Differential Expression Pattern of Heat Shock Protein Genes in Toxigenic and Atoxigenic Isolate of Aspergillus flavus

R. Thakur, S. Tiwari, J. Shankar
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引用次数: 4

Abstract

Aflatoxin biosynthesis in Aspergillus flavus requires coordinated expression of regulatory and structural genes. Aflatoxin production is optimum at 24-30°C and inhibition occurs at temperature higher than 35°C. Chaperones or heat-sock proteins are involved in processing of cellular protein and heat-stress induced protein, hence, we studied the genes encoding for heat-shock proteins under the influence of temperature (30°C vs. 37°C). A. flavus isolates, aflatoxigenic (MTCC9367) and atoxigenic (MTCC11580) were grown in glucose minimal salt broth for 24 hours for expression profile of selected genes using quantitative real-time PCR. We monitored the expression profile of genes encoding for heat-shock proteins ( hsp98, hsp90 , hsp70 and hsp60 ) and regulatory gene of aflatoxin biosynthesis pathway aflR . We found the similar trend for heat-shock proteins gene expression except hsp70 in aflatoxigenic and atoxigenic isolates of A. flavus . Expression for hsp70 was found to be upregulated at 30°C (vs 37°C)in atox igenic isolate ( P<0.001) of A. flavus in
黄曲霉产毒分离物和产氧分离物热休克蛋白基因的差异表达模式
黄曲霉毒素的合成需要调控基因和结构基因的协调表达。黄曲霉毒素的最佳产生温度为24-30°C,抑制温度高于35°C。伴侣蛋白或热袜蛋白参与细胞蛋白和热应激诱导蛋白的加工,因此,我们研究了温度(30°C vs. 37°C)影响下热休克蛋白的编码基因。将黄曲霉致黄曲霉毒素(MTCC9367)和抗氧毒素(MTCC11580)分离株在葡萄糖微盐培养液中培养24小时,利用实时荧光定量PCR检测所选基因的表达谱。我们检测了热休克蛋白编码基因(hsp98、hsp90、hsp70和hsp60)和黄曲霉毒素生物合成途径调控基因aflR的表达谱。在黄曲霉毒素和无氧毒素分离株中,除hsp70外,热休克蛋白基因表达趋势相似。hsp70的表达在30°C(相对于37°C)时被发现上调(P<0.001)
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