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首页> 外文期刊>The Journal of Veterinary Medical Science >Rolling Nagoya Mouse Strain (PROD-rol/rol) with Classic Piebald Mutation
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Rolling Nagoya Mouse Strain (PROD-rol/rol) with Classic Piebald Mutation

机译:具有经典花斑突变的滚动名古屋小鼠品系(PROD-rol / rol)

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References(20) Cited-By(1) Ataxic rolling Nagoya (PROD-rol/rol) mice, which carry a mutation in the α1 subunit of the Cav2.1 channel (Cacna1a) gene, were discovered in 1969. They show white spots on agouti coat and have a mutation in the piebald spotting (s) locus. However, mutation analysis of the s locus encoding the endothelin receptor type B (Ednrb) gene in PROD-rol/rol mice had not been performed. Here, we examined the genomic and mRNA sequences of the Ednrb gene in PROD-rol/rol and wild-type rolling Nagoya (PROD-s/s) and studied the expression patterns of Ednrb and Cacna1a genes in these mice in comparison with C57BL/6J mice. Polymerase chain reaction analyses revealed two silent nucleotide substitutions in the coding region and insertion of a retroposon-like element in intron 1 of the Ednrb gene. Expression analyses demonstrated similar localizations and levels of Ednrb and Cacna1a expression in the colon between PROD-rol/rol and PROD-s/s mice, but the expression levels of both genes were diminished compared with C57BL/6J mice. Microsatellite genotyping showed that at least particular regions of chromosome 14 proximal to the Ednrb locus of the PROD strain were derived from Japanese fancy piebald mice. These results indicated that PROD-rol/rol mice have two mutant genes, Ednrb and Cacna1a. As no PROD strain had an intact Ednrb gene, using congenic rolling mice would better serve to examine rolling Nagoya-type Cav2.1 channel dysfunctions.
机译:参考文献(20)被引诱人的By(1)共生滚动名古屋(PROD-rol / rol)小鼠在Cav2.1通道(Cacna1a)基因的α1亚基中携带突变,于1969年被发现。它们显示出白色斑点在刺豚鼠大衣上有花斑斑点位点的突变。但是,尚未对PROD-rol / rol小鼠中编码B型内皮素受体(Ednrb)基因的基因座进行突变分析。在这里,我们检查了PROD-rol / rol和野生型滚动名古屋(PROD-s / s)中Ednrb基因的基因组和mRNA序列,并与C57BL /相比,研究了Ednrb和Cacna1a基因在这些小鼠中的表达模式。 6J小鼠。聚合酶链反应分析显示,在编码区有两个沉默的核苷酸取代,并且在Ednrb基因的内含子1中插入了一个逆转录子样元件。表达分析表明PROD-rol / rol和PROD-s / s小鼠之间结肠中的Ednrb和Cacna1a表达水平相似,但与C57BL / 6J小鼠相比,这两个基因的表达水平均降低。微卫星基因分型显示,PROD株的Ednrb基因座附近的第14号染色体至少特定区域来自日本花式花斑小鼠。这些结果表明PROD-rol / rol小鼠具有两个突变基因Ednrb和Cacna1a。由于没有PROD菌株具有完整的Ednrb基因,因此使用转基因滚动小鼠会更好地检查滚动的名古屋型Cav2.1通道功能障碍。

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