TY - JOUR
T1 - Correlated gene expression and anatomical communication support synchronized brain activity in the mouse functional connectome
AU - Mills, Brian D.
AU - Grayson, David S.
AU - Shunmugavel, Anandakumar
AU - Miranda-Dominguez, Oscar
AU - Feczko, Eric
AU - Earl, Eric
AU - Neve, Kim A.
AU - Fair, Damien A.
N1 - Funding Information:
We thank Benjamin Jarrett, Martin Pike, and Alina Goncharova for their work on MRI acquisition, pipeline development, and data processing. This work was supported by the National Institutes of Health (grants R01 MH096773 and K99/R00 MH091238 to D.A.F.), R01 MH105538 to D.A.F.), the Oregon Clinical and Translational Research Institute (D.A.F.), the Gates Foundation (D.A.F.), the Destafano Innovation Fund (D.A.F.), a OHSU Fellowship for Diversity and Inclusion in Research Program (O.M.-D.), and a National Library of Medicine Postdoctoral Fellowship (E.F.). The authors declare no competing financial interests.
Publisher Copyright:
© 2018 the authors.
PY - 2018/6/20
Y1 - 2018/6/20
N2 - Cognition and behavior depend on synchronized intrinsic brain activity that is organized into functional networks across the brain. Research has investigated how anatomical connectivity both shapes and is shaped by these networks, but not how anatomical connectivity interacts with intra-areal molecular properties to drive functional connectivity. Here, we present a novel linear model to explain functional connectivity by integrating systematically obtained measurements of axonal connectivity, gene expression, and resting-state functional connectivity MRI in the mouse brain. The model suggests that functional connectivity arises from both anatomical links and inter-areal similarities in gene expression. By estimating these effects, we identify anatomical modules in which correlated gene expression and anatomical connectivity support functional connectivity. Along with providing evidence that not all genes equally contribute to functional connectivity, this research establishes new insights regarding the biological underpinnings of coordinated brain activity measured by BOLD fMRI.
AB - Cognition and behavior depend on synchronized intrinsic brain activity that is organized into functional networks across the brain. Research has investigated how anatomical connectivity both shapes and is shaped by these networks, but not how anatomical connectivity interacts with intra-areal molecular properties to drive functional connectivity. Here, we present a novel linear model to explain functional connectivity by integrating systematically obtained measurements of axonal connectivity, gene expression, and resting-state functional connectivity MRI in the mouse brain. The model suggests that functional connectivity arises from both anatomical links and inter-areal similarities in gene expression. By estimating these effects, we identify anatomical modules in which correlated gene expression and anatomical connectivity support functional connectivity. Along with providing evidence that not all genes equally contribute to functional connectivity, this research establishes new insights regarding the biological underpinnings of coordinated brain activity measured by BOLD fMRI.
KW - Anatomical connectivity
KW - Connectomics
KW - Gene expression
KW - Resting state functional connectivity MRI
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U2 - 10.1523/JNEUROSCI.2910-17.2018
DO - 10.1523/JNEUROSCI.2910-17.2018
M3 - Article
C2 - 29789379
AN - SCOPUS:85050920789
SN - 0270-6474
VL - 38
SP - 5774
EP - 5787
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 25
ER -