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Endochitinase gene induced by osmotic stress and abscisic acid isolated from the wild tomato Lycopersicon chilense Dun

机译:渗透胁迫和脱落酸诱导的野生番茄番茄内切酶的内切酶基因

摘要

Two osmotic stress- and ABA-responsive members of the endochitinase (EC 3.2.1.14) gene family has been isolated and identified from leaves of drought-stressed Lycopersicon chilense plants. The 966- base-pair insert of pcht28 encodes an acidic chitinase precursor with an amino-terminal signal peptide. The mature protein is predicted to have 229 amino acid residues with a relative molecular weight of 24,943 and pI value of 6.2. The same number in amino acids, molecular and PI value are predicted for the protein encoded by pchtI, despite of a slight variation in the DNA and amino acid sequences. Sequence analysis revealed that pcht28 and pchtI have a high degree of homology with class II chitinases (EC 3.2.1. 14) from tobacco. Northern blot analysis indicated that these genes have evolved a completely different pattern of expression from others reported thus far. They are highly induced by both osmotic stress and the plant hormone abscisic acid. Southern blot analysis of genomic DNA suggested that the pcht28- and pchtI-related chitinase is encoded by a small multigene family in this species. Knowing the role of plant chitinase in plant defense against fungal pathogens, it is assumed that, besides their general defensive function, the pcht28- and pchtI-encoded chitinases may play a particular role in protecting plants from pathogen attack during water stress.
机译:内切几丁质酶(EC 3.2.1.14)基因家族的两个渗透胁迫和ABA响应成员已从干旱胁迫的番茄(Lycopersicon chilense)植物的叶片中分离并鉴定出。 pcht28的966个碱基对插入片段编码带有氨基末端信号肽的酸性几丁质酶前体。预测该成熟蛋白具有229个氨基酸残基,相对分子量为24,943,pI值为6.2。尽管pchtI编码的蛋白质的氨基酸,分子和PI值相同,但DNA和氨基酸序列略有变化,但预测相同。序列分析表明,pcht28和pchtI与烟草的II类几丁质酶(EC 3.2.1。14)具有高度同源性。 Northern印迹分析表明,这些基因与迄今为止报道的其他基因已经进化出完全不同的表达模式。它们被渗透压和植物激素脱落酸强烈诱导。基因组DNA的Southern印迹分析表明,pcht28-和pchtI相关的几丁质酶由该物种中的一个小的多基因家族编码。已知植物几丁质酶在植物防御真菌病原体的防御中的作用,据推测,除了其一般的防御功能外,pcht28和pchtI编码的几丁质酶还可能在保护植物免受水分胁迫期间的病原体侵袭中发挥特殊作用。

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