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家蚕中β-N-乙酰氨基葡萄糖苷酶的表达谱及启动子分析

The expression profile and promoter analysis of β-N-acetylglucosaminidases in the silkworm Bombyx mori.

作者信息

Zhai Yuan-Fen, Huang Ming-Xia, Wu Yu, Zhao Guo-Dong, Du Jie, Li Bing, Shen Wei-de, Wei Zheng-Guo

机构信息

School of Basic Medicine and Biological Sciences, Soochow University, Suzhou, 215123, Jiangsu, People's Republic of China.

出版信息

Mol Biol Rep. 2014 Oct;41(10):6667-78. doi: 10.1007/s11033-014-3550-6. Epub 2014 Jul 8.

DOI:10.1007/s11033-014-3550-6
PMID:25001591
Abstract

β-N-acetylglucosaminidase (GlcNAcase) is a key enzyme in the chitin decomposition process. In this study, we investigated the gene expression profile of GlcNAcases and the regulation mechanism for one of these genes, BmGlcNAcase1, in the silkworm. We performed sequence analysis of GlcNAcase. Using dual-spike-in qPCR method, we examined the expression of Bombyx β-N-acetylglucosaminidases (BmGlcNAcases) in various tissues of silkworm as well as expression changes after stimulation with ecdysone. Using Bac-to-Bac system and luciferase reporter vectors, we further analyzed the promoter sequence of BmGlcNAcase1. The results showed that these proteins have a highly conserved catalytic domain. The expression levels of the BmGlcNAcase genes varied in different tissues, and were increased 48 h after exposure to ecdysone. BmGlcNAcase1 gene promoter with 5'-end serial deletions showed different levels of activity in various tissues, higher in the blood, skin and fat body. Deletion of the region from -347 to -223 upstream of BmGlcNAcase-1 gene abolished its promoter activity. This region contains the binding sites for key transcription factors including Hb, BR-C Z, the HSF and the typical TATA-box element. These results indicate that BmGlcNAcases are expressed at different levels in different tissues of the silkworm, but all are subjected to the regulation by ecdysone. BmGlcNAcase1 promoter analysis has paved a foundation for further study of the gene expression patterns.

摘要

β-N-乙酰氨基葡萄糖苷酶(GlcNAcase)是几丁质分解过程中的关键酶。在本研究中,我们调查了家蚕中GlcNAcases的基因表达谱以及其中一个基因BmGlcNAcase1的调控机制。我们对GlcNAcase进行了序列分析。使用双内参qPCR方法,我们检测了家蚕不同组织中家蚕β-N-乙酰氨基葡萄糖苷酶(BmGlcNAcases)的表达以及蜕皮激素刺激后的表达变化。利用杆状病毒表达系统和荧光素酶报告载体,我们进一步分析了BmGlcNAcase1的启动子序列。结果表明,这些蛋白质具有高度保守的催化结构域。BmGlcNAcase基因的表达水平在不同组织中有所不同,并且在暴露于蜕皮激素48小时后升高。具有5'端连续缺失的BmGlcNAcase1基因启动子在不同组织中表现出不同水平的活性,在血液、皮肤和脂肪体中活性较高。BmGlcNAcase-1基因上游-347至-223区域的缺失消除了其启动子活性。该区域包含关键转录因子Hb、BR-C Z、HSF的结合位点以及典型的TATA盒元件。这些结果表明,BmGlcNAcases在家蚕不同组织中的表达水平不同,但均受蜕皮激素调控。BmGlcNAcase1启动子分析为进一步研究该基因的表达模式奠定了基础。

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