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The goal of my laboratory is to identify novel factors and pathways that regulate aging or age associated diseases. In this work we make use of two model systems. The first is a cross-species cell culture model. The second is genetic manipulation of the fruit fly Drosophila melanogasterWe make use of a cross-species model as there is extraordinary variation in lifespan amongst the animal kingdom. Some species will only live a few months or years while other species will live many decades. A few species can even live multiple centuries.This variation in lifespan is the product of different evolutionary pressures in different species. For instance species with few predators, a long development time and few offspring are under greater pressure to evolve strategies to slow aging rates than species with many predators, many offspring and short development times.My lab is interested in investigating factors that are enriched in species under selection for a longer lifespan. We consider this a powerful screening tool to identify factors which may be important regulators of aging. This approach has the advantage of enabling an evaluation of many factors relatively quickly without the time and cost constraints to lifespan analysis in transgenic animals.A second area of research in my lab makes use of is the fruit fly Drosophila melanogaster. This animal has powerful genetic tools which allow us to directly test whether augmentation or depletion of the factors we found to be interesting in our cross species model can slow progression of aging or age associate diseases.
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Associate ProfessorUniversity Of Alabama At BirminghamBirmingham, Al, Us -
Associate ProfessorUniversity Of Alabama At Birmingham Oct 2022 - PresentBirmingham, Alabama, United States -
Assistant ProfessorUniversity Of Alabama At Birmingham Jan 2020 - Oct 2022Birmingham, Alabama, United States -
Assistant ProfessorBarshop Institute For Longevity And Aging Studies Aug 2016 - Jan 2020San Antonio, Texas Area
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Research FellowUniversity Of Michigan Jun 2013 - Sep 2016Ann Arbor, MiPublications:Pickering AM, Lehr M, Miller RA. (2015) Lifespan of mice and primates correlates with immunoproteasome expression.J Clin Invest. May 1;125(5):2059-68. doi: 10.1172/JCI80514. Pickering, A.M., Lehr, M., Kohler, W.J., Han, M.L., and Miller, R.A. (2014). Fibroblasts from longer lived species of primates, rodents, bats, carnivores and birds resist protein damage. J Gerontol A Biol Sci Med Sci. 2014 Jul 28. pii: glu115. Funding:F-32: Comparative Cell Biology of Aging: Proteostasis Control in Long- and Short-Lived SpeciesInstitute: National institute on Aging (NIA).PI: Andrew M. Pickering. Submitted: 04/04/2014. Funding dates: 04/01/2015 – 11/31/2017Biology of Aging T-32, Institute: University of MichiganPI: Andrew M. Pickering. Funding dates: 12/01/2014 – 03/31/2015 -
Postdoctoral ScholarUcla May 2012 - Apr 2013 -
Ph.D StudentUniversity Of Southern California Aug 2007 - May 2012Los AngelesPublications:Pickering A M, Vojtovicha L, Tower J, Davies K J A. Oxidative Stress Adaption with Acute, Chronic and Repeated Stress. Free Radic Biol Med. 2013 Feb;55:109-18.Pickering A M, Staab T A, Tower J, Sieburth S, Davies K J A. A Conserved Role for the 20S Proteasome and Nrf2 Transcription Factor in Oxidative-Stress Adaptation in Mammals, C. elegans and D. melanogaster. J Exp Biol. 2013 Feb 15;216(Pt 4):543-53Pickering A M, Davies K J A. Differential roles of proteasome and immunoproteasome regulators Pa28αβ, Pa28γ and Pa200 in the degradation of oxidized proteins. Arch Biochem Biophys. 2012 Jul 15;523(2):181-90.Pickering A M, Linder RA, Zhang H, Forman H J, Davies K J A. Nrf2-dependent Induction of Proteasome and Pa28αβ Regulator Are Required for Adaptation to Oxidative Stress. J Biol Chem. 2012 Mar 23;287(13):10021-31.Pickering A M, Davies K J A. A simple fluorescence labeling method for studies of protein oxidation, protein modification, and proteolysis. FRBM. 2012 Vol. 52 (2), pp. 239-46Grune T, Catalgol B, Licht A, Ermak G, Pickering, A M, Ngo J K, Davies K J A. HSP70 mediates dissociation and reassociation of the 26S proteasome during adaptation to oxidative stress. FRBM. 2011 Vol. 51 (7), pp. 1355-64. Pickering, A. M, Koop A L, Teoh C Y, Ermak G, Grune T, Davies K J A. The immunoproteasome, the 20S proteasome, and the PA28aß proteasome regulator are oxidative stress-adaptive proteolytic complexes. Biochem J. 2010 Dec 15;432(3):585-94. Nuzhdin, S. V., Brisson, J. A., Pickering, A. M., Wayne, M. L., Harshman, L. G., McIntyre, L. M. Natural genetic variation in transcriptome reflects network structure inferred with major effect mutations: insulin/TOR and associated phenotypes in Drosophila melanogaster. BMC Genomics. 2009 Vol. 10, pp. 124. Book Chapter:Pickering A M, Davies K J A.Degradation of damaged proteins: the main function of the 20S proteasome. Prog Mol Biol Transl Sci. 2012;109:227-48
Andrew Pickering Skills
Andrew Pickering Education Details
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Molecular Biology -
Biological Sciences -
Cheadle And Marple Sixth Form CollegeHigh School -
Hillcrest Grammar SchoolHigh School
Frequently Asked Questions about Andrew Pickering
What company does Andrew Pickering work for?
Andrew Pickering works for University Of Alabama At Birmingham
What is Andrew Pickering's role at the current company?
Andrew Pickering's current role is Associate Professor.
What is Andrew Pickering's email address?
Andrew Pickering's email address is pi****@****ail.com
What is Andrew Pickering's direct phone number?
Andrew Pickering's direct phone number is +131061*****
What schools did Andrew Pickering attend?
Andrew Pickering attended University Of Southern California, Oxford University, Cheadle And Marple Sixth Form College, Hillcrest Grammar School.
What skills is Andrew Pickering known for?
Andrew Pickering has skills like Proteasome, Oxidative Stress, Cell Culture, Aging, Drosophila Melanogaster, C. Elegans, Molecular And Cellular Biology.
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