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Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes

Abstract

Sliding between adjacent microtubules within the axonema gives rise to the motility of cilia and flagella. The driving force is produced by dynein complexes which are mainly composed of the axonemal dynein heavy chains. We used cells of human respiratory epithelium after in vitro ciliogenesis to clone cDNA fragments of nine dynein heavy chain genes, one of which had never been identified before. Dynein heavy chains are highly conserved from protozoa to human and the evolutionary ancestry of these dynein heavy chain cDNA fragments was deduced by phylogenetic analysis. These dynein heavy chain cDNAs are highly transcribed in human tissues containing axonema such as trachea, testis and brain, but not in adult heart or placenta. PAC clones containing dynein heavy chains were obtained and used to determine by FISH their chromosomal position in the human genome. They were mapped to 2p12–p11, 2q33, 3p21.2–p21.1, 13q14, 16p12 and 17p12. The chromosomal assignment of these dynein heavy chain genes which was confirmed by GeneBridge 4 radiation hybrid screening, will be extremely useful for linkage analysis efforts in patients with primary ciliary dyskinesia (PCD).

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Correspondence to Patrice Bouvagnet.

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Maiti, A., Mattéi, MG., Jorissen, M. et al. Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes. Eur J Hum Genet 8, 923–932 (2000). https://doi.org/10.1038/sj.ejhg.5200555

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  • DOI: https://doi.org/10.1038/sj.ejhg.5200555

Keywords

  • chromosomal mapping
  • human
  • dynein
  • heavy chain
  • primary ciliary dyskinesia
  • evolution

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