Natsume Toyoaki, Egusa Mayumi, Kodama Motoichiro, Johnson Richard, Itoh Tateo, Itoh Yasuo
Department of Biological Sciences, Faculty of Science, Shinshu University, Asahi, Matsumoto, Nagano 390-8621, Japan.
Biosci Biotechnol Biochem. 2004 Aug;68(8):1649-56. doi: 10.1271/bbb.68.1649.
Gene targeting to knock out the activity of specific genes has become important due to recent progress in genomics research. But this technique is still unavailable for many organisms, including economically important microorganisms, due to the high background of ectopic integration during genetic transformation. Strategies to improve targeting efficiency have included manipulating the expression of genes that are involved in homologous recombination. In this study, transcription of Aspergillus nidulans uvsC was elevated using the promoter sequences of the glyceraldehyde-3-phosphate dehydrogenase and Taka-amylase A genes from A. nidulans and A. oryzea respectively. Although a several-fold increase in the efficiency of targeting was observed at 3 loci, mycelial growth was suppressed in strains that had higher levels of uvsC transcription. These results suggest that uvsC is a rate-limiting factor in gene targeting, and that the increased efficiency of this targeting is hindered by a negative effect of increased transcription on cell proliferation.
由于基因组学研究的最新进展,通过基因打靶来敲除特定基因的活性已变得至关重要。但由于遗传转化过程中异位整合的背景较高,该技术在包括经济上重要的微生物在内的许多生物体中仍然无法使用。提高打靶效率的策略包括操纵参与同源重组的基因的表达。在本研究中,分别使用来自构巢曲霉和米曲霉的甘油醛-3-磷酸脱氢酶和Taka淀粉酶A基因的启动子序列来提高构巢曲霉uvsC的转录水平。尽管在3个位点观察到打靶效率提高了几倍,但uvsC转录水平较高的菌株中菌丝体生长受到抑制。这些结果表明,uvsC是基因打靶中的一个限速因子,并且这种打靶效率的提高受到转录增加对细胞增殖的负面影响的阻碍。