MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size

Author:

Lafferty Michael J12ORCID,Aygün Nil12,Patel Niyanta K12,Krupa Oleh12,Liang Dan12,Wolter Justin M1234,Geschwind Daniel H5678ORCID,de la Torre-Ubieta Luis8,Stein Jason L124ORCID

Affiliation:

1. Department of Genetics, University of North Carolina at Chapel Hill

2. UNC Neuroscience Center, University of North Carolina at Chapel Hill

3. Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill

4. Carolina Institute for Developmental Disabilities, The University of North Carolina at Chapel Hill

5. Neurogenetics Program, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles

6. Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, University of California, Los Angeles

7. Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles

8. Department of Psychiatry and Biobehavioral Sciences, Semel Institute, David Geffen School of Medicine, University of California, Los Angeles

Abstract

Expression quantitative trait loci (eQTL) data have proven important for linking non-coding loci to protein-coding genes. But eQTL studies rarely measure microRNAs (miRNAs), small non-coding RNAs known to play a role in human brain development and neurogenesis. Here, we performed small-RNA sequencing across 212 mid-gestation human neocortical tissue samples, measured 907 expressed miRNAs, discovering 111 of which were novel, and identified 85 local-miRNA-eQTLs. Colocalization of miRNA-eQTLs with GWAS summary statistics yielded one robust colocalization of miR-4707–3p expression with educational attainment and brain size phenotypes, where the miRNA expression increasing allele was associated with decreased brain size. Exogenous expression of miR-4707–3p in primary human neural progenitor cells decreased expression of predicted targets and increased cell proliferation, indicating miR-4707–3p modulates progenitor gene regulation and cell fate decisions. Integrating miRNA-eQTLs with existing GWAS yielded evidence of a miRNA that may influence human brain size and function via modulation of neocortical brain development.

Funder

National Institutes of Health

National Institute of General Medical Sciences

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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