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1 Ophthalmology, University of Iowa, Iowa City, IA, USA; Center for Bioinformatics and Computational Biology, University of Iowa, Iowa City, IA, USA
2 Internal Medicine, University of Iowa, Iowa City, IA, USA
3 Pediatrics, University of Iowa, Iowa City, IA, USA
4 Electrical and Computer Engineering, University of Iowa, Iowa City, IA, USA; Biomedical Engineering, University of Iowa, Iowa City, IA, USA; Center for Bioinformatics and Computational Biology, University of Iowa, Iowa City, IA, USA
* To whom correspondence should be addressed. E-mail: paul-mccray{at}uiowa.edu.
The airway epithelium represents an important barrier between the host and the environment. It is a first site of contact with pathogens, particulates, and other stimuli, and has evolved the means to dynamically respond to these challenges. In an effort to define the transcript profile of airway epithelia, we created and sequenced cDNA libraries from cystic fibrosis (CF) and non-CF epithelia, and human lung tissue. Sequencing of these libraries produced approximately 53,000 3 prime expressed sequence tags (ESTs). From these a non-redundant UniGene set of more than 19,000 sequences was generated. Despite the relatively small contribution of airway epithelia to the total mass of the lung, focused gene discovery in this tissue yielded novel results. The ESTs included several thousand transcripts (6,416) not previously identified from cDNA sequences as expressed in the lung. Among the abundant transcripts were several genes involved in host defense. Most importantly, the set also included 879 3 prime ESTs that appear to be novel sequences not previously represented in the NCBI UniGene collection. This UniGene set should be useful for studies of pulmonary diseases involving the airway epithelium including cystic fibrosis, respiratory infections and asthma. It also provides a reagent for large scale expression profiling.
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