...
首页> 外文期刊>Molecular Plant-Microbe Interactions >Gene Discovery and Gene Expression in the Rice Blast Fungus, Magnaporthe grisea: Analysis of Expressed Sequence Tags
【24h】

Gene Discovery and Gene Expression in the Rice Blast Fungus, Magnaporthe grisea: Analysis of Expressed Sequence Tags

机译:稻瘟病菌Magnaporthe grisea中的基因发现和基因表达:表达序列标签的分析

获取原文

摘要

Over 28,000 expressed sequence tags (ESTs) were produced from cDNA libraries representing a variety of growth conditions and cell types. Several Magnaporthe grisea strains were used to produce the libraries, including a nonpathogenic strain bearing a mutation in the PMK1 mitogen-activated protein kinase. Approximately 23,000 of the ESTs could be clustered into 3,050 contigs, leaving 5,127 singleton sequences. The estimate of 8,177 unique sequences indicates that over half of the genes of the fungus are represented in the ESTs. Analysis of EST frequency reveals growth and cell type-specific patterns of gene expression. This analysis establishes criteria for identification of fungal genes involved in pathogenesis. A large fraction of the genes represented by ESTs have no known function or described homologs. Manual annotation of the most abundant cDNAs with no known homologs allowed us to identify a family of metallothionein proteins present in M. grisea, Neurospora crassa , and Fusarium graminearum . In addition, multiply represented ESTs permitted the identification of alternatively spliced mRNA species. Alternative splicing was rare, and in most cases, the alternate mRNA forms were unspliced, although alternative 5′ splice sites were also observed.
机译:从cDNA文库中产生了超过28,000个表达的序列标签(EST),它们代表了多种生长条件和细胞类型。几种Magnaporthe grisea菌株用于生产文库,包括在PMK1丝裂原活化蛋白激酶中带有突变的非致病性菌株。大约23,000个EST可以聚集成3,050个重叠群,剩下5,127个单例序列。对8,177个独特序列的估计表明,在EST中代表了真菌基因的一半以上。 EST频率的分析揭示了基因表达的生长和特定于细胞类型的模式。该分析建立了鉴定参与发病机理的真菌基因的标准。 ESTs代表的大部分基因没有已知功能或描述的同源物。手动注释最丰富的cDNA,没有已知的同源物,使我们能够鉴定出存在于稻瘟病菌,克雷索氏菌和禾谷镰刀菌中的金属硫蛋白家族。此外,多重代表的EST允许鉴定交替剪接的mRNA种类。选择性剪接是罕见的,并且在大多数情况下,尽管也观察到了替代5'剪接位点,但未剪接替代mRNA形式。

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