HydraRNA: a hybrid architecture based full-length RNA language model
Open accessPublished version of a preprint
Abstract
BACKGROUND: RNA, an essential component of the central dogma of molecular biology, plays versatile roles in all cellular processes. RNA large language models (LLMs) are emerging as powerful methods in RNA research to decipher its intricate network of function and regulation. However, previous RNA LLMs were based on the Transformer model and pre-trained on short segment of non-coding RNAs, which limits their general usability. Here we present the first full-length RNA foundation model, HydraRNA, which is based on a hybrid architecture of bidirectional state space model and multi-head attention mechanism. RESULTS: HydraRNA is pre-trained on a large amount of both protein-coding mRNAs and non-coding RNAs. Despite being pre-trained with the fewest parameters and the least GPU resources, HydraRNA learns better RNA representations and outperforms the existing foundation models on a variety of mRNA-related tasks, including coding/non-coding RNA classification, prediction of RNA secondary structure, RBP binding sites, splicing and polyadenylation sites, mRNA stability and translation efficiency. Furthermore, HydraRNA can accurately predict the effect of mutations and estimate the relative contributions of different mRNA regions to the RNA stability and translation. CONCLUSIONS: Our results demonstrate that the hybrid architecture outperforms the pure Transformer architectures in RNA language modeling. We anticipate that HydraRNA will enable dissecting the diverse properties of mRNA, accelerating the research of mRNA regulation and facilitating the optimal design of mRNA therapeutics.
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References 60 · Cited by 10
- Authors
- Li, G., Jiang, F., Zhu, J., Cui, H., Wang, Z., & Chen, W.
- Affiliations
- Southern University of Science and Technology (CN)
- Corresponding author
- Li, Guipeng
- Venue
- Genome Biology
- Published
- 2025-11-10
- Volume
- 26
- Issue
- 1
- Pages
- 383-383
- ISSN
- 1465-6906 (ISSN-L)
- 1474-760X
- PMC
- PMC12604409
- OpenAlex
- W4416088662
- Cited by
- 10
- References
- 60
- Citations by year
- 2026: 8 · 2025: 2
- FWCI
- 3.01
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Genome biology (publishedVersion, cc-by-nc-nd)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Zenodo (CERN European Organization for Nuclear Research)
- Funders
- National Key R&D Program of China (2022YFC3400400)
- Shenzhen Science and Technology Program (KQTD20180411143432337)
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology (ZDSYS20200811144002008)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Keywords
- RNA language models, bidirectional state space model, multi-head attention, hybrid architecture, mRNA stability, translation efficiency, mutation effect prediction, mRNA regulation
- MeSH terms
- Large Language Models, Nucleic Acid Conformation, RNA, RNA, Messenger, RNA, Untranslated
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