Kotera Yu, Asai Yoshika, Okano Shutaro, Tokutake Yukako, Hosomi Akira, Saito Katsuharu, Yonekura Shinichi, Katou Shinpei
Graduate School of Science and Technology, Shinshu University, Minamiminowa 8304, Nagano 399-4598, Japan.
Plant Cell Physiol. 2024 Dec 21;65(12):2054-2065. doi: 10.1093/pcp/pcae129.
The phytohormone salicylic acid (SA) regulates plant responses to various types of environmental stress, particularly pathogen infections. We previously revealed that the benzyl alcohol O-benzoyltransferase HSR201 was required for pathogen signal-induced SA synthesis, and its overexpression together with NtCNL, encoding a cinnamate-coenzyme A ligase, was sufficient for the production of significant amounts of SA in tobacco. We herein examined the subcellular localization of HSR201 and found that it fused to a yellow fluorescent protein localized in peroxisomes. Most peroxisomal matrix proteins possess peroxisomal targeting signal type-1 (PTS1) located at the extreme C-terminus or PTS2 located at the N-terminus; however, a bioinformatics analysis failed to identify similar signals for HSR201. Deletion and mutation analyses of HSR201 identified one essential (extreme C-terminal Leu460) and three important (Ile455, Ile456 and Ala459) amino acid residues for its peroxisomal localization. The virus-induced gene silencing (VIGS) of PEX5, a PTS1 receptor, but not PEX7, a PTS2 receptor, compromised the peroxisomal targeting of HSR201 in Nicotiana benthamiana. When overexpressed with NtCNL, HSR201 mutants with reduced or non-peroxisomal targeting induced lower SA levels than the wild type; however, these mutations did not affect the protein stability or activity of HSR201. VIGS of the HSR201 homolog compromised pathogen signal-induced SA accumulation in N. benthamiana, which was complemented by the HSR201 wild type, but not the mutant with non-peroxisomal targeting. These results suggest that the peroxisomal localization of HSR201 is mediated by a non-canonical PTS1 and required for SA biosynthesis.
植物激素水杨酸(SA)可调节植物对各种环境胁迫的反应,尤其是病原体感染。我们之前发现,苯甲醇O-苯甲酰基转移酶HSR201是病原体信号诱导的SA合成所必需的,并且它与编码肉桂酸辅酶A连接酶的NtCNL一起过表达足以在烟草中产生大量SA。我们在此研究了HSR201的亚细胞定位,发现它与定位于过氧化物酶体的黄色荧光蛋白融合。大多数过氧化物酶体基质蛋白在极端C末端具有1型过氧化物酶体靶向信号(PTS1)或在N末端具有PTS2;然而,生物信息学分析未能鉴定出HSR201的类似信号。HSR201的缺失和突变分析确定了其过氧化物酶体定位的一个必需氨基酸残基(极端C末端的Leu460)和三个重要氨基酸残基(Ile455、Ile456和Ala459)。1型过氧化物酶体靶向信号(PTS1)受体PEX5的病毒诱导基因沉默(VIGS),而不是2型过氧化物酶体靶向信号(PTS2)受体PEX7的沉默,损害了HSR201在本氏烟草中的过氧化物酶体靶向。当与NtCNL一起过表达时,靶向减少或无过氧化物酶体的HSR201突变体诱导的SA水平低于野生型;然而,这些突变不影响HSR201的蛋白质稳定性或活性。HSR201同源物的VIGS损害了本氏烟草中病原体信号诱导的SA积累,野生型HSR201可对其进行互补,但无过氧化物酶体靶向的突变体则不能。这些结果表明,HSR201的过氧化物酶体定位由非典型PTS1介导,并且是SA生物合成所必需的。