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mRNA差异显示技术研究低温条件下深黄被孢霉基因的表达差异
引用本文:杨晓霞,何仕武,赵汝丽,魏云林,林连兵,季秀玲,张琦. mRNA差异显示技术研究低温条件下深黄被孢霉基因的表达差异[J]. 云南大学学报(自然科学版), 2015, 37(2): 317-322. DOI: 10.7540/j.ynu.20140499
作者姓名:杨晓霞  何仕武  赵汝丽  魏云林  林连兵  季秀玲  张琦
作者单位:1.昆明理工大学 生命科学与技术学院,云南 昆明 650500;
基金项目:国家自然科学基金(31160016,31260034);云南省应用基础研究基金(KKSA201126005);教育部回国人员科研启动基金(KKQA201226003).
摘    要:mRNA差异显示技术已经广泛应用于研究植物、动物和微生物在各种环境条件下基因的差异表达研究.研究以15℃和30℃培养的深黄被孢霉M6-22菌体为材料,利用mRNA差异显示技术研究两种培养条件下基因的表达差异.经实时荧光定量PCR验证,共获得7条差异片段,相似性搜索结果表明它们是6-磷酸葡萄糖异构酶、单糖核苷酸转运蛋白、Ras1鸟苷酸转移因子、依赖于NAD的苹果酸脱氢酶、Δ12-脂肪酸脱氢酶、CLK4关联的丝氨酸/精氨酸丰富蛋白和假定蛋白,涉及糖酵解、蛋白质修饰、信号传导、脂肪酸合成和mRNA加工等生命过程,表明深黄被孢霉M6-22低温适应性是多种途径协同调控的结果.

关 键 词:深黄被孢霉   mRNA差异显示技术   荧光定量PCR   基因表达差异   低温适应性
收稿时间:2014-09-25

Analysis of differential gene expression in Mortierella isabellina at low temperature using mRNA differential
YANG Xiao-xia,HE Shi-wu,ZHAO Ru-li,WEI Yun-lin,LIN Lian-bing,JI Xiu-ling,ZHANG Qi. Analysis of differential gene expression in Mortierella isabellina at low temperature using mRNA differential[J]. Journal of Yunnan University(Natural Sciences), 2015, 37(2): 317-322. DOI: 10.7540/j.ynu.20140499
Authors:YANG Xiao-xia  HE Shi-wu  ZHAO Ru-li  WEI Yun-lin  LIN Lian-bing  JI Xiu-ling  ZHANG Qi
Affiliation:1.Biotechnology Research Center,School of Life Science and Technology, Kunming University of Science and Technology,Kunming 650500,China;
Abstract:The mRNA differential display PCR is widely used to investigate the differential gene expression in response to different environments in plants, animals and microorganisms.In this study, the technique was used to analyze the differential gene expression in Mortierella isabellina strain M6-22 which was cultured at 15 ℃ and 30 ℃, respectively.The results showed that 7 fragments whose mRNA levels were increased by 2 times or more at 15 ℃ were obtained from 21 candidate fragments after verification by real-time quantitative PCR.They showed high amino acid sequence similarity to glucose-6-phosphate isomerase, sugar-nucleotide transporter, ras1 guanine nucleotide exchange factor, NAD dependent malate dehydrogenase, Δ12-fatty acid desaturase and CLK4-associating serine/arginine rich protein, being potentially involved in the life processes of glycolysis, protein modification, signal transduction, fatty acid biosynthesis and mRNA processing, et al.These results indicate that the adaptation of M. isabellina M6-22 to low temperature is a coordinate regulation of multiple pathways.
Keywords:Mortierella isabellina'')"   href="  #"  >Mortierella isabellina  mRNA differential display PCR  real-time quantitative PCR  differential gene expression  cold adaptation
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