학술논문

Evolutionarily recent retrotransposons contribute to schizophrenia.
Document Type
article
Source
Translational psychiatry. 13(1)
Subject
Brain
Humans
Retroelements
Schizophrenia
Haplotypes
Quantitative Trait Loci
Human Genome
Serious Mental Illness
Genetics
Neurosciences
Brain Disorders
Mental Health
Aetiology
Underpinning research
2.1 Biological and endogenous factors
1.1 Normal biological development and functioning
Mental health
Clinical Sciences
Public Health and Health Services
Psychology
Language
Abstract
Transposable elements (TEs) are mobile genetic elements that constitute half of the human genome. Recent studies suggest that polymorphic non-reference TEs (nrTEs) may contribute to cognitive diseases, such as schizophrenia, through a cis-regulatory effect. The aim of this work is to identify sets of nrTEs putatively linked to an increased risk of developing schizophrenia. To do so, we inspected the nrTE content of genomes from the dorsolateral prefrontal cortex of schizophrenic and control individuals and identified 38 nrTEs that possibly contribute to the emergence of this psychiatric disorder, two of them further confirmed with haplotype-based methods. We then performed in silico functional inferences and found that 9 of the 38 nrTEs act as expression/alternative splicing quantitative trait loci (eQTLs/sQTLs) in the brain, suggesting a possible role in shaping the human cognitive genome structure. To our knowledge, this is the first attempt at identifying polymorphic nrTEs that can contribute to the functionality of the brain. Finally, we suggest that a neurodevelopmental genetic mechanism, which involves evolutionarily young nrTEs, can be key to understanding the ethio-pathogenesis of this complex disorder.