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首页> 外文期刊>Comparative and functional genomics >Generation and Analysis of Expressed Sequence Tags fromChimonanthus praecox(Wintersweet) Flowers for Discovering Stress-Responsive and Floral Development-Related Genes
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Generation and Analysis of Expressed Sequence Tags fromChimonanthus praecox(Wintersweet) Flowers for Discovering Stress-Responsive and Floral Development-Related Genes

机译:蜡梅花表达序列标签的产生和分析,用于发现胁迫响应和花卉发育相关基因

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A complementary DNA library was constructed from the flowers ofChimonanthus praecox, an ornamental perennial shrub blossoming in winter in China. Eight hundred sixty-seven high-quality expressed sequence tag sequences with an average read length of 673.8 bp were acquired. A nonredundant set of 479 unigenes, including 94 contigs and 385 singletons, was identified after the expressed sequence tags were clustered and assembled. BLAST analysis against the nonredundant protein database and nonredundant nucleotide database revealed that 405 unigenes shared significant homology with known genes. The homologous unigenes were categorized according to Gene Ontology hierarchies (biological, cellular, and molecular). By BLAST analysis and Gene Ontology annotation, 95 unigenes involved in stress and defense and 19 unigenes related to floral development were identified based on existing knowledge. Twelve genes, of which 9 were annotated as “cold response,” were examined by real-time RT-PCR to understand the changes in expression patterns under cold stress and to validate the findings. Fourteen genes, including 11 genes related to floral development, were also detected by real-time RT-PCR to validate the expression patterns in the blooming process and in different tissues. This study provides a useful basis for the genomic analysis ofC. praecox.
机译:利用中国冬季开花的多年生灌木蜡梅花的花朵构建了一个互补的DNA文库。获得了867条平均阅读长度为673.8bp的高质量表达序列标签序列。在表达的序列标签被聚类和组装后,鉴定出一组非冗余的479个单基因,包括94个重叠群和385个单例。针对非冗余蛋白质数据库和非冗余核苷酸数据库的BLAST分析显示,405个单基因与已知基因具有显着的同源性。根据基因本体论层次(生物学,细胞和分子)对同源单基因进行分类。通过BLAST分析和基因本体论注释,在现有知识的基础上,鉴定出95个涉及胁迫和防御的单基因和19个与花发育相关的单基因。通过实时RT-PCR检查了12个基因,其中9个被标注为“冷应答”,以了解冷胁迫下表达模式的变化并验证发现。还通过实时RT-PCR检测了14个基因,包括与花发育有关的11个基因,以验证在开花过程和不同组织中的表达模式。该研究为C的基因组分析提供了有用的基础。 praecox。

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