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果胶酸裂解酶在孢囊线虫和根结线虫诱导形成取食结构过程中的独特作用。

A distinct role of pectate lyases in the formation of feeding structures induced by cyst and root-knot nematodes.

作者信息

Wieczorek K, Elashry A, Quentin M, Grundler F M W, Favery B, Seifert G J, Bohlmann H

出版信息

Mol Plant Microbe Interact. 2014 Sep;27(9):901-12. doi: 10.1094/MPMI-01-14-0005-R.

Abstract

Pectin in the primary plant cell wall is thought to be responsible for its porosity, charge density, and microfibril spacing and is the main component of the middle lamella. Plant-parasitic nematodes secrete cell wall-degrading enzymes that macerate the plant tissue, facilitating the penetration and migration within the roots. In sedentary endoparasitic nematodes, these enzymes are released only during the migration of infective juveniles through the root. Later, nematodes manipulate the expression of host plant genes, including various cell wall enzymes, in order to induce specific feeding sites. In this study, we investigated expression of two Arabidopsis pectate lyase-like genes (PLL), PLL18 (At3g27400) and PLL19 (At4g24780), together with pectic epitopes with different degrees of methylesterification in both syncytia induced by the cyst nematode Heterodera schachtii and giant cells induced by the root-knot nematode Meloidogyne incognita. We confirmed upregulation of PLL18 and PLL19 in both types of feeding sites with quantitative reverse-transcriptase polymerase chain reaction (RT-PCR) and in situ RT-PCR. Furthermore, the functional analysis of mutants demonstrated the important role of both PLL genes in the development and maintenance of syncytia but not giant cells. Our results show that both enzymes play distinct roles in different infected root tissues as well as during parasitism of different nematodes.

摘要

植物初生细胞壁中的果胶被认为与其孔隙率、电荷密度和微纤丝间距有关,并且是胞间层的主要成分。植物寄生线虫分泌细胞壁降解酶,使植物组织浸软,便于在根内穿透和迁移。在定居型内寄生线虫中,这些酶仅在感染性幼虫穿过根的迁移过程中释放。之后,线虫操纵宿主植物基因的表达,包括各种细胞壁酶,以诱导特定的取食位点。在本研究中,我们研究了拟南芥两个果胶酸裂解酶样基因(PLL),即PLL18(At3g27400)和PLL19(At4g24780)的表达,以及在甜菜孢囊线虫诱导的合胞体和南方根结线虫诱导的巨型细胞中不同甲酯化程度的果胶表位。我们通过定量逆转录聚合酶链反应(RT-PCR)和原位RT-PCR证实了这两个基因在两种取食位点均上调。此外,突变体的功能分析表明这两个PLL基因在合胞体而非巨型细胞的发育和维持中起重要作用。我们的结果表明,这两种酶在不同的受感染根组织以及不同线虫的寄生过程中发挥着不同的作用。

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