首页> 外文期刊>Current Microbiology >Identification of Genes Differentially Expressed by Metarhizium anisopliae Growing on Locusta migratoria Wings Using Suppression Subtractive Hybridization
【24h】

Identification of Genes Differentially Expressed by Metarhizium anisopliae Growing on Locusta migratoria Wings Using Suppression Subtractive Hybridization

机译:应用抑制消减杂交技术鉴定在南方蝗上翅膀上生长的拟南芥不同表达的基因

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

Insect-pathogenic fungi penetrate their hosts directly through the cuticle. To better understand this process, we identified genes that were up-regulated by Metarhizium anisopliae germinating and differentiating on Locusta migratoria wings using suppression subtractive hybridization (SSH). A total of 78 unique expressed sequence tags (ESTs) up-regulated more than twofold during fungal growth on locust wings were identified. Among these 78 ESTs, 30 (38.5%) shared significant similarity with NCBI annotated hypothetical proteins, 16 (20.5%) shared low similarity to known or predicted genes, might represent novel genes, and 32 (41.0%) shared significant similarity with known proteins that are involved in various cell and molecular processes such as cell metabolism, protein metabolism, stress response and defense, and cell structure and function. Semi-quantitative RT-PCR analysis of six randomly selected genes confirmed the SSH results, verifying the fidelity of the SSH data. The results of this study provide novel information on genes expressed during early stages of infection with M. anisopliae, and improve current understanding of fungal pathogenesis.
机译:病原性真菌直接通过表皮穿透宿主。为了更好地理解此过程,我们使用抑制消减杂交(SSH)鉴定了偏南异种菌上调发芽和分化的基因,而这些基因在偏斜的蝗虫翅膀上发芽并分化。在蝗虫翅膀上的真菌生长过程中,总共鉴定出总共上调两倍以上的78个独特表达序列标签(EST)。在这78个EST中,有30个(38.5%)与NCBI注释的假设蛋白具有显着相似性,有16个(20.5%)与已知或预测的基因具有低相似性,可能代表新基因,而32个(41.0%)与已知的蛋白具有显着相似性它们参与各种细胞和分子过程,例如细胞代谢,蛋白质代谢,应激反应和防御以及细胞结构和功能。对六个随机选择的基因进行的半定量RT-PCR分析证实了SSH结果,证实了SSH数据的保真度。这项研究的结果提供了新的信息有关在M.anisopliae感染的早期阶段表达的基因,并提高了目前对真菌发病机理的了解。

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