Molecular analysis of Gpdh null mutations that arose in mutation accumulation experiments in Drosophila melanogaster

Heredity (Edinb). 1994 Oct:73 ( Pt 4):397-404. doi: 10.1038/hdy.1994.187.

Abstract

In order to clarify the cause of null mutations in enzyme loci, the molecular structure of six null mutations in the Gpdh locus (encoding alpha GPDH: alpha glycerol-3-phosphate dehydrogenase (NAD+), E.C. 1.1.1.8; map position at 2-17.8) that arose in mutation accumulation experiments was examined. A restriction map analysis showed that five of the mutations are insertional mutations whereas the sixth is a deletion. The Gpdh regions of these null mutations were then cloned and sequenced. The inserted DNA fragments are all internally deleted P elements measuring 1.1 kb in length. Two are a KP element and two others are a HP element. All the insertions occur in the region near the initiation signal of transcription. The deletion encompasses the seventh and eighth exons over a length of 1.1 kb. These results therefore indicate that the null mutation rate at the Gpdh locus is largely influenced by P elements.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cloning, Molecular
  • Drosophila melanogaster / genetics*
  • Glycerol-3-Phosphate Dehydrogenase (NAD+)
  • Glycerolphosphate Dehydrogenase / genetics*
  • Molecular Sequence Data
  • Mutation
  • Restriction Mapping

Substances

  • Glycerolphosphate Dehydrogenase
  • Glycerol-3-Phosphate Dehydrogenase (NAD+)