DNA helicases, genomic instability, and human genetic disease

Anja J. Van Brabant, Rodica Stan, Nathan A. Ellis

Research output: Contribution to journalArticlepeer-review

212 Scopus citations


DNA helicases are a highly conserved group of enzymes that unwind DNA. They function in all processes in which access to single-stranded DNA is required, including DNA replication, DNA repair and recombination, and transcription of RNA. Defects in helicases functioning in one or more of these processes can result in characteristic human genetic disorders in which genomic instability and predisposition to cancer are common features. So far, different helicase genes have been found mutated in six such disorders. Mutations in XPB and XPD can result in xeroderma pigmentosum, Cockayne syndrome, or trichothiodystrophy. Mutations in the RecQ-like genes BLM, WRN, and RECQL4 can result in Bloom syndrome, Werner syndrome, and Rothmund-Thomson syndrome, respectively. Because XPB and XPD function in both nucleotide excision repair and transcription initiation, the cellular phenotypes associated with a deficiency of each one of them include failure to repair mutagenic DNA lesions and defects in the recovery of RNA transcription after UV irradiation. The functions of the RecQ-like genes are unknown; however, a growing body of evidence points to a function in restarting DNA replication after the replication fork has become stalled. The genomic instability associated with mutations in the RecQ-like genes includes spontaneous chromosome instability and elevated mutation rates. Mouse models for nearly all of these entities have been developed, and these should help explain the widely different clinical features that are associated with helicase mutations.

Original languageEnglish (US)
Pages (from-to)409-459
Number of pages51
JournalAnnual Review of Genomics and Human Genetics
Issue number2000
StatePublished - 2000


  • Bloom syndrome
  • DNA repair and recombination
  • DNA replication
  • RecQ helicases
  • Werner syndrome
  • Xeroderma pigmentosum

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)


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