help button home button
AJRCMB
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Published ahead of print on August 28, 2003, doi:10.1165/rcmb.2003-0214OC
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2003-0214OCv1
30/3/296    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shultz, M. A.
Right arrow Articles by Buckpitt, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shultz, M. A.
Right arrow Articles by Buckpitt, A. R.
American Journal of Respiratory Cell and Molecular Biology. Vol. 30, pp. 296-310, 2004
© 2004 American Thoracic Society
DOI: 10.1165/rcmb.2003-0214OC

Gene Expression Analysis in Response to Lung Toxicants

I. Sequencing and Microarray Development

Michael A. Shultz, Lu Zhang, Yi-Zhong Gu, Gregory L. Baker, Michelle V. Fannuchi, Allan M. Padua, William A. Gurske, Dexter Morin, Sharron G. Penn, Stevan B. Jovanovich, Charles G. Plopper and Alan R. Buckpitt

Global Research, Amersham Biosciences (SV) Corp., Sunnyvale; Department of Anatomy, Physiology, and Cell Biology, and Department of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, California

Address correspondence to: Michael A. Shultz, Dept. of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, CA 95616. E-mail: mashultz{at}ucdavis.edu

A key challenge in measuring gene expression changes in the lung in response to site-selective toxicants is differentiating between target and nontarget areas. The toxicity for the cytotoxicant 1-nitronaphthalene is highly localized in the airway epithelium. Target cells comprise but a fraction of the total lung cell mass; measurements from whole lung homogenates are not likely to reflect what occurs at the target site. Additionally, the use of generic microarrays to measure expression in airway epithelium may not provide a good representation of transcripts present at the site of toxic action. cDNA libraries from airway and alveolar subcompartments of rat lung were sequenced for the development of a custom microarray representative of these lung regions. We identified 7,460 nonredundant rat lung sequences. Nearly 30% of the sequences on this array are not present on the Affymetrix Rat GeneChip 230. A 20,000-element microarray was developed that delineates differences in gene expression between subcompartments. This is the first in a series of articles employing this microarray for detecting gene expression changes during acute injury produced by 1-nitronaphthalene and subsequent repair.

Abbreviations: 1-nitronaphthalene, 1-NN • ampicillin, amp • Basic Local Alignment Search Tool, BLAST • contiguous sequences, contigs • coefficient of variation, CV • expressed sequence tag, EST • glyceraldehyde-3-phosphate dehydrogenase, GAPDH • Luria Broth, LB • polymerase chain reaction, PCR • relative fluorescent unit, RFU • sodium dodecyl sulfate, SDS • saline-sodium citrate, SSC







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 2004 American Thoracic Society.