Current limitations in predicting mRNA translation with deep learning models

The design of nucleotide sequences with defined properties is a long-standing problem in bioengineering. An important application is protein expression, be it in the context of research or the production of mRNA vaccines. The rate of protein synthesis depends on the 5' untranslated region (5�...

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Detalles Bibliográficos
Autores: Schlusser, Niels, Gonzalez Sevine, Asier|||0009-0009-0390-5482, Pandey, Muskan, Zavolan, Mihaela|||0000-0002-8832-2041
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:317831
Acceso en línea:https://ddd.uab.cat/record/317831
https://dx.doi.org/urn:doi:10.1186/s13059-024-03369-6
Access Level:acceso abierto
Palabra clave:Translation control
Deep learning
Explainable AI
Systems biology
Descripción
Sumario:The design of nucleotide sequences with defined properties is a long-standing problem in bioengineering. An important application is protein expression, be it in the context of research or the production of mRNA vaccines. The rate of protein synthesis depends on the 5' untranslated region (5'UTR) of the mRNAs, and recently, deep learning models were proposed to predict the translation output of mRNAs from the 5'UTR sequence. At the same time, large data sets of endogenous and reporter mRNA translation have become available. In this study, we use complementary data obtained in two different cell types to assess the accuracy and generality of currently available models for predicting translational output. We find that while performing well on the data sets on which they were trained, deep learning models do not generalize well to other data sets, in particular of endogenous mRNAs, which differ in many properties from reporter constructs. These differences limit the ability of deep learning models to uncover mechanisms of translation control and to predict the impact of genetic variation. We suggest directions that combine high-throughput measurements and machine learning to unravel mechanisms of translation control and improve construct design. The online version contains supplementary material available at 10.1186/s13059-024-03369-6.