Nucleotide dependency analysis of DNA language models reveals genomic functional elements

• Published in: bioRxiv
• Main Authors: Tomaz da Silva, Pedro, Karollus, Alexander, Hingerl, Johannes, Galindez, Gihanna, Wagner, Nils, Hernandez-Alias, Xavier, Incarnato, Danny, Gagneur, Julien
• Format: Paper
• Language: English
• Published: Cold Spring Harbor Laboratory 27.07.2024
• Edition: 1.1
• Subjects: Genomics
• DOI: 10.1101/2024.07.27.605418

Deciphering how nucleotides in genomes encode regulatory instructions and molecular machines is a long-standing goal in biology. DNA language models (LMs) implicitly capture functional elements and their organization from genomic sequences alone by modeling probabilities of each nucleotide given its sequence context. However, using DNA LMs for discovering functional genomic elements has been challenging due to the lack of interpretable methods. Here, we introduce nucleotide dependencies which quantify how nucleotide substitutions at one genomic position affect the probabilities of nucleotides at other positions. We generated genome-wide maps of pairwise nucleotide dependencies within kilobase ranges for animal, fungal, and bacterial species. We show that nucleotide dependencies indicate deleteriousness of human genetic variants more effectively than sequence alignment and DNA LM reconstruction. Regulatory elements appear as dense blocks in dependency maps, enabling the systematic identification of transcription factor binding sites as accurately as models trained on experimental binding data. Nucleotide dependencies also highlight bases in contact within RNA structures, including pseudoknots and tertiary structure contacts, with remarkable accuracy. This led to the discovery of four novel, experimentally validated RNA structures in Escherichia coli. Finally, using dependency maps, we reveal critical limitations of several DNA LM architectures and training sequence selection strategies by benchmarking and visual diagnosis. Altogether, nucleotide dependency analysis opens a new avenue for discovering and studying functional elements and their interactions in genomes.