmark, 2800, Kongens Lyngby, Denmark. henni@dtu.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate identification of translation initiation sites is essential for the proper translation of mRNA into functional proteins. In eukaryotes, the choice of the translation initiation site is influenced by multiple factors, including its proximity to the 5[Formula: see text] end and the local start codon context. Translation initiation sites mark the transition from non-coding to coding regions. This fact motivates the expectation that the upstream sequence, if translated, would assemble a nonsensical order of amino acids, while the downstream sequence would correspond to the structured beginning of a protein. This distinction suggests potential for predicting translation initiation sites using a protein language model.

resultsWe present NetStart 2.0, a deep learning-based model that integrates the ESM-2 protein language model with the local sequence context to predict translation initiation sites across a broad range of eukaryotic species. NetStart 2.0 was trained as a single model across multiple species, and despite the broad phylogenetic diversity represented in the training data, it consistently relied on features marking the transition from non-coding to coding regions.

conclusionBy leveraging "protein-ness", NetStart 2.0 achieves state-of-the-art performance in predicting translation initiation sites across a diverse range of eukaryotic species. This success underscores the potential of protein language models to bridge transcript- and peptide-level information in complex biological prediction tasks. The NetStart 2.0 webserver is available at: https://services.healthtech.dtu.dk/services/NetStart-2.0/ .

Indexed as

Computational BiologyEukaryotaPeptide Chain Initiation, TranslationalSoftwareCodon, InitiatorDeep LearningHumansRNA, MessengerCodon, InitiatorRNA, MessengerCoding potentialDeep learningEukaryotic translation initiationProtein language models“Protein-ness”Start codonsTranslation initiation sites

Identifiers

PMID40830753
PMCPMC12366053

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.