Lee Miin-Huey, Bostock Richard M
Department of Plant Pathology, University of California, One Shields Ave, Davis, CA 95616, USA.
Curr Genet. 2006 May;49(5):309-22. doi: 10.1007/s00294-006-0059-0. Epub 2006 Feb 9.
A transformation system utilizing Agrobacterium tumefaciens was developed for targeted gene disruption in Monilinia fructicola, a fungal pathogen that causes brown rot disease of stone fruits. Transformation with a vector containing the neomycin phosphotransferase II (nptII) cassette flanked with 4 kb cutinase gene (Mfcut1) flanking sequences resulted in an average of 13 transformants per 10(5) spores. When assayed by PCR and DNA blot analyses, more than 50% of the transformants recovered had integrated in the targeted Mfcut1 locus. Both target-gene-specific and non-specific integrations carried direct (head-to-tail) repeat T-DNA integrations. Sequence analysis of these T-DNA integrations revealed that 26 bp of the T-DNA right border were missing at the junctions between direct repeats in all cases. The recombination event during non-specific T-DNA integration in this fungus was unlike that reported in Agrobacterium-mediated transformation in plants.
开发了一种利用根癌农杆菌的转化系统,用于在核果褐腐病真菌病原菌——果生链核盘菌中进行靶向基因破坏。用含有侧翼为4 kb角质酶基因(Mfcut1)侧翼序列的新霉素磷酸转移酶II(nptII)盒的载体进行转化,平均每10⁵个孢子产生13个转化体。通过PCR和DNA印迹分析检测时,回收的转化体中超过50%已整合到靶向的Mfcut1基因座中。靶基因特异性和非特异性整合均携带直接(头对尾)重复T-DNA整合。对这些T-DNA整合的序列分析表明,在所有情况下,直接重复序列之间的连接处T-DNA右边界缺失26 bp。该真菌中非特异性T-DNA整合过程中的重组事件与植物中农杆菌介导的转化所报道的不同。