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

6Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

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 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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free