Kilaru Sreedhar, Collins Catherine M, Hartley Amanda J, Burns Claire, Foster Gary D, Bailey Andy M
School of Biological Sciences, University of Bristol, Woodland Road, Bristol, BS8 1UG, UK.
Curr Genet. 2009 Oct;55(5):543-50. doi: 10.1007/s00294-009-0266-6. Epub 2009 Jul 28.
Dominant selectable markers are beneficial for transformation of many fungi, particularly those model species where repeated transformations may be required. A carboxin resistance allele of the Coprinopsis cinerea sdi1 gene, encoding the iron-sulphur protein subunit of succinate dehydrogenase, was developed by introducing a suitable point mutation in the histidine block responsible for binding of the associated iron ion. This modified gene was used successfully to confer carboxin resistance upon transformation of C. cinerea protoplasts. Plasmids previously used to establish hygromycin transformation systems of several basidiomycete species, such as pAN7-1 and phph004, failed to give rise to hygromycin-resistant transformants of C. cinerea, whilst pPHT1 was successful. Sequencing of these constructs showed that the hygromycin resistance gene in pAN7-1 and phph004 had been modified removing the codons encoding two lysine residues following the N-terminal methionine. Replacement of the deleted 6 bp (AAA AAG) in the truncated hph gene led to generation of hygromycin-resistant transformants indicating the importance of these two codons for expression in C. cinerea. Phleomycin-resistant (ble) transformants were also obtained, but only with the intron-containing construct pblei004, showing that an intron is necessary to obtain phleomycin-resistant C. cinerea. This contrasts with hygromycin-resistance, where introns are not required for expression, emphasising the variability in importance of these elements.
显性选择标记有利于许多真菌的转化,特别是那些可能需要重复转化的模式物种。通过在负责结合相关铁离子的组氨酸区域引入合适的点突变,开发了灰盖鬼伞(Coprinopsis cinerea)sdi1基因的羧菌灵抗性等位基因,该基因编码琥珀酸脱氢酶的铁硫蛋白亚基。这个修饰后的基因成功用于在灰盖鬼伞原生质体转化时赋予羧菌灵抗性。以前用于建立几种担子菌物种潮霉素转化系统的质粒,如pAN7-1和phph004,未能产生灰盖鬼伞的潮霉素抗性转化体,而pPHT1则成功。对这些构建体的测序表明,pAN7-1和phph004中的潮霉素抗性基因已被修饰,去除了N端甲硫氨酸后编码两个赖氨酸残基的密码子。在截短的hph基因中替换缺失的6个碱基对(AAAAAG)导致产生潮霉素抗性转化体,表明这两个密码子对在灰盖鬼伞中的表达很重要。还获得了博来霉素抗性(ble)转化体,但仅使用含内含子的构建体pblei004,这表明内含子是获得博来霉素抗性灰盖鬼伞所必需的。这与潮霉素抗性形成对比,潮霉素抗性表达不需要内含子,强调了这些元件重要性的变异性。