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利用生物枪法对小麦叶锈菌进行瞬时表达和插入诱变

Transient expression and insertional mutagenesis of Puccinia triticina using biolistics.

作者信息

Webb Craig A, Szabo Les J, Bakkeren Guus, Garry Clarke, Staples Richard C, Eversmeyer Merle, Fellers John P

机构信息

USDA-ARS, Plant Science and Entomology Research Unit, Kansas State University, Manhattan, KS 66506-5502, USA.

出版信息

Funct Integr Genomics. 2006 Jul;6(3):250-60. doi: 10.1007/s10142-005-0009-9. Epub 2005 Nov 12.

Abstract

The fungal genus Puccinia contains more than 4,000 species. Puccinia triticina, causal agent of wheat leaf rust, is an economically significant, biotrophic basidiomycete. Little is known about the molecular biology of this group, and tools for understanding gene function have not yet been established. A set of parameters was established for the transient transformation of urediniospores. The expression of three heterologous promoters (actin, elongation factor 1-alpha, and Hss1, Heat Shock 70 protein), derived from Puccinia graminis, was evaluated along with the potential for insertional mutagenesis. The UidA (GUS) gene was used as a marker for transient expression. When transferred into P. triticina urediniospores, transient expression was observed across four helium pressures using one size of gold and three sizes of tungsten microprojectiles. Each of the three promoters displayed strong transient expression in germinated urediniospores; however, higher numbers of GUS-positive urediniospores were observed when either the actin or Hss1 promoters were used. Possible concomitant insertional mutagenesis of several avirulence genes was selected in wheat cultivars harboring the cognate resistance genes. Using a linearized cloning plasmid, stable integration into the genome was achieved as demonstrated by PCR and sequencing analysis.

摘要

柄锈菌属真菌包含4000多种。小麦叶锈病的病原菌小麦条锈菌是一种具有重要经济意义的活体营养担子菌。人们对该类群的分子生物学了解甚少,且尚未建立用于理解基因功能的工具。已为夏孢子的瞬时转化建立了一组参数。对源自禾柄锈菌的三个异源启动子(肌动蛋白、延伸因子1-α和热休克70蛋白Hss1)的表达以及插入诱变的可能性进行了评估。UidA(GUS)基因用作瞬时表达的标记。当转入小麦条锈菌夏孢子后,使用一种大小的金微粒和三种大小的钨微粒,在四个氦气压力下均观察到了瞬时表达。三个启动子在萌发的夏孢子中均表现出较强的瞬时表达;然而,当使用肌动蛋白或Hss1启动子时,观察到的GUS阳性夏孢子数量更多。在携带相关抗性基因的小麦品种中筛选出了几种无毒基因可能伴随的插入诱变。使用线性化的克隆质粒,通过PCR和测序分析证明实现了向基因组的稳定整合。

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