General and specific patterns of cortical gene expression as spatial correlates of complex cognitive functioning

Author:

Moodie Joanna E.12ORCID,Harris Sarah E.1ORCID,Harris Mathew A.1,Buchanan Colin R.12ORCID,Davies Gail1ORCID,Taylor Adele1,Redmond Paul1,Liewald David C. M.1,Valdés Hernández Maria del C.123ORCID,Shenkin Susan134,Russ Tom C.135,Muñoz Maniega Susana123ORCID,Luciano Michelle1,Corley Janie1,Stolicyn Aleks3ORCID,Shen Xueyi3,Steele Douglas2ORCID,Waiter Gordon2,Sandu Anca‐Larisa2,Bastin Mark E.123,Wardlaw Joanna M.123ORCID,McIntosh Andrew3ORCID,Whalley Heather3ORCID,Tucker‐Drob Elliot M.6,Deary Ian J.1ORCID,Cox Simon R.12ORCID

Affiliation:

1. Lothian Birth Cohorts, Department of Psychology The University of Edinburgh Edinburgh UK

2. Scottish Imaging Network, A Platform for Scientific Excellence (SINAPSE) Collaboration Edinburgh UK

3. Centre for Clinical Brain Sciences University of Edinburgh UK

4. Ageing and Health Research Group, Usher Institute University of Edinburgh UK

5. Alzheimer Scotland Dementia Research Centre University of Edinburgh UK

6. Department of Psychology University of Texas Austin Texas USA

Abstract

AbstractGene expression varies across the brain. This spatial patterning denotes specialised support for particular brain functions. However, the way that a given gene's expression fluctuates across the brain may be governed by general rules. Quantifying patterns of spatial covariation across genes would offer insights into the molecular characteristics of brain areas supporting, for example, complex cognitive functions. Here, we use principal component analysis to separate general and unique gene regulatory associations with cortical substrates of cognition. We find that the region‐to‐region variation in cortical expression profiles of 8235 genes covaries across two major principal components: gene ontology analysis suggests these dimensions are characterised by downregulation and upregulation of cell‐signalling/modification and transcription factors. We validate these patterns out‐of‐sample and across different data processing choices. Brain regions more strongly implicated in general cognitive functioning (g; 3 cohorts, total meta‐analytic N = 39,519) tend to be more balanced between downregulation and upregulation of both major components (indicated by regional component scores). We then identify a further 29 genes as candidate cortical spatial correlates of g, beyond the patterning of the two major components (|β| range = 0.18 to 0.53). Many of these genes have been previously associated with clinical neurodegenerative and psychiatric disorders, or with other health‐related phenotypes. The results provide insights into the cortical organisation of gene expression and its association with individual differences in cognitive functioning.

Funder

Medical Research Council

National Institutes of Health

Age UK

Wellcome Trust

Publisher

Wiley

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