# SAE-RNA: A Sparse Autoencoder Model for Interpreting RNA Language Model Representations

arXiv: https://arxiv.org/abs/2510.02734 · HTML: https://mlsanity.com/paper/2510.02734/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Placed in Interpreting biomedical and science models, one of 13 directions in Mechanistic interpretability.
- Builds on 5 of its 15 references that are in the map.
- First posted on arXiv 3 Oct 2025.

## Placed in

- Mechanistic interpretability / [Interpreting biomedical and science models](https://mlsanity.com/mechinterp/interpreting-biomedical-and-science-models/)

## Builds on (most cited first, 5 of 5)

- [A Unified Approach to Interpreting Model Predictions](https://mlsanity.com/paper/1705.07874/) (2017)
- [Axiomatic Attribution for Deep Networks](https://mlsanity.com/paper/1703.01365/) (2017)
- [Sparse Autoencoders Find Highly Interpretable Features in Language Models](https://mlsanity.com/paper/2309.08600/) (2023)
- [InterPLM: Discovering Interpretable Features in Protein Language Models via Sparse Autoencoders](https://mlsanity.com/paper/2412.12101/) (2024)
- [RiNALMo: General-Purpose RNA Language Models Can Generalize Well on Structure Prediction Tasks](https://mlsanity.com/paper/2403.00043/) (2024)

## Abstract (arXiv)

Deep learning, particularly with the advancement of Large Language Models, has transformed biomolecular modeling, with protein language models such as ESM inspiring emerging RNA language models such as RiNALMo. Recent work has begun applying sparse autoencoders (SAEs) to protein language model representations, exploring representation-level interpretability in biomolecular models. Here, we explore whether SAEs can provide interpretable feature decompositions of RNA language model representations, while also examining their limitations in this setting. We present SAE-RNA, interpretability model that analyzes RiNALMo representations and maps them to known human-level biological features. Rather than claiming definitive biological concept discovery, our study frames SAE-based analysis as a representation-level probe for characterizing how RNA language models organize biological information internally. More broadly, SAE-RNA provides a feature-level framework for comparing RNA groups and identifying sparse representation components associated with RNA family identity or structural context.