首页> 外文学位 >Characterization of cDNA and genomic clones for a palmitoyl-acyl carrier protein thioesterase (FatB1) and an osmotin-like PR5 protein in Gossypium hirsutum.
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Characterization of cDNA and genomic clones for a palmitoyl-acyl carrier protein thioesterase (FatB1) and an osmotin-like PR5 protein in Gossypium hirsutum.

机译:陆地棉中棕榈酰基-酰基载体蛋白硫酯酶(FatB1)和渗透压样PR5蛋白的cDNA和基因组克隆的表征。

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摘要

Putative cotton cDNA clones and cognate genomic clones for a palmitoyl-acyl carrier protein (ACP) thioesterase (PATE) and an osmotin-like pathogenesis-related 5 (PR5) protein have been isolated and characterized. PATE is a class B fatty acid thioesterase with specificity for saturated long-chain fatty acids such as palmitate, and is implicated as a key enzyme to be targeted for regulation of fatty acid synthesis in order to alter cotton seed oil profiles. A nearly full-length 1.7-kb cDNA clone was isolated using a hybridization probe derived from an Arabidopsis PATE cDNA clone designated TE 3-2. A 17-kb genomic segment encompassing the PATE gene was also isolated, which has six exons and five introns with high sequence identity with other FatB cDNA/gene sequences. The deduced PATE preprotein amino acid sequence of 413 residues has putative signal sequences for targeting to the chloroplast stroma. PR5 proteins called osmotins are made in response to fungal pathogen stress or osmotic stress (water deprivation or salt exposure). Osmotins may actually form pores in fungal membranes, leading to osmotic rupture and destruction of the fungal cells. A cotton osmotin-like PR5 cDNA insert of 1,052 base-pairs was isolated and shown to encode a preprotein of 242 amino acids and is predicted to be secreted to the extracellular matrix as a neutral isoform. The deduced amino acid sequence has 16 cysteine residues that are highly conserved in osmotin-like proteins and are important in stabilizing the three-dimensional structure seen in thaumatin, zeamatin, and PR5-d. The intronless cognate cotton genomic clone has two putative ethylene response elements (GCC boxes) found in other PR5 gene promoter regions, as well as several tentative promoter/enhancer elements possibly involved in spatial/temporal gene expression.
机译:分离和鉴定了棕榈酰-酰基载体蛋白(ACP)硫酯酶(PATE)的假定棉花cDNA克隆和同源基因组克隆,以及与渗透素样致病相关的5(PR5)蛋白。 PATE是对饱和长链脂肪酸(如棕榈酸酯)具有特异性的B类脂肪酸硫酯酶,被认为是调控脂肪酸合成以改变棉籽油形态的关键酶。使用衍生自命名为TE 3-2的拟南芥PATE cDNA克隆的杂交探针分离出近乎全长的1.7-kb cDNA克隆。还分离了一个包含PATE基因的17kb基因组片段,该片段具有六个外显子和五个内含子,与其他FatB cDNA /基因序列具有高度的序列同一性。推导的413个残基的PATE前蛋白氨基酸序列具有用于靶向叶绿体基质的推定信号序列。 PR5蛋白称为渗透素是响应真菌病原体胁迫或渗透胁迫(水分缺乏或盐分暴露)而产生的。渗透素实际上可以在真菌膜上形成孔,导致渗透破裂和破坏真菌细胞。分离到1,052个碱基对的棉渗透压样PR5 cDNA插入片段,显示其编码了242个氨基酸的前蛋白,并被预测以中性同种型形式分泌到细胞外基质中。推导的氨基酸序列具有16个半胱氨酸残基,这些残基在渗透压样蛋白中高度保守,对于稳定在thaumatin,zeamatin和PR5-d中可见的三维结构非常重要。无内含子同源棉花基因组克隆具有在其他PR5基因启动子区域中发现的两个推定的乙烯反应元件(GCC盒),以及可能与时空基因表达有关的几个试探性启动子/增强子元件。

著录项

  • 作者

    Yoder, David W.;

  • 作者单位

    University of North Texas.;

  • 授予单位 University of North Texas.;
  • 学科 Biology Molecular.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 114 p.
  • 总页数 114
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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