Phleomycin Increases Transformation Efficiency and Promotes Single Integrations in Schizophyllum commune

被引:41
作者
van Peer, Arend F. [1 ]
de Bekker, Charissa [1 ]
Vinck, Arman [1 ]
Wosten, Han A. B. [1 ]
Lugones, Luis G. [1 ]
机构
[1] Univ Utrecht, Inst Biomembranes, Microbiol & Kluyver Ctr Genom Ind Fermentat, NL-3584 CH Utrecht, Netherlands
关键词
DOMINANT SELECTABLE MARKER; STRAND-BREAK REPAIR; CRYPTOCOCCUS-NEOFORMANS; HIGHLY-EFFICIENT; RESISTANCE GENE; EXPRESSION; BLEOMYCIN; BINDING; PROTEIN; DNA;
D O I
10.1128/AEM.02162-08
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Phleomycin is mutagenic by introducing double-strand breaks in DNA. The ble gene of Streptoalloteychus hindustanus, which confers resistance to this substance, is widely used as a selection marker for transformation. Schizophyllum commune grows on 25 mu g of phleomycin ml(-1) after introduction of a resistance cassette based on the ble gene. However, we here report that growth of resistant colonies on this concentration of phleomycin resulted in aberrant colony morphologies. Apparently, phleomycin was mutagenic despite acquired resistance. Therefore, a new selection system was developed based on resistance to the antibiotic nourseothricin. However, the transformation efficiency was tenfold lower than that obtained with phleomycin as a selection agent. This low transformation efficiency could be rescued by addition of a nonselective concentration of phleomycin during protoplast regeneration. This was accompanied by a higher incidence of single-copy integrations and with an increase of expression of key genes involved in double-strand break repair. Taken together, we conclude that the effect of a nonselective concentration of phleomycin strongly resembles the effect of restriction enzyme-mediated integration (REMI) but, unlike REMI, it does not depend on the presence of a target restriction site.
引用
收藏
页码:1243 / 1247
页数:5
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