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NC-brp/brp小鼠生长分化因子5(Gdf5)基因突变的鉴定。

Identification of mutation in the growth differentiation factor 5 (Gdf5) gene in NC-brp/brp mice.

作者信息

Suto Jun-ichi

机构信息

Division of Animal Sciences, National Institute of Agrobiological Sciences, Ibaraki, Japan.

出版信息

J Vet Med Sci. 2006 Oct;68(10):1121-4. doi: 10.1292/jvms.68.1121.

Abstract

A brachypodism (brp) mutation arose spontaneously in the inbred NC mouse strain, producing a phenotype similar to that caused by bp mutation; therefore, it is strongly suggested that brp and bp are allelic. A series of bp mutations are due to defects in the growth differentiation factor 5 (Gdf5) gene. Nucleotide sequence analysis on the Gdf5 gene in NC-brp/brp mice revealed that an irregular insertion of a unit ;GGCAGCC' in exon 2 caused a frame shift leading to a premature stop codon. In addition to the known physiologic roles of brp, I found that brp significantly reduced the litter size. The brp is a novel mutant allele at the Gdf5 gene locus; I would like to name this allele Gdf5(brp).

摘要

一种短肢畸形(brp)突变在近交系NC小鼠品系中自发产生,产生的表型与bp突变所导致的表型相似;因此,强烈提示brp和bp是等位基因。一系列bp突变是由于生长分化因子5(Gdf5)基因缺陷所致。对NC-brp/brp小鼠Gdf5基因的核苷酸序列分析显示,外显子2中一个“GGCAGCC”单元的不规则插入导致了移码,从而产生一个提前终止密码子。除了brp已知的生理作用外,我发现brp显著降低了产仔数。brp是Gdf5基因座上的一个新的突变等位基因;我想将这个等位基因命名为Gdf5(brp)。

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