...
首页> 外文期刊>Plant Molecular Biology Reporter >Molecular Cloning and Characterisation of Genes Coding for Glycine- and Proline-Rich Proteins (GPRPs) in Soybean
【24h】

Molecular Cloning and Characterisation of Genes Coding for Glycine- and Proline-Rich Proteins (GPRPs) in Soybean

机译:大豆中富含甘氨酸和脯氨酸的蛋白质(GPRPs)的基因的分子克隆和表征

获取原文
获取原文并翻译 | 示例

摘要

Genes encoding glycine- and proline-rich proteins (GPRPs) are widely distributed in land plants, but these have been rarely characterised. In this study, a total of six GPRPs (GmGPRP1 to 6) have been identified in the soybean genome database, and full-length complementary DNA and genomic DNA sequences of GmGPRP3 and GmGPRP4 have been cloned. GmGPRP1-6 genes encoded a set of small predicted proteins (185aa) with molecular mass of 12.35–19.67 kDa and isoelectric point of 6.79–10.22. GmGPRP1-5 contained three exons and two introns with fixed occurring sites, whereas GmGPRP6 only has two exons and one intron. In the deduced GmGPRP1-5 sequences, six amino acids (glycine, proline, histidine, alanine, lysine and tyrosine) account for more than 75% of the total protein composition. GmGPRPs showed high similarity to other known GPRPs at amino acid level. Most of GPRPs had three conserved regions, including an N-terminal XYPP-repeat domain, a central hydrophobic domain containing several uninterrupted alanine residues and a C-terminal HGK-repeat region. The transcripts of GmGPRP1, 3 and 4 appeared in different organs including seedling leaves, stems and roots, flowers and developing seeds, but every gene showed a unique organ-specific expression pattern. Furthermore, the expression of GmGPRP1, 3 and 4 was significantly induced by drought, salt and cold, but repressed by abscisic acid. In silico analysis of promoter regions of these genes revealed the presence of putative abiotic-stress regulatory elements. Our data suggest GmGPRPs encoding a class of conservative XYPP-repeat proteins probably play an important role in plant development as well as in response to abiotic stresses.
机译:编码富含甘氨酸和脯氨酸的蛋白质(GPRP)的基因广泛分布在陆地植物中,但很少被表征。在这项研究中,在大豆基因组数据库中总共鉴定出六个GPRP(GmGPRP1至6),并克隆了GmGPRP3和GmGPRP4的全长互补DNA和基因组DNA序列。 GmGPRP1-6基因编码了一组小的预测蛋白(<185aa),分子量为12.35–19.67 kDa,等电点为6.79–10.22。 GmGPRP1-5包含三个外显子和两个内含子,具有固定的发生位点,而GmGPRP6仅具有两个外显子和一个内含子。在推导的GmGPRP1-5序列中,六个氨基酸(甘氨酸,脯氨酸,组氨酸,丙氨酸,赖氨酸和酪氨酸)占总蛋白质组成的75%以上。 GmGPRPs在氨基酸水平上与其他已知GPRPs具有高度相似性。大多数GPRP具有三个保守区,包括一个N端XYPP重复域,一个包含几个不间断的丙氨酸残基的中央疏水域和一个C端HGK重复域。 GmGPRP1、3和4的转录本出现在不同的器官中,包括幼苗的叶子,茎和根,花和发育中的种子,但是每个基因都表现出独特的器官特异性表达模式。此外,GmGPRP1、3和4的表达被干旱,盐和寒冷显着诱导,但被脱落酸抑制。在计算机分析这些基因的启动子区域后,发现存在假定的非生物胁迫调控元件。我们的数据表明,编码一类保守的XYPP重复蛋白的GmGPRPs可能在植物发育以及应对非生物胁迫中起重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号