首页|红褐色乌苏里貉与野生型乌苏里貉Agouti基因的克隆及表达水平分析

红褐色乌苏里貉与野生型乌苏里貉Agouti基因的克隆及表达水平分析

扫码查看
本试验选取野生型乌苏里貉和红褐色乌苏里貉为研究对象,克隆得到长为395bp的Agouti基因的CDS序列,分析两种貉Agouti基因的多态性及与其它物种的同源性并利用荧光定量PCR技术对Agouti基因在2种毛色貉中的mRNA表达水平进行了分析.结果表明:红褐色乌苏里貉Agouti基因编码序列的在130 bp碱基由G突变为T,导致其编码的氨基酸由色氨酸变为甘氨酸.红褐色乌苏里貉Agouti基因编码序列与犬、家猫、黑猩猩、野猪、马、绵羊的同源性分别为99.49%,87.50%,86.47%,85.71%,85.82%,85.82%.利用SPSS软件进行独立样本t检验,结果表明Agouti基因在2种貉皮肤组织中均可稳定表达,利用F=(1+E)-△△Ct计算可知Agouti基因在红褐色乌苏里貉中的表达量是野生型乌苏里貉的1.09倍,但差异不显著(P>0.05).
Cloning and Expression Level Study on Agouti Gene in Reddish-brown Wusuli Raccoon Dog and wild-type Raccoon Dog
In this study,wild-type and reddish-brown Wusuli raccoon dogs was selected for research object,respectively.The 395 bp DNA sequence of the Agouti was cloned.The polymorphism and homology of the Raccoon dogs,wild-type Wusuli raccoon dog and the other species was analyzed.The expression level of Agouti gene was compared in the two kinds of raccoon dog.The results showed that the homologous rate in canis familiaris,felis catus,chimpanzee,sus scrofa,equus caballus and Ovis aries was 99.49 %,87.50 %,86.47 %,85.71%,85.82 %,85.82 %,respectively.The Agouti gene was high conservative in the other species.Comparing analysis revealed there is a base substitution from G to T which leads to the amino acid from tryptophan to glycine.A complete match was found in the two kinds of raccoon dog.Based on the independent-samples T test in SPSS software,the results showed that Agouti gene was stably expressed in of skintissue of reddish-brown Wusuli raccoon dog and the expression quantity of Agouti gene in reddish-brown Wusuli-raccoon dog was 1.09 times of that of wild-type Wusuli raccoon dog (F=(1+E)-△△Ct).However,there was no significant difference between them(P>0.05).

raccoon dogAgouti geneclonereal-time PCR

于衍男、孙金海

展开 >

青岛农业大学动物科技学院,山东青岛266109

Agouti基因 克隆 荧光定量PCR

国家自然科学基金

31072018

2016

青岛农业大学学报(自然科学版)
青岛农业大学

青岛农业大学学报(自然科学版)

CSTPCD
影响因子:0.37
ISSN:1674-148X
年,卷(期):2016.33(3)
  • 7