Blair W. Perry, PhD

Functional and Evolutionary Genomics

I am a post-doctoral researcher in the Kelley Lab at Washington State University and UC Santa Cruz.

My research aims to understand complex adaptations through the integration of functional, evolutionary, and population genomic analyses.

Featured Publication:

Feeding during hibernation shifts gene expression toward active season levels in brown bears (Ursus arctos).

Perry, B.W., A.L. McDonald, S. Trojahn, M.W. Saxton, E.P. Vincent, C. Lowry, B.D. Evans Hutzenbiler, O.E. Cornejo, C.T. Robbins, H.T. Jansen, and J.L. Kelley. 2023. Feeding during hibernation shifts gene expression toward active season levels in brown bears (Ursus arctos). Physiological Genomics55:9368-380. LinkPDF.

Abstract

Hibernation in bears involves a suite of metabolical and physiological changes, including the onset of insulin resistance, that are driven in part by sweeping changes in gene expression in multiple tissues. Feeding bears glucose during hibernation partially restores active season physiological phenotypes, including partial resensitization to insulin, but the molecular mechanisms underlying this transition remain poorly understood. Here, we analyze tissue-level gene expression in adipose, liver, and muscle to identify genes that respond to midhibernation glucose feeding and thus potentially drive postfeeding metabolical and physiological shifts. We show that midhibernation feeding stimulates differential expression in all analyzed tissues of hibernating bears and that a subset of these genes responds specifically by shifting expression toward levels typical of the active season. Inferences of upstream regulatory molecules potentially driving these postfeeding responses implicate peroxisome proliferator-activated receptor gamma (PPARG) and other known regulators of insulin sensitivity, providing new insight into high-level regulatory mechanisms involved in shifting metabolic phenotypes between hibernation and active states.

Illustration by Stephen Graepel