The molecular genetics of alpha 1 antitrypsin deficiency

Bioessays. 1991 Apr;13(4):163-9. doi: 10.1002/bies.950130404.

Abstract

The human serum protein alpha 1-antitrypsin is the major source of antiprotease activity found in the blood. The protein is synthesised primarily by liver cells but, to a lesser extent, by at least one other cell type. Expression of the gene has provided a paradigm for studies on transcriptional regulation in liver and of tissue-specific promoter activity. The pleiomorphic nature of the gene has given rise to a variety of alpha 1-antitrypsin variants some of which are clinically important. These abnormal variants may be poorly synthesised, rapidly degraded or inefficiently secreted; studies on the molecular mechanisms which underly these events are providing interesting insights into the general processes of protein transport and intracellular protein degradation.

Publication types

  • Review

MeSH terms

  • Gene Expression Regulation
  • Genes, Regulator
  • Humans
  • Liver / physiology
  • Polymorphism, Genetic
  • Transcription, Genetic
  • alpha 1-Antitrypsin / genetics*
  • alpha 1-Antitrypsin Deficiency

Substances

  • alpha 1-Antitrypsin