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产黄青霉和顶头孢霉中的RNA沉默:利用β-内酰胺基因表达进行的验证研究

RNA-silencing in Penicillium chrysogenum and Acremonium chrysogenum: validation studies using beta-lactam genes expression.

作者信息

Ullán Ricardo V, Godio Ramiro P, Teijeira Fernando, Vaca Inmaculada, García-Estrada Carlos, Feltrer Raúl, Kosalkova Katarina, Martín Juan F

机构信息

Institute of Biotechnology (INBIOTEC), Avda. Real no. 1, 24006 León, Spain.

出版信息

J Microbiol Methods. 2008 Oct;75(2):209-18. doi: 10.1016/j.mimet.2008.06.001. Epub 2008 Jun 12.

Abstract

In this work we report the development and validation of a new RNA interference vector (pJL43-RNAi) containing a double-stranded RNA expression cassette for gene silencing in the filamentous fungi Penicillium chrysogenum and Acremonium chrysogenum. Classical targeted gene disruption in these fungi is very laborious and inefficient due to the low frequency of homologous recombination. The RNAi vector has been validated by testing the attenuation of two different genes of the beta-lactam pathway; pcbC in P. chrysogenum and cefEF in A. chrysogenum. Quantification of mRNA transcript levels and antibiotic production showed knockdown of pcbC and cefEF genes in randomly isolated transformants of P. chrysogenum and A. chrysogenum, respectively. The process is efficient; 15 to 20% of the selected transformants were found to be knockdown mutants showing reduced penicillin or cephalosporin production. This new RNAi vector opens the way for exploring gene function in the genomes of P. chrysogenum and A. chrysogenum.

摘要

在本研究中,我们报道了一种新型RNA干扰载体(pJL43-RNAi)的构建与验证,该载体含有双链RNA表达盒,用于在丝状真菌产黄青霉和顶头孢霉中进行基因沉默。由于同源重组频率较低,在这些真菌中进行经典的靶向基因敲除非常费力且效率低下。通过检测β-内酰胺途径中两个不同基因的表达减弱情况,验证了该RNAi载体;产黄青霉中的pcbC基因和顶头孢霉中的cefEF基因。对mRNA转录水平和抗生素产量的定量分析表明,在随机分离的产黄青霉和顶头孢霉转化子中,pcbC基因和cefEF基因的表达分别受到了抑制。该方法效率较高;在所选的转化子中,有15%至20%被发现是基因表达受抑制的突变体,其青霉素或头孢菌素产量降低。这种新型RNAi载体为探索产黄青霉和顶头孢霉基因组中的基因功能开辟了道路。

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