Molecular analysis of the Neurospora clock: cloning and characterization of the frequency and period-4 genes

Chronobiol Int. 1992 Jun;9(3):231-9. doi: 10.3109/07420529209064532.

Abstract

Genetic analysis of Neurospora crassa has identified many mutants that affect the biological clock. In this article we review the cloning of two of these genes, frq and prd-4. Both genes were isolated using a chromosome walk technique. Subcloning experiments and subsequent Northern analysis of frq implicate the importance of two transcripts that emanate from this locus. In preliminary data, no protein-coding region is evident in the smaller transcript; the larger transcript contains a 962-amino acid open reading frame. The open reading frame shows limited homology to per, a clock gene identified in Drosophila. Sequence analysis of all existing frq alleles suggests that the defect in each case lies within the open reading frame. Successful cloning of the prd-4 gene required walking a distance of greater than 40 kb. A physical map of this region has been constructed using restriction analysis. The dominance-recessive relationship of prd-4 and prd-4+ was established by examining the period lengths of strains harboring a wide range of prd-4/prd-4+ nuclear ratios.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Amino Acid Sequence
  • Biological Clocks / genetics*
  • Biological Clocks / physiology
  • Chromosome Mapping
  • Cloning, Molecular
  • Fungal Proteins / genetics
  • Genes, Fungal
  • Molecular Sequence Data
  • Neurospora crassa / genetics*
  • Neurospora crassa / physiology

Substances

  • Fungal Proteins