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Research InterestsMy research interests
are in three areas: (1)
comparative
immunology and ecotoxicology, (2) evolutionary physiology, and
(3) conservation genetics of endemic and invasive species.
Tools we use range
from molecular and cellular to whole animal, spanning molecular
and quantitative genetics, genomics, and phylogenetic techniques. Our research team
includes three
1. Comparative Immunology & Ecotoxicology. With
support from NIH - National Center for
Research Resources through an
INBRE grant to UH-Manoa, we are investigating
how the air-borne oxidant pollutant ozone (O3-)
influence and promote inflammatory processes in the vertebrate lung. Ozone is a
prevalent component of photochemical smog, and many wilderness areas receive
substantial amounts of pollution from urban sources (many of the national
parks in the
Despite significant improvement in air quality in
many areas of the United States, O3- continues to be a
significant risk factor in pulmonary and cardiovascular disease in
humans (see EPA). We use both in vivo and in vitro
approaches. We are studying gene expression in the lung and heart
via microarray and RT-PCR in ApoE (-/-) knockout mice to gain a better
understanding of how O3- exposure contributes to pulmonary
and cardiac disease. This project is in collaboration with
Dr.
Ralph Shohet's team at the
University of
Hawai`i-Manoa's
JABSOM.
Ozone causes the dysregulation of more than 30 genes, many involved with
the inflammatory process (results to be presented at 2008 meeting of
Society of Toxicology). Our in vitro studies focus on
mechanisms involved with inflammatory processes in lung epithelial cells
(mouse, rat, human, and gecko). Among the processes we look at are
whether cells distinguish between O3- and other oxidants (e.g., hydrogen peroxide)
by comparing gene expression (the transcriptome) and cytokine production
(the proteome). The central experiments use
O3- to stimulate the cells and monitoring
responses, including cell viability (Alamar Blue & MTT-assays, LDH),
evidence for membrane peroxidation (ELISA), generation of reactive
oxygen species (ROS) and the antioxidant system (catalase, iNOS, SOD), and including up-regulation of heat shock protein 70
(hsp70) and cytokines (TNFa, IL-1, 4, -6, -8) (via ELISA, 1D & 2D SDS-PAGE electrophoresis, and
immunoblotting). My long-term goals are to
investigate the evolution of signaling pathways involved with inflammation of
epithelial cells of the respiratory pathway and ultimately the evolution
of signaling between innate and adaptive immune systems.
2. Evolutionary physiology. We are investigating the limits of thermal tolerance in Hawaiian
picture wing Drosophila. The evolution
of Hawaiian Drosophila represents a
large radiation across the
I maintain an active interest in the evolution of locomotor performance and activity metabolism of vertebrates and use of quantitative genetics approaches for dissecting genetic basis of complex phenotypes. My graduate studies at University of Wisconsin under Drs. Ted Garland (now Professor of Biology at University of California - Riverside) and Jack Hayes (postdoctoral fellow, now Professor of Biology at University of Nevada - Reno), focused on genetic and environmental bases of individual variation in locomotor performance (sprint running speed, swimming and running endurance) and whole-animal metabolism (basal [BMR], standard [SMR], field [FMR], maximal [VO2max]) in small vertebrates (rodents, lizards, snakes, amphibians). Since most activities that animals engage in involve locomotion (foraging, mate acquisition, defense), locomotor performance can be the object of natural selection (escape from predation), and the functional basis of locomotion is relatively well known. Therefore, these traits are important components of Darwinian fitness. Examples of the kinds of issues I have studied include: genetic bases of individual and population differences in locomotor performance, whole-animal metabolic rates, and their functional correlates; functional limits to altitude acclimation; empirical and theoretical aspects of trade-offs and constraints; evolution of endothermy. 3. Conservation and Evolutionary Genetics Projects. We are conducting three projects on genetic variation among groups of
island species.
A. The first project
seeks to test for latitudinal variation (clines) on O`ahu for the alcohol
dehydrogenase gene for the invasive fruit fly species Drosophila melanogaster. We are using a bi-phasa PCR technique to isolate alleles from samples
of flies collected from three elevational transects along the southern,
central, and northern portions of the island. This project is intended to establish baseline information about the
current geographic variation of populationos of D. melanogaster on O`ahu as we develop isofemale lines for
additional genetic inquiries.
B. A second project is
using genetic markers (RAPDS, mtDNA) to investigate population phylogeography
of introduced, and now invasive, red algae Gracilaria salicornia. This species was first introduced to
C. A third project is
looking at a proposed hybrid species between two species of native
sandalwoods. This project also
involves heavy reliance on genetic markers.
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Copyright © 2006 By Bryan Johnson. All rights reserved. |
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