» Articles » PMID: 37941140

Multiple Sequence Alignment-based RNA Language Model and Its Application to Structural Inference

Overview
Specialty Biochemistry
Date 2023 Nov 9
PMID 37941140
Authors
Affiliations
Soon will be listed here.
Abstract

Compared with proteins, DNA and RNA are more difficult languages to interpret because four-letter coded DNA/RNA sequences have less information content than 20-letter coded protein sequences. While BERT (Bidirectional Encoder Representations from Transformers)-like language models have been developed for RNA, they are ineffective at capturing the evolutionary information from homologous sequences because unlike proteins, RNA sequences are less conserved. Here, we have developed an unsupervised multiple sequence alignment-based RNA language model (RNA-MSM) by utilizing homologous sequences from an automatic pipeline, RNAcmap, as it can provide significantly more homologous sequences than manually annotated Rfam. We demonstrate that the resulting unsupervised, two-dimensional attention maps and one-dimensional embeddings from RNA-MSM contain structural information. In fact, they can be directly mapped with high accuracy to 2D base pairing probabilities and 1D solvent accessibilities, respectively. Further fine-tuning led to significantly improved performance on these two downstream tasks compared with existing state-of-the-art techniques including SPOT-RNA2 and RNAsnap2. By comparison, RNA-FM, a BERT-based RNA language model, performs worse than one-hot encoding with its embedding in base pair and solvent-accessible surface area prediction. We anticipate that the pre-trained RNA-MSM model can be fine-tuned on many other tasks related to RNA structure and function.

Citing Articles

Foundation models in bioinformatics.

Guo F, Guan R, Li Y, Liu Q, Wang X, Yang C Natl Sci Rev. 2025; 12(4):nwaf028.

PMID: 40078374 PMC: 11900445. DOI: 10.1093/nsr/nwaf028.


RNA sequence analysis landscape: A comprehensive review of task types, databases, datasets, word embedding methods, and language models.

Asim M, Ibrahim M, Asif T, Dengel A Heliyon. 2025; 11(2):e41488.

PMID: 39897847 PMC: 11783440. DOI: 10.1016/j.heliyon.2024.e41488.


RNAbpFlow: Base pair-augmented SE(3)-flow matching for conditional RNA 3D structure generation.

Tarafder S, Bhattacharya D bioRxiv. 2025; .

PMID: 39896539 PMC: 11785242. DOI: 10.1101/2025.01.24.634669.


Overview and Prospects of DNA Sequence Visualization.

Wu Y, Xie X, Zhu J, Guan L, Li M Int J Mol Sci. 2025; 26(2).

PMID: 39859192 PMC: 11764684. DOI: 10.3390/ijms26020477.


Robust RNA secondary structure prediction with a mixture of deep learning and physics-based experts.

Qiu X Biol Methods Protoc. 2025; 10(1):bpae097.

PMID: 39811444 PMC: 11729747. DOI: 10.1093/biomethods/bpae097.


References
1.
Fu L, Niu B, Zhu Z, Wu S, Li W . CD-HIT: accelerated for clustering the next-generation sequencing data. Bioinformatics. 2012; 28(23):3150-2. PMC: 3516142. DOI: 10.1093/bioinformatics/bts565. View

2.
Steinegger M, Meier M, Mirdita M, Vohringer H, Haunsberger S, Soding J . HH-suite3 for fast remote homology detection and deep protein annotation. BMC Bioinformatics. 2019; 20(1):473. PMC: 6744700. DOI: 10.1186/s12859-019-3019-7. View

3.
Kalvari I, Nawrocki E, Ontiveros-Palacios N, Argasinska J, Lamkiewicz K, Marz M . Rfam 14: expanded coverage of metagenomic, viral and microRNA families. Nucleic Acids Res. 2020; 49(D1):D192-D200. PMC: 7779021. DOI: 10.1093/nar/gkaa1047. View

4.
Alley E, Khimulya G, Biswas S, AlQuraishi M, Church G . Unified rational protein engineering with sequence-based deep representation learning. Nat Methods. 2019; 16(12):1315-1322. PMC: 7067682. DOI: 10.1038/s41592-019-0598-1. View

5.
Elnaggar A, Heinzinger M, Dallago C, Rehawi G, Wang Y, Jones L . ProtTrans: Toward Understanding the Language of Life Through Self-Supervised Learning. IEEE Trans Pattern Anal Mach Intell. 2021; 44(10):7112-7127. DOI: 10.1109/TPAMI.2021.3095381. View