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秀丽隐杆线虫的pgp-5参与对细菌感染和重金属的抗性,其调控需要TIR-1和一个p38丝裂原活化蛋白激酶级联反应。

Caenorhabditis elegans pgp-5 is involved in resistance to bacterial infection and heavy metal and its regulation requires TIR-1 and a p38 map kinase cascade.

作者信息

Kurz C Léopold, Shapira Michael, Chen Karen, Baillie David L, Tan Man-Wah

机构信息

Department of Genetics and Department of Microbiology and Immunology, M337 Always Building, 300 Pasteur Drive, Stanford University School of Medicine, Stanford, CA 94305-5120, USA.

出版信息

Biochem Biophys Res Commun. 2007 Nov 16;363(2):438-43. doi: 10.1016/j.bbrc.2007.08.190. Epub 2007 Sep 12.

Abstract

Animals and plants respond to bacterial infections and environmental stresses by inducing overlapping repertoires of defense genes. How the signals associated with infection and abiotic stresses are differentially integrated within a whole organism remains to be fully addressed. We show that the transcription of a Caenorhabditis elegans ABC transporter, pgp-5 is induced by both bacterial infection and heavy metal stress, but the magnitude and tissue distribution of its expression differs, depending on the type of stressor. PGP-5 contributes to resistance to bacterial infection and heavy metals. Using pgp-5 transcription as a read-out, we show that signals from both biotic and abiotic stresses are integrated by TIR-1, a TIR domain adaptor protein orthologous to human SARM, and a p38 MAP kinase signaling cassette. We further demonstrate that not all the TIR-1 isoforms are necessary for nematode resistance to infection, suggesting a molecular basis for the differential response to abiotic and biotic stress.

摘要

动物和植物通过诱导重叠的防御基因库来应对细菌感染和环境胁迫。与感染和非生物胁迫相关的信号如何在整个生物体中进行差异整合仍有待充分探讨。我们发现,秀丽隐杆线虫的一种ABC转运蛋白pgp-5的转录可由细菌感染和重金属胁迫诱导,但根据胁迫源的类型,其表达的幅度和组织分布有所不同。PGP-5有助于抵抗细菌感染和重金属。以pgp-5转录作为指标,我们发现来自生物和非生物胁迫的信号由TIR-1整合,TIR-1是一种与人类SARM直系同源的TIR结构域衔接蛋白,以及一个p38丝裂原活化蛋白激酶信号盒。我们进一步证明,并非所有TIR-1同工型对线虫抗感染都是必需的,这为对非生物和生物胁迫的差异反应提供了分子基础。

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