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海藻糖-6-磷酸合酶和海藻糖酶基因的 RNA 干扰调节豌豆蚜两种体色型的几丁质代谢。

RNA interference of trehalose-6-phosphate synthase and trehalase genes regulates chitin metabolism in two color morphs of Acyrthosiphon pisum Harris.

机构信息

College of Plant Protection, Gansu Agricultural University, Lanzhou, 730070, Gansu, China.

Biocontrol Engineering Laboratory of Crop Diseases and Pests of Gansu Province, Lanzhou, 730070, Gansu, China.

出版信息

Sci Rep. 2021 Jan 13;11(1):948. doi: 10.1038/s41598-020-80277-2.

DOI:10.1038/s41598-020-80277-2
PMID:33441844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7806880/
Abstract

Trehalose-6-phosphate synthase (TPS) and trehalase (TRE) directly regulate trehalose metabolism and indirectly regulate chitin metabolism in insects. Real-time quantitative PCR (RT-qPCR) and RNA interference (RNAi) were used to detect the expressions and functions of the ApTPS and ApTRE genes. Abnormal phenotypes were found after RNAi of ApTRE in the Acyrthosiphon pisum. The molting deformities were observed in two color morphs, while wing deformities were only observed in the red morphs. The RNAi of ApTPS significantly down-regulated the expression of chitin metabolism-related genes, UDP-N-acetyglucosamine pyrophosphorylase (ApUAP), chitin synthase 2 (Apchs-2), Chitinase 2, 5 (ApCht2, 5), endo-beta-N-acetylglucosaminidase (ApENGase) and chitin deacetylase (ApCDA) genes at 24 h and 48 h; The RNAi of ApTRE significantly down-regulated the expression of ApUAP, ApCht1, 2, 8 and ApCDA at 24 h and 48 h, and up-regulated the expression of glucose-6-phosphate isomerase (ApGPI) and Knickkopf protein (ApKNK) genes at 48 h. The RNAi of ApTRE and ApTPS not only altered the expression of chitin metabolism-related genes but also decreased the content of chitin. These results demonstrated that ApTPS and ApTRE can regulate the chitin metabolism, deepen our understanding of the biological functions, and provide a foundation for better understanding the molecular mechanism of insect metamorphosis.

摘要

海藻糖-6-磷酸合酶 (TPS) 和海藻糖酶 (TRE) 直接调节海藻糖代谢,并间接调节昆虫中的几丁质代谢。实时定量 PCR (RT-qPCR) 和 RNA 干扰 (RNAi) 用于检测 ApTPS 和 ApTRE 基因的表达和功能。在 RNAi 干扰豌豆蚜 ApTRE 后,发现其出现了异常表型。在两种颜色形态中观察到蜕皮畸形,而仅在红色形态中观察到翅膀畸形。ApTPS 的 RNAi 显著下调了几丁质代谢相关基因的表达,包括 UDP-N-乙酰葡萄糖胺焦磷酸化酶 (ApUAP)、几丁质合成酶 2 (Apchs-2)、几丁质酶 2、5 (ApCht2、5)、内-β-N-乙酰葡糖胺酶 (ApENGase) 和几丁质脱乙酰酶 (ApCDA),在 24 h 和 48 h 时;ApTRE 的 RNAi 显著下调了 ApUAP、ApCht1、2、8 和 ApCDA 在 24 h 和 48 h 的表达,并在 48 h 时上调了葡萄糖-6-磷酸异构酶 (ApGPI) 和 Knickkopf 蛋白 (ApKNK) 基因的表达。ApTRE 和 ApTPS 的 RNAi 不仅改变了几丁质代谢相关基因的表达,还降低了几丁质的含量。这些结果表明,ApTPS 和 ApTRE 可以调节几丁质代谢,加深了我们对其生物学功能的理解,并为更好地理解昆虫变态的分子机制提供了基础。

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