Network analysis identifies strain-dependent response to tau and tau seeding-associated genes

Author:

Acri Dominic J.1234ORCID,You Yanwen1256ORCID,Tate Mason D.1234ORCID,Karahan Hande1278ORCID,Martinez Pablo56ORCID,McCord Brianne1278ORCID,Sharify A. Daniel1278ORCID,John Sutha1278ORCID,Kim Byungwook1278ORCID,Dabin Luke C.1278ORCID,Philtjens Stéphanie1278ORCID,Wijeratne H.R. Sagara12910ORCID,McCray Tyler J.1234ORCID,Smith Daniel C.1234ORCID,Bissel Stephanie J.1278ORCID,Lamb Bruce T.1278ORCID,Lasagna-Reeves Cristian A.12561112ORCID,Kim Jungsu1278ORCID

Affiliation:

1. Stark Neurosciences Research Institute, Indiana University 1 , Indianapolis, IN, USA

2. School of Medicine 1 , Indianapolis, IN, USA

3. Indiana University 2 Medical Neuroscience Graduate Program, , Indianapolis, IN, USA

4. School of Medicine 2 Medical Neuroscience Graduate Program, , Indianapolis, IN, USA

5. Indiana University 3 Department of Anatomy, Cell Biology and Physiology, , Indianapolis, IN, USA

6. School of Medicine 3 Department of Anatomy, Cell Biology and Physiology, , Indianapolis, IN, USA

7. Indiana University 4 Department of Medical and Molecular Genetics, , Indianapolis, IN, USA

8. School of Medicine 4 Department of Medical and Molecular Genetics, , Indianapolis, IN, USA

9. Indiana University 5 Department of Biochemistry and Molecular Biology, , Indianapolis, IN, USA

10. School of Medicine 5 Department of Biochemistry and Molecular Biology, , Indianapolis, IN, USA

11. Center for Computational Biology and Bioinformatics, Indiana University 6 , Indianapolis, IN, USA

12. School of Medicine 6 , Indianapolis, IN, USA

Abstract

Previous research demonstrated that genetic heterogeneity is a critical factor in modeling amyloid accumulation and other Alzheimer’s disease phenotypes. However, it is unknown what mechanisms underlie these effects of genetic background on modeling tau aggregate-driven pathogenicity. In this study, we induced tau aggregation in wild-derived mice by expressing MAPT. To investigate the effect of genetic background on the action of tau aggregates, we performed RNA sequencing with brains of C57BL/6J, CAST/EiJ, PWK/PhJ, and WSB/EiJ mice (n = 64) and determined core transcriptional signature conserved in all genetic backgrounds and signature unique to wild-derived backgrounds. By measuring tau seeding activity using the cortex, we identified 19 key genes associated with tau seeding and amyloid response. Interestingly, microglial pathways were strongly associated with tau seeding activity in CAST/EiJ and PWK/PhJ backgrounds. Collectively, our study demonstrates that mouse genetic context affects tau-mediated alteration of transcriptome and tau seeding. The gene modules associated with tau seeding provide an important resource to better model tauopathy.

Funder

National Institutes of Health

Indiana University

School of Medicine, Indiana University

Indiana Clinical Translational Sciences Institute

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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