Isolation and Characterization of a Neurospora Glucose-Repressible Gene

Curr Genet. 1988 Dec;14(6):545-51. doi: 10.1007/BF00434079.

Abstract

Using differential hybridization, the cDNA copy of a Neurospora gene coding for an abundant glucose-repressible mRNA (grg-1) has been isolated. The cDNA was used to clone the genomic copy, and both were sequenced. The cDNA is nearly full length and contains putative translational start and termination codons. Conceptual translation indicates that grg-1 mRNA could direct the synthesis of a 7,000 molecular weight polypeptide. The genomic clone, contained in an 1,888 bp PvuII fragment, encompasses the entire cDNA as well as 838 bp of 5' and 369 bp of 3' flanking sequence. Comparison of the cDNA and genomic clones revealed the presence of two short introns in potential protein-coding sequences. grg-1 message levels were found to increase within minutes following the onset of glucose deprivation and rise 50 fold during the first 90 min of derepression.

Publication types

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

MeSH terms

  • Base Sequence
  • Blotting, Northern
  • Blotting, Southern
  • Cloning, Molecular
  • DNA Probes
  • DNA, Fungal / genetics
  • Gene Expression Regulation / drug effects*
  • Genes, Fungal / drug effects
  • Glucose / pharmacology*
  • Molecular Sequence Data
  • Neurospora / genetics*
  • Neurospora crassa / genetics*
  • Nucleic Acid Hybridization
  • RNA, Fungal / biosynthesis
  • RNA, Fungal / genetics
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / drug effects
  • RNA, Messenger / genetics*
  • Repressor Proteins / genetics*
  • Restriction Mapping
  • Transcription Factors / genetics*
  • Transcription, Genetic

Substances

  • DNA Probes
  • DNA, Fungal
  • RNA, Fungal
  • RNA, Messenger
  • Repressor Proteins
  • Transcription Factors
  • Glucose