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微阵列分析揭示了赤拟谷盗幼虫补偿半胱氨酸和丝氨酸蛋白酶抑制剂的策略。

Microarray analysis reveals strategies of Tribolium castaneum larvae to compensate for cysteine and serine protease inhibitors.

机构信息

USDA ARS Center for Grain and Animal Health Research, 1515 College Ave., Manhattan, KS 66502, USA.

出版信息

Comp Biochem Physiol Part D Genomics Proteomics. 2010 Dec;5(4):280-7. doi: 10.1016/j.cbd.2010.08.001. Epub 2010 Aug 13.

DOI:10.1016/j.cbd.2010.08.001
PMID:20855237
Abstract

The transcriptome response of Tribolium castaneum larvae to dietary protease inhibitors was evaluated by whole-genome microarray analysis. RNA was isolated from guts of larvae fed control diet (no inhibitor), or diets containing 0.1% E-64 (cysteine protease inhibitor), 5.0% soybean trypsin inhibitor (STI, serine protease inhibitor), or a combination of 0.1% E-64 and 5.0% STI. Data were analyzed by pairwise analysis, in which each inhibitor treatment group was compared to control, or ANOVA of all treatment groups. In pairwise analysis, the expression of only 253 genes was significantly altered (p<0.05) in response to STI treatment, whereas E-64 and combination treatments resulted in 1574 and 1584 differentially regulated genes. The data indicate that treatments containing E-64, whether alone or in combination, significantly impacts gene expression in T. castaneum larvae. ANOVA analysis revealed 2175 genes differentially expressed in inhibitor-treated larvae compared to control (p<0.05), including genes related to proteases that were mostly up-regulated, namely cathepsins B and L, chymotrypsins, and nonproteolytic cysteine cathepsin or serine protease homologs. Inhibitor treatments induced the differential expression of other gut-related genes, as well as genes encoding proteins of unknown function. These data suggest that T. castaneum larvae compensate for dietary cysteine protease inhibitors by altering large-scale gene expression patterns.

摘要

利用全基因组微阵列分析评估了膳食蛋白酶抑制剂对赤拟谷盗幼虫转录组的应答。从摄食对照饮食(无抑制剂)、含 0.1%E-64(半胱氨酸蛋白酶抑制剂)、5.0%大豆胰蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)或 0.1%E-64 和 5.0%STI 混合物的饮食的幼虫中分离出 RNA。通过两两比较分析(其中将每个抑制剂处理组与对照组进行比较)或所有处理组的 ANOVA 分析来分析数据。在两两比较分析中,仅 STI 处理导致 253 个基因的表达发生显著改变(p<0.05),而 E-64 和组合处理则导致 1574 和 1584 个差异调节基因。数据表明,含有 E-64 的处理,无论是单独使用还是组合使用,都会显著影响赤拟谷盗幼虫的基因表达。ANOVA 分析显示,与对照相比,抑制剂处理的幼虫中有 2175 个基因表达差异(p<0.05),包括大多数上调的蛋白酶相关基因,即组织蛋白酶 B 和 L、糜蛋白酶和非蛋白酶半胱氨酸组织蛋白酶或丝氨酸蛋白酶同源物。抑制剂处理诱导了其他与肠道相关的基因以及编码未知功能蛋白的基因的差异表达。这些数据表明,赤拟谷盗幼虫通过改变大规模的基因表达模式来补偿膳食半胱氨酸蛋白酶抑制剂。

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