Skip to content
Open access

Unlocking cis-regulatory landscapes across 500 million years of evolution and disease mechanisms

Jun 2026 · NAR Genomics and Bioinformatics · Vol 8 · 0 citations · 156 references
Medicine

TL;DR

The Vertebrate Regulatory MOdule Detector (VRMOD) provides a universal coordinate reference system for regulatory sequences across 309 vertebrate genomes and enables genome-wide annotation of non-coding regulatory elements in any vertebrate species using genomic sequence alone.

Abstract

Abstract Genomic DNA encodes regulatory information that determines where, when, and to what extent genes are expressed. Theoretically, we should be able to identify these transcriptional “instructions” by examining genomic DNA sequence alone, yet this has remained challenging. Here we present the Vertebrate Regulatory MOdule Detector (VRMOD), a method that accurately predicts gene regulatory sequences using only the query genomic sequences. We applied VRMOD to 309 Ensembl genomes, generating a compendium of high-resolution, genome-position-fixed cis-regulatory modules without parameter tuning. We performed extensive computational evaluation and experimental validation of VRMOD predictions. Notably, VRMOD predicted three sub-enhancers within the human hs52 enhancer at the FTO locus from the VISTA database, including one missed by existing methods. Using a chicken embryo system and 3D tissue imaging, we showed that each sub-enhancer exhibits restricted spatiotemporal activity within specific subsets of tissues where the full enhancer is active. We further demonstrated VRMOD’s utility for identifying evolutionarily non-conserved enhancers, annotating regulatory sequences in non-model organisms, and identifying candidate disease-causal variants. Collectively, VRMOD provides a universal coordinate reference system for regulatory sequences across 309 vertebrate genomes and enables genome-wide annotation of non-coding regulatory elements in any vertebrate species using genomic sequence alone.

Read PDF

Similar papers

Review Open access Sep 2026

From reference-genome prediction to causal generalization: sequence-to-function models for plant regulatory genomics

This Mini Review summarizes seq2func modelling in plant regulatory genomics, discusses plant-specific challenges and the complementary value of observational and perturbation assays, and proposes evaluation frameworks based on biologically meaningful distribution shifts.

Ming-Fang Zhan, Rui-Gang Wu · 0 citations
Review Open access Aug 2026

Active Human Transposable Elements: Long-Read Sequencing Technologies, Computational Analysis, and Implications for Human Disease

The biology of active human TE is summarized, state-of-the-art short- and long-read pipelines for TE analysis are surveyed, and their applications in studies of aging, cancer, and other complex diseases are highlighted.

Dániel Vörösvácki, Nikolett Szakállas, Alexandra Kalmár et al. · 0 citations
Open access Oct 2026

Landscape and mutational dynamics of G-quadruplexes across the complete human genome

G-quadruplexes (G4s) are alternative DNA structures with diverse biological roles, but their examination in highly repetitive parts of the human genome has been hindered by the lack of reliable sequencing technologies. Recent long-read based genome assemblies have enabled their characterization in previously inac...

Nikol Chantzi, Shi Wei. Liew, Aurell Wijaya et al. · 0 citations
Review Open access Aug 2026

Deep Learning for Deciphering the Plant Cis-Regulatory Code

This review compares convolutional, Transformer-based and graph architectures used to represent local sequence features, chromatin state and three-dimensional genome organisation to their applications to transcription-factor binding, chromatin accessibility, gene expression, non-coding variant prioritisation and regula...

Zhi-Meng Zhao, Si-Xuan Huang, Shi-Long Zhang et al. · 0 citations
Open access Aug 2026

Sequence-to-function deep learning decodes human cis-regulatory evolution

Deciphering the regulatory consequences of sequence divergence across human evolution is essential to understanding the molecular basis of human-specific traits and disease. Although millions of derived alleles distinguish humans from great apes, only a small fraction are likely to influence human-specific traits. Prev...

Riley J. Mangan, Nikitha Thoduguli, Dimitar Ivanov et al. · 0 citations
Open access Sep 2026

Genomic language model for predicting enhancers and their allele-specific activity in the human genome

It is shown that genome-wide enhancer annotations and candidate genetic variants predicted by DNABERT-Enhancer provide valuable resources for genome interpretation in functional and clinical genomics studies and can be explored interactively via the web application.

Rekha Sathian, P. Dutta, Ferhat Ay et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.