학술논문

Conserved and divergent gene regulatory programs of the mammalian neocortex.
Document Type
article
Source
Nature. 624(7991)
Subject
Animals
Humans
Mice
Callithrix
Chromatin
Conserved Sequence
DNA Methylation
DNA Transposable Elements
Epigenome
Evolution
Molecular
Gene Expression Regulation
Gene Regulatory Networks
Macaca
Mammals
Motor Cortex
Multiomics
Neocortex
Regulatory Sequences
Nucleic Acid
Single-Cell Analysis
Transcription Factors
Genetic Variation
Language
Abstract
Divergence of cis-regulatory elements drives species-specific traits1, but how this manifests in the evolution of the neocortex at the molecular and cellular level remains unclear. Here we investigated the gene regulatory programs in the primary motor cortex of human, macaque, marmoset and mouse using single-cell multiomics assays, generating gene expression, chromatin accessibility, DNA methylome and chromosomal conformation profiles from a total of over 200,000 cells. From these data, we show evidence that divergence of transcription factor expression corresponds to species-specific epigenome landscapes. We find that conserved and divergent gene regulatory features are reflected in the evolution of the three-dimensional genome. Transposable elements contribute to nearly 80% of the human-specific candidate cis-regulatory elements in cortical cells. Through machine learning, we develop sequence-based predictors of candidate cis-regulatory elements in different species and demonstrate that the genomic regulatory syntax is highly preserved from rodents to primates. Finally, we show that epigenetic conservation combined with sequence similarity helps to uncover functional cis-regulatory elements and enhances our ability to interpret genetic variants contributing to neurological disease and traits.