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在家蚕变态过程中,20-羟基蜕皮酮通过广谱复合锌指蛋白4增强几丁质酶5的表达。

20-hydroxyecdysone enhances the expression of the chitinase 5 via Broad-Complex Zinc-Finger 4 during metamorphosis in silkworm, Bombyx mori.

作者信息

Zhang X, Zheng S

机构信息

Guangzhou Key Laboratory of Insect Development Regulation and Application Research, School of Life Sciences, South China Normal University, Guangzhou, China.

出版信息

Insect Mol Biol. 2017 Apr;26(2):243-253. doi: 10.1111/imb.12288. Epub 2016 Dec 29.

DOI:10.1111/imb.12288
PMID:28032930
Abstract

Insect chitinases are hydrolytic enzymes required for the degradation of chitin. They are essential for insect moulting and metamorphosis. In this study, the regulation mechanism of a chitinase gene, Bombyx mori chitinase 5 (BmCHT5), was studied. Quantitative reverse transcription PCR (qRT-PCR) analysis showed that BmCHT5 was up-regulated during the larval-larval and larval-pupa transitions and notably induced by 20-hydroxyecdysone (20E). Analysis of the BmCHT5 promoter revealed the presence of one Bombyx mori Broad-Complex Zinc-Finger Isoform 4 (BR-C Z4), two BR-C Z2 and two ecdysone-induced protein 74A (E74A) cis-regulatory elements (CREs) that are related to 20E. qRT-PCR showed that the expression of both BmBR-C Z4 and BmBR-C Z2 during metamorphosis, and when induced by 20E, was anastomotic with the variations in BmCHT5 mRNA level. In contrast, BmE74A did not follow this trend. An electrophoretic mobility shift assay did not retrieve a binding partner for the two BR-C Z2 CREs in the BmN cell line nuclear extract, whereas BR-C Z4 CRE specifically bound to BmBR-C Z4. Besides, luciferase activity analysis confirmed that BmBR-C Z4 could enhance the activity of the BmCHT5 promoter with BR-C Z4 CRE and could not enhance the promoter activity by mutating BR-C Z4 CRE. Taken together, these data suggest that the transcription factor BmBR-C Z4 enhances the expression of BmCHT5 during metamorphosis.

摘要

昆虫几丁质酶是几丁质降解所需的水解酶。它们对昆虫蜕皮和变态至关重要。在本研究中,对一种几丁质酶基因家蚕几丁质酶5(BmCHT5)的调控机制进行了研究。定量逆转录PCR(qRT-PCR)分析表明,BmCHT5在幼虫-幼虫和幼虫-蛹转变期间上调,并受到20-羟基蜕皮激素(20E)的显著诱导。对BmCHT5启动子的分析揭示了存在一个家蚕广谱复合体锌指异构体4(BR-C Z4)、两个BR-C Z2和两个与20E相关的蜕皮激素诱导蛋白74A(E74A)顺式调控元件(CRE)。qRT-PCR表明,BmBR-C Z4和BmBR-C Z2在变态期间以及受到20E诱导时的表达与BmCHT5 mRNA水平的变化吻合。相比之下,BmE74A没有遵循这一趋势。电泳迁移率变动分析未在BmN细胞系核提取物中找到两个BR-C Z2 CRE的结合伙伴,而BR-C Z4 CRE特异性结合BmBR-C Z4。此外,荧光素酶活性分析证实,BmBR-C Z4可增强具有BR-C Z4 CRE的BmCHT5启动子的活性,而通过突变BR-C Z4 CRE则不能增强启动子活性。综上所述,这些数据表明转录因子BmBR-C Z4在变态期间增强BmCHT5的表达。

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