首页> 外文期刊>Plant Molecular Biology >Subtractive cDNA libraries identify differentially expressed genes in dormant and growing buds of leafy spurge (Euphorbia esula)
【24h】

Subtractive cDNA libraries identify differentially expressed genes in dormant and growing buds of leafy spurge (Euphorbia esula)

机译:减性cDNA文库鉴定了叶状大戟(大戟)的休眠和生长芽中差异表达的基因

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Two subtractive cDNA libraries were developed to study genes associated with bud dormancy (reverse library) and initiation of shoot growth (forward library) in leafy spurge. To identify unique sequences represented in each library, 15744 clones were screened to reduce the level of redundancy within both libraries. A total of 516 unique sequences were obtained from 2304 minimally redundant clones. Radioactive probes developed from RNAs extracted from crown buds of either intact (para-dormant control) or a series of growth-induced (2 h, 2, and 4 d after decapitation) plants were used to identify differentially expressed genes by macroarray analysis. Semi-quantitative RT-PCR was used to confirm results obtained by macroarray analysis and to determine the expression profiles for other transcripts identified within the subtractive libraries. Selected clones were also used to examine gene expression in crown buds after growth induction and/or during normal seasonal growth. In this study, four distinct patterns of gene expression were observed during the transition from para-dormancy to growth-induction. Many of the differentially regulated genes identified have unknown or hypothetical functions while others are known to play important roles in molecular functions. Gene ontology analysis identified a greater proportion of genes involved with catalytic activity in the forward library while the reverse library had a greater proportion of genes involved in DNA/RNA binding.
机译:开发了两个减性cDNA文库,以研究与叶休眠中的芽休眠(逆向文库)和芽生长的启动(正向文库)相关的基因。为了鉴定每个文库中代表的独特序列,筛选了15744个克隆以降低两个文库中的冗余水平。从2304个最小冗余克隆中总共获得516个独特序列。从完整的(准休眠控制)或一系列生长诱导的(断头后2 h,2和4 d)植物的冠芽提取的RNA中开发的放射性探针用于通过大阵列分析鉴定差异表达的基因。半定量RT-PCR用于确认通过宏阵列分析获得的结果,并确定在扣除文库中鉴定的其他转录本的表达谱。选定的克隆也用于检测生长诱导后和/或正常季节生长过程中冠芽中的基因表达。在这项研究中,从超休眠到生长诱导的过渡过程中观察到了四种不同的基因表达模式。鉴定出的许多差异调节基因具有未知或假设的功能,而已知其他一些在分子功能中起重要作用。基因本体分析发现在正向文库中有较大比例的基因涉及催化活性,而反向文库中有较大比例的基因涉及DNA / RNA结合。

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