Identification of novel lung genes in bronchial epithelium by serial analysis of gene expression

Am J Respir Cell Mol Biol. 2006 Dec;35(6):651-61. doi: 10.1165/rcmb.2006-0056OC. Epub 2006 Jun 29.

Abstract

A description of the transcriptome of human bronchial epithelium should provide a basis for studying lung diseases, including cancer. We have deduced global gene expression profiles of bronchial epithelium and lung parenchyma, based on a vast dataset of nearly two million sequence tags from 21 serial analysis of gene expression (SAGE) libraries from individuals with a history of smoking. Our analysis suggests that the transcriptome of the bronchial epithelium is distinct from that of lung parenchyma and other tissue types. Moreover, our analysis has identified novel bronchial-enriched genes such as MS4A8B, and has demonstrated the use of SAGE for the discovery of novel transcript variants. Significantly, gene expression associated with ciliogenesis is evident in bronchial epithelium, and includes the expression of transcripts specifying axonemal proteins DNAI2, SPAG6, ASP, and FOXJ1 transcription factor. Moreover, expression of potential regulators of ciliogenesis such as MDAC1, NYD-SP29, ARMC3, and ARMC4 were also identified. This study represents a comprehensive delineation of the bronchial and parenchyma transcriptomes, identifying more than 20,000 known and hypothetical genes expressed in the human lung, and constitutes one of the largest human SAGE studies reported to date.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Bronchi / drug effects
  • Bronchi / metabolism*
  • Cilia / drug effects
  • Cilia / metabolism
  • Cluster Analysis
  • Databases, Nucleic Acid
  • Expressed Sequence Tags
  • Gene Expression Profiling*
  • Gene Library
  • Humans
  • Lung / drug effects
  • Lung / metabolism*
  • Middle Aged
  • Nicotiana*
  • Oligonucleotide Array Sequence Analysis
  • Pulmonary Surfactant-Associated Protein B / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reproducibility of Results
  • Respiratory Mucosa / drug effects*
  • Respiratory Mucosa / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Smoke / adverse effects*
  • Transcription, Genetic / drug effects*

Substances

  • Pulmonary Surfactant-Associated Protein B
  • RNA, Messenger
  • Smoke