De novo network analysis reveals autism causal genes and developmental links to co-occurring traits.
Catriona J MillerEvgeniia GolovinaJoerg S WickerJessie C JacobsenJustin Martin O'SullivanPublished in: Life science alliance (2023)
Autism is a complex neurodevelopmental condition that manifests in various ways. Autism is often accompanied by other conditions, such as attention-deficit/hyperactivity disorder and schizophrenia, which can complicate diagnosis and management. Although research has investigated the role of specific genes in autism, their relationship with co-occurring traits is not fully understood. To address this, we conducted a two-sample Mendelian randomisation analysis and identified four genes located at the 17q21.31 locus that are putatively causal for autism in fetal cortical tissue ( LINC02210 , LRRC37A4P , RP11-259G18.1 , and RP11-798G7.6 ). LINC02210 was also identified as putatively causal for autism in adult cortical tissue. By integrating data from expression quantitative trait loci, genes and protein interactions, we identified that the 17q21.31 locus contributes to the intersection between autism and other neurological traits in fetal cortical tissue. We also identified a distinct cluster of co-occurring traits, including cognition and worry, linked to the genetic loci at 3p21.1. Our findings provide insights into the relationship between autism and co-occurring traits, which could be used to develop predictive models for more accurate diagnosis and better clinical management.
Keyphrases
- genome wide
- autism spectrum disorder
- intellectual disability
- attention deficit hyperactivity disorder
- dna methylation
- copy number
- long non coding rna
- network analysis
- poor prognosis
- high resolution
- bipolar disorder
- binding protein
- mild cognitive impairment
- bioinformatics analysis
- mass spectrometry
- transcription factor
- working memory
- young adults
- multiple sclerosis
- data analysis
- protein protein