Characterization of the promoter region, first ten exons and nine intron-exon boundaries of the DNA-dependent protein kinase catalytic subunit gene, DNA-PKcs (XRCC7)

DNA Res. 1997 Apr 28;4(2):151-4. doi: 10.1093/dnares/4.2.151.

Abstract

The gene, DNAPKcs (XRCC7), for the human DNA-dependent protein kinase catalytic subunit (DNA-PKcs) is a strong candidate that complements a severe combined immunodeficiency (scid) and hypersensitivity to ionizing radiation in mice. We constructed a cosmid library from a previously identified, X RCC7-covering YAC clone (943G4). From the library, we isolated three cosmid clones containing the 5'-region of XRCC7. Sequence analysis with primer walking on a 6.3-kb segment of these cosmids identified the promoter region, the first ten exons and nine intron-exon boundaries of XRCC7. The promoter region contains several potential Sp1 protein-binding sites and a high G+C content but no TATA or CCAAT boxes. These findings are consistent with the TATA-less housekeeping gene promoter and provides the basis for transcriptional regulatory studies. Since nine other exons spanning an 8-kb segment are already known, a total of 19 exons in the gene have been identified. The cosmids isolated and the primer sets designed in the present study are useful for mutation analysis in patients with a SCID phenotype.

MeSH terms

  • Base Sequence
  • Blotting, Southern
  • Chromosome Mapping
  • Cloning, Molecular
  • Cosmids
  • DNA, Complementary
  • DNA-Activated Protein Kinase
  • DNA-Binding Proteins*
  • Exons
  • Humans
  • Introns
  • Molecular Sequence Data
  • Nuclear Proteins
  • Promoter Regions, Genetic
  • Protein Serine-Threonine Kinases / genetics*
  • Sequence Analysis, DNA

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • Nuclear Proteins
  • DNA-Activated Protein Kinase
  • PRKDC protein, human
  • Protein Serine-Threonine Kinases