Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit.
Document Type
Article
Publication Date
2006
Keywords
Animals, Ethylnitrosourea, Homozygote, Immunohistochemistry, Mice, Mice-Inbred-C57BL, Molecular-Sequence-Data, Mutagenesis, Point-Mutation, Receptors-Glycine
First Page
950
Last Page
955
JAX Source
Mamm Genome 2006 Sep; 17(9):950-5.
Abstract
Nmf11 is an N-ethyl-N-nitrosourea-induced recessive mouse mutation. In this article we show that the mutation is in the gene that encodes the glycine receptor alpha 1 subunit (Glra1). The new Glra1 mutation appears to affect glycine's inhibitory neurotransmission in the central nervous system (CNS) of the nmf11 homozygotes, which suffer from a severe startle disease-related phenotype and die by postnatal day 21. The nmf11 mutation involves a C-to-A transition of nucleotide 518, which results in the N46K substitution in the long extracellular NH(2) terminal or ligand-binding domain of the GLRA1 mature protein. The mutation does not result in reduced expression of GLRA1 at the mRNA or protein levels and the mutant glycine receptor localizes properly in synaptic sites of nmf11 homozygotes.
Recommended Citation
Traka M,
Seburn KL,
Popko B.
Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit. Mamm Genome 2006 Sep; 17(9):950-5.