In order to clarify the cause of null mutations in enzyme loci, the molecular structure of six null mutations in the Gpdh locus (encoding αGPBH: α 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. © The Genetical Society of Great Britain.
CITATION STYLE
Yamaguchi, Y., Takano, T. S., Yamazaki, T., & Harada, K. (1994). Molecular analysis of Gpdh null mutations that arose in mutation accumulation experiments in Drosophila melanogaster. Heredity, 73(4), 397–404. https://doi.org/10.1038/hdy.1994.187
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