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调控单元的特征,调控单元控制黑化并影响蚊子的寿命。

Characterization of a regulatory unit that controls melanization and affects longevity of mosquitoes.

机构信息

Division of Biology, Kansas State University, 271 Chalmers Hall, Manhattan, KS 66506, USA.

出版信息

Cell Mol Life Sci. 2011 Jun;68(11):1929-39. doi: 10.1007/s00018-010-0543-z. Epub 2010 Oct 17.

Abstract

Melanization is an innate immune response in arthropods that encapsulates and kills invading pathogens. One of its rate-limiting steps is the activation of prophenoloxidase (PPO), which is controlled by an extracellular proteinase cascade and serpin inhibitors. The molecular composition of this system is largely unknown in mosquitoes with the exception of serpin-2 (SRPN2), which was previously identified as a key negative regulator of melanization. Using reverse genetic and biochemical techniques, we identified the Anopheles gambiae clip-serine proteinase CLIPB9 as a PPO-activating proteinase, which is inhibited by SRPN2. Double knockdown of SRPN2 and CLIPB9 reversed the pleiotrophic phenotype induced by SRPN2 silencing. This study identifies the first inhibitory serpin-serine proteinase pair in mosquitoes and defines a regulatory unit of melanization. Additionally, the interaction of CLIPB9 and SRPN2 affects the life span of adult female mosquitoes and therefore constitutes a well-defined potential molecular target for novel late-life acting insecticides.

摘要

黑化是节肢动物的一种固有免疫反应,可包裹并杀死入侵的病原体。其限速步骤之一是原酚氧化酶 (PPO) 的激活,该激活由细胞外蛋白酶级联和丝氨酸蛋白酶抑制剂控制。除丝氨酸蛋白酶抑制剂 2 (SRPN2) 外,该系统的分子组成在蚊子中基本未知,SRPN2 先前被鉴定为黑化的关键负调控因子。我们使用反向遗传学和生化技术鉴定了冈比亚按蚊的剪接丝氨酸蛋白酶 CLIPB9 是一种 PPO 激活蛋白酶,被 SRPN2 抑制。SRPN2 和 CLIPB9 的双重敲低逆转了 SRPN2 沉默引起的表型多效性。本研究鉴定了蚊子中第一个抑制性丝氨酸蛋白酶-丝氨酸蛋白酶对,并定义了黑化的调节单元。此外,CLIPB9 和 SRPN2 的相互作用影响成年雌性蚊子的寿命,因此构成了一种明确的新型晚龄作用杀虫剂的潜在分子靶标。

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