Cloning of heat-shock locus 93D from Drosophila melanogaster

EMBO J. 1984 Nov;3(11):2499-504. doi: 10.1002/j.1460-2075.1984.tb02163.x.

Abstract

Using the microcloning approach a number of recombinant lambda phages carrying DNA from the 93D region have been isolated. Screening genomic libraries, cloned in phage lambda or cosmid vectors, with this isolated DNA yielded a series of overlapping DNA fragments from the region 93D6-7 as shown by in situ hybridization to polytene chromosomes. In vitro 32P-labelled nuclear RNA prepared from heat-shocked third instar larvae hybridized specifically to one fragment within 85 kb of cloned DNA. The region which is specifically transcribed after heat shock could be defined to a cluster of internally-repetitive DNA and its neighbouring proximal sequences. Over a sequence of 10-12 kb in length the DNA is cut into repeat units of approximately 280 nucleotides by the restriction endonuclease TaqI. The TaqI repeat sequences are unique in the Drosophila genome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cloning, Molecular*
  • DNA Restriction Enzymes
  • Drosophila melanogaster / genetics*
  • Genes*
  • Heat-Shock Proteins / genetics*
  • Molecular Weight
  • Nucleic Acid Hybridization
  • Plasmids
  • Repetitive Sequences, Nucleic Acid
  • Transcription, Genetic

Substances

  • Heat-Shock Proteins
  • DNA Restriction Enzymes