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在辛硫磷暴露下,家蚕丝腺损伤和解毒酶相关基因的转录反应。

The silk gland damage and the transcriptional response to detoxifying enzymes-related genes of Bombyx mori under phoxim exposure.

机构信息

School of Basic Medicine and Biological Sciences, Soochow University, Suzhou, Jiangsu 215123, PR China.

School of Basic Medicine and Biological Sciences, Soochow University, Suzhou, Jiangsu 215123, PR China; National Engineering Laboratory for Modern Silk, Soochow University, Suzhou, Jiangsu 215123, PR China.

出版信息

Chemosphere. 2018 Oct;209:964-971. doi: 10.1016/j.chemosphere.2018.06.167. Epub 2018 Jun 29.

DOI:10.1016/j.chemosphere.2018.06.167
PMID:30114747
Abstract

Silk gland is a major organ of Bombyx mori for the synthesis and secretion of silk protein. Phoxim exposure can be toxic to B. mori and causes a decrease of fibroin synthesis, finally affecting the silk production in industry. To study the mechanism of metabolism and detoxification of silk gland under phoxim exposure, we measured the residual quantity of phoxim in silk gland and hemolymph after phoxim exposure, and the detoxifying enzymes-related genes and enzyme activity were also investigated. Results indicated that the residual amount of phoxim existed up to 24 h in silk gland compared with that in hemolymph, suggesting that phoxim can accumulate in the silk glands within a certain time course. The transcriptional levels of PI3K/Akt genes, including Akt, Tor1, p70s6k and 4e-bp, were up-regulated by 6.919, 1.358, 10.766 and 7.708-fold, respectively. The expression of two downstream genes (CncC and Keap1) was up-regulated by 1.939 and 3.373-fold, respectively. In addition, the transcriptional levels of detoxification-related genes including CYP6AB, CYP306A, CarE2, GST1 and GSTd1 were up-regulated by 1.731, 1.221, 1.366, 1.376 and 6.591-fold, respectively. The enzymatic activity of CYP450, CarE and GST were increased over time. These results provided possible insights into the injury of silk gland and the transcriptional response to detoxifying enzymes-related genes in silkworm after phoxim exposure.

摘要

丝腺是家蚕合成和分泌丝蛋白的主要器官。辛硫磷暴露会对家蚕产生毒性,导致丝蛋白合成减少,最终影响工业丝绸生产。为研究辛硫磷暴露下丝腺的代谢和解毒机制,我们测定了丝腺和血液中辛硫磷的残留量,同时还研究了解毒酶相关基因和酶活性。结果表明,与血液相比,丝腺中辛硫磷的残留量在 24 小时内仍然存在,这表明辛硫磷可以在一定时间内在家蚕的丝腺中积累。PI3K/Akt 基因,包括 Akt、Tor1、p70s6k 和 4e-bp 的转录水平分别上调了 6.919、1.358、10.766 和 7.708 倍。两个下游基因(CncC 和 Keap1)的表达分别上调了 1.939 和 3.373 倍。此外,解毒相关基因 CYP6AB、CYP306A、CarE2、GST1 和 GSTd1 的转录水平分别上调了 1.731、1.221、1.366、1.376 和 6.591 倍。CYP450、CarE 和 GST 的酶活性随时间增加而增加。这些结果为辛硫磷暴露后家蚕丝腺损伤和解毒酶相关基因的转录反应提供了可能的见解。

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