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马铃薯中编码碱性几丁质酶和1,3-β-葡聚糖酶的mRNA的一级结构与表达

Primary structure and expression of mRNAs encoding basic chitinase and 1,3-beta-glucanase in potato.

作者信息

Beerhues L, Kombrink E

机构信息

Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln, Germany.

出版信息

Plant Mol Biol. 1994 Jan;24(2):353-67. doi: 10.1007/BF00020173.

Abstract

Infection of potato leaves (Solanum tuberosum L. cv. Datura) by the late blight fungus Phytophthora infestans, or treatment with fungal elicitor leads to a strong increase in chitinase and 1,3-beta-glucanase activities. Both enzymes have been implicated in the plant's defence against potential pathogens. In an effort to characterize the corresponding genes, we isolated complementary DNAs encoding the basic forms (class I) of both chitinase and 1,3-beta-glucanase, which are the most abundant isoforms in infected leaves. Sequence analysis revealed that at least four genes each are expressed in elicitor-treated leaves. The structural features of the potato chitinases include a hydrophobic signal peptide at the N-terminus, a hevein domain which is characteristic of class I chitinases, a proline- and glycine-rich linker region which varies among all potato chitinases, a catalytic domain, and a C-terminal extension. The potato 1,3-beta-glucanases also contain a N-terminal hydrophobic signal peptide and a C-terminal extension, the latter comprising a potential glycosylation site. RNA blot hybridization experiments showed that basic chitinase and 1,3-beta-glucanase are strongly and coordinately induced in leaves in response to infection, elicitor treatment, ethylene treatment, or wounding. In addition to their activation by stress, both types of genes are regulated by endogenous factors in a developmental and organ-specific manner. Appreciable amounts of chitinase and 1,3-beta-glucanase mRNAs were found in old leaves, stems, and roots, as well as in sepals of healthy, untreated plants, whereas tubers, root tips, and all other flower organs (petals, stamen, carpels) contained very low levels of both mRNAs. In young leaves and stems, chitinase and 1,3-beta-glucanase were differentially expressed. While chitinase mRNA was abundant in these parts of the plant, 1,3-beta-glucanase mRNA was absent. DNA blot analysis indicated that in potato, chitinase and 1,3-beta-glucanase are encoded by gene families of considerable complexity.

摘要

用致病疫霉感染马铃薯叶片(茄属马铃薯栽培品种曼陀罗),或用真菌激发子处理,会导致几丁质酶和1,3-β-葡聚糖酶活性大幅增加。这两种酶都与植物抵御潜在病原体有关。为了对相应基因进行表征,我们分离出了编码几丁质酶和1,3-β-葡聚糖酶基本形式(I类)的互补DNA,它们是受感染叶片中最丰富的同工型。序列分析表明,在经激发子处理的叶片中,每种酶至少有四个基因表达。马铃薯几丁质酶的结构特征包括:N端有一个疏水信号肽,一个I类几丁质酶特有的橡胶素结构域,一个在所有马铃薯几丁质酶中各不相同的富含脯氨酸和甘氨酸的连接区,一个催化结构域,以及一个C端延伸区。马铃薯1,3-β-葡聚糖酶也含有一个N端疏水信号肽和一个C端延伸区,后者包含一个潜在的糖基化位点。RNA印迹杂交实验表明,在叶片中,基本几丁质酶和1,3-β-葡聚糖酶会因感染、激发子处理、乙烯处理或创伤而被强烈且协同地诱导。除了受胁迫激活外,这两类基因还受到内源因子的调控,呈现出发育和器官特异性的方式。在老叶、茎、根以及健康未处理植株的萼片中发现了大量的几丁质酶和1,3-β-葡聚糖酶mRNA,而块茎、根尖以及所有其他花器官(花瓣、雄蕊、心皮)中这两种mRNA的含量都非常低。在幼叶和茎中,几丁质酶和1,3-β-葡聚糖酶的表达存在差异。几丁质酶mRNA在植物的这些部位含量丰富,而1,3-β-葡聚糖酶mRNA则不存在。DNA印迹分析表明,在马铃薯中,几丁质酶和1,3-β-葡聚糖酶由相当复杂的基因家族编码。

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