학술논문

Reintroduction of the archaic variant of NOVA1 in cortical organoids alters neurodevelopment
Document Type
article
Source
Science. 371(6530)
Subject
Stem Cell Research - Induced Pluripotent Stem Cell
Neurosciences
Genetics
Human Genome
Stem Cell Research
Underpinning research
1.1 Normal biological development and functioning
Neurological
Alleles
Alternative Splicing
Amino Acid Substitution
Animals
Binding Sites
Biological Evolution
CRISPR-Cas Systems
Cell Proliferation
Cerebral Cortex
Gene Expression Regulation
Developmental
Genetic Variation
Genome
Genome
Human
Haplotypes
Hominidae
Humans
Induced Pluripotent Stem Cells
Neanderthals
Nerve Net
Nerve Tissue Proteins
Neuro-Oncological Ventral Antigen
Neurons
Organoids
RNA-Binding Proteins
Synapses
General Science & Technology
Language
Abstract
The evolutionarily conserved splicing regulator neuro-oncological ventral antigen 1 (NOVA1) plays a key role in neural development and function. NOVA1 also includes a protein-coding difference between the modern human genome and Neanderthal and Denisovan genomes. To investigate the functional importance of an amino acid change in humans, we reintroduced the archaic allele into human induced pluripotent cells using genome editing and then followed their neural development through cortical organoids. This modification promoted slower development and higher surface complexity in cortical organoids with the archaic version of NOVA1 Moreover, levels of synaptic markers and synaptic protein coassociations correlated with altered electrophysiological properties in organoids expressing the archaic variant. Our results suggest that the human-specific substitution in NOVA1, which is exclusive to modern humans since divergence from Neanderthals, may have had functional consequences for our species' evolution.