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Regulation of processing of a plant glycoprotein in the Golgi complex: A comparative study usingXenopus oocytes.植物糖蛋白在高尔基复合体中的加工调控:使用非洲爪蟾卵母细胞的比较研究。
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Liquefaction of Autographa californica nucleopolyhedrovirus-infected insects is dependent on the integrity of virus-encoded chitinase and cathepsin genes.苜蓿银纹夜蛾核型多角体病毒感染的昆虫的液化取决于病毒编码的几丁质酶和组织蛋白酶基因的完整性。
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杆状病毒诱导的几丁质酶在昆虫细胞内质网中的定位

Localization of a baculovirus-induced chitinase in the insect cell endoplasmic reticulum.

作者信息

Thomas C J, Brown H L, Hawes C R, Lee B Y, Min M K, King L A, Possee R D

机构信息

NERC Institute of Virology and Environmental Microbiology, Oxford OX1 3SR, United Kingdom.

出版信息

J Virol. 1998 Dec;72(12):10207-12. doi: 10.1128/JVI.72.12.10207-10212.1998.

DOI:10.1128/JVI.72.12.10207-10212.1998
PMID:9811762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC110568/
Abstract

Confocal immunofluorescence microscopy was used to demonstrate that the Autographa californica nucleopolyhedrovirus (AcMNPV) chitinase was localized within the endoplasmic reticulum (ER) of virus-infected insect cells. This was consistent with removal of the signal peptide from the chitinase and an ER localization motif (KDEL) at the carboxyl end of the protein. Chitinase release from cells, a prerequisite for liquefaction of virus-infected insect larvae, appears to be aided by synthesis of the p10 protein. Deletion of p10 from the AcMNPV genome delayed the appearance of chitinase activity in the medium of virus-infected cells by 24 h and also delayed liquefaction of virus-infected Trichoplusia ni larvae by the same period.

摘要

共聚焦免疫荧光显微镜用于证明苜蓿银纹夜蛾核多角体病毒(AcMNPV)几丁质酶定位于病毒感染昆虫细胞的内质网(ER)中。这与几丁质酶信号肽的去除以及该蛋白质羧基末端的内质网定位基序(KDEL)一致。几丁质酶从细胞中释放是病毒感染昆虫幼虫液化的前提条件,这似乎得益于p10蛋白的合成。从AcMNPV基因组中删除p10会使病毒感染细胞培养基中几丁质酶活性的出现延迟24小时,同时也会使病毒感染的粉纹夜蛾幼虫的液化延迟相同时间。