Suppr超能文献

一种新的来自胶孢炭疽菌锦葵专化型的肌动蛋白相关蛋白基因显示出与孢子产生相对应的表达变化。

A novel actin-related protein gene of Colletotrichum gloeosporioides f. sp. malvae shows altered expression corresponding with spore production.

作者信息

Li J, Jin S, Hsiang T, Goodwin P

机构信息

Department of Environmental Biology, University of Guelph, N1G 2W1, Guelph, ON, Canada.

出版信息

FEMS Microbiol Lett. 2001 Apr 13;197(2):209-14. doi: 10.1111/j.1574-6968.2001.tb10605.x.

Abstract

A novel actin-related protein (arp) was found in the plant pathogenic fungus, Colletotrichum gloeosporioides f. sp. malvae (Cgm), which causes anthracnose disease of round-leaved mallow (Malva pusilla). Sequence comparisons showed that this gene, arpA, belongs to the highly divergent 'other arps' category in the current arp classification system. ArpA is most similar to the arp11 gene of Mus musculus but has a unique structure with deletions at the C-terminus similar to that of the arp10 gene of Saccharomyces cerevisiae. A portion of another putative arp gene, arpB, was found immediately downstream of arpA. Expression of arpA was compared to the constitutively expressed Cgm actin gene, actA. In culture, the relative expression of arpA increased when growth conditions favored sporulation. During infection, arpA expression was greatest at the late necrotrophic phase, when sporulation occurred. Arps have been shown to be important in nuclear migration in fungal hyphae, and the expression pattern of arpA indicates that it may have a particular role during sporulation.

摘要

在植物病原真菌胶孢炭疽菌锦葵专化型(Cgm)中发现了一种新的肌动蛋白相关蛋白(arp),该真菌会引发圆叶锦葵(Malva pusilla)的炭疽病。序列比较表明,这个名为arpA的基因在当前的arp分类系统中属于高度分化的“其他arp”类别。ArpA与小家鼠的arp11基因最为相似,但具有独特的结构,其C端存在缺失,这与酿酒酵母的arp10基因类似。在arpA的紧邻下游发现了另一个假定的arp基因arpB的一部分。将arpA的表达与组成型表达的Cgm肌动蛋白基因actA进行了比较。在培养过程中,当生长条件有利于孢子形成时,arpA的相对表达量增加。在感染期间,arpA的表达在坏死营养后期(即发生孢子形成时)最高。已证明arp在真菌菌丝的核迁移中很重要,arpA的表达模式表明它在孢子形成过程中可能具有特定作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验