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bioRxiv · 10.1101/2023.06.29.547064

Molecular Signatures of Attention Networks

Abstract

Attention network theory proposes three distinct types of attention - alerting, orienting, and control - that are supported by separate brain networks and modulated by different neurotransmitters, i.e., noradrenaline, acetylcholine, and dopamine. Here, we explore the extent of cortical, genetic, and molecular dissociation of these three attention systems using multimodal neuroimaging. We evaluated the spatial overlap between fMRI activation maps from the attention network test (ANT) and cortex-wide gene expression data from the Allen Human Brain Atlas. The goal was to identify genes associated with each of the attention networks in order to determine whether specific groups of genes were co-expressed with the corresponding attention networks. Furthermore, we analysed publicly available PET-maps of neurotransmitter receptors and transporters to investigate their spatial overlap with the attention networks. Our analyses revealed a substantial number of genes (3871 for alerting, 6905 for orienting, 2556 for control) whose cortex-wide expression co-varied with the activation maps, prioritizing several molecular functions such as the regulation of protein biosynthesis, phosphorylation, and receptor binding. Contrary to the hypothesized associations, the ANT activation maps neither aligned with the distribution of noradrenaline, acetylcholine, and dopamine receptor and transporter molecules, nor with transcriptomic profiles that would suggest clearly separable networks. Independence of the attention networks appeared additionally constrained by a high level of spatial dependency between the network maps. Future work may need to re-conceptualize the attention networks in terms of their segregation and re-evaluate the presumed independence at the neural and neurochemical level.

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Schindler, H., Jawinski, P., Arnatkeviciute, A., Markett, S.. 2023-06-29. Molecular Signatures of Attention Networks. https://doi.org/10.1101/2023.06.29.547064

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