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链格孢菌102的β-1,3-、1,6-葡聚糖激发子诱导的IV类几丁质酶NtChitIV的特性:水杨酸和茉莉酸甲酯对NtChitIV诱导的拮抗作用

Characterization of NtChitIV, a class IV chitinase induced by beta-1,3-, 1,6-glucan elicitor from Alternaria alternata 102: Antagonistic effect of salicylic acid and methyl jasmonate on the induction of NtChitIV.

作者信息

Shinya Tomonori, Hanai Kazunari, Gális Ivan, Suzuki Kaoru, Matsuoka Ken, Matsuoka Hideaki, Saito Mikako

机构信息

Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, 2-24-16, Koganei, Tokyo 184-8588, Japan.

出版信息

Biochem Biophys Res Commun. 2007 Feb 9;353(2):311-7. doi: 10.1016/j.bbrc.2006.12.009. Epub 2006 Dec 8.

Abstract

Tobacco BY-2 class IV chitinases (TBC-1, TBC-3) were rapidly and transiently induced by the beta-1,3-, 1,6-glucan elicitor from Alternaria alternata 102 (AaGlucan). The full-length cDNA and 5'-flanking region of a gene encoding class IV chitinases were isolated on the basis of the amino acid sequence of TBC-1. Sequence analysis indicated that NtChitIV encoded TBC-1, TBC-3, or both. Since purified TBC-1 and TBC-3 from BY-2 cells lack a chitin binding domain in the N-terminal region, these enzymes suggested to be derived from NtChitIV by post-translational proteolytic processing. The transcripts of NtChitIV accumulated rapidly within 1h after treatment with AaGlucan. Accumulation was maximal 3h after treatment. Reporter gene assays were used to analyze the promoter regions involved in the transcriptional control of NtChitIV, and these assays revealed that the 1.89-kb NtChitIV promoter was activated by AaGlucan but not by salicylic acid (SA) or methyl jasmonate (MeJA). The AaGlucan-induced transcriptional activation via 1.89-kb NtChitIV promoter was attenuated by pretreatment with SA or MeJA. These results suggest that NtChitIV expression is particularly induced by AaGlucan and that the AaGlucan-dependent signaling pathway is different from the SA- and MeJA-dependent signaling pathways.

摘要

烟草BY-2 IV类几丁质酶(TBC-1、TBC-3)可被来自链格孢菌102(AaGlucan)的β-1,3-、1,6-葡聚糖激发子快速且短暂地诱导。基于TBC-1的氨基酸序列,分离出了编码IV类几丁质酶的基因的全长cDNA和5'-侧翼区。序列分析表明,NtChitIV编码TBC-1、TBC-3或两者。由于从BY-2细胞中纯化得到的TBC-1和TBC-3在N端区域缺乏几丁质结合结构域,这些酶推测是通过翻译后蛋白水解加工从NtChitIV衍生而来。用AaGlucan处理后1小时内,NtChitIV的转录本迅速积累。处理后3小时积累量达到最大。采用报告基因分析来分析参与NtChitIV转录调控的启动子区域,这些分析表明1.89 kb的NtChitIV启动子被AaGlucan激活,但不被水杨酸(SA)或茉莉酸甲酯(MeJA)激活。通过SA或MeJA预处理可减弱AaGlucan经由1.89 kb NtChitIV启动子诱导的转录激活。这些结果表明,NtChitIV的表达特别受AaGlucan诱导,且AaGlucan依赖的信号通路不同于SA和MeJA依赖的信号通路。

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