Franz R, Michel S, Morschhäuser J
Zentrum für Infektionsforschung, Universität Würzburg, Röntgenring 11, D-97070, Würzburg, Germany.
Gene. 1998 Oct 5;220(1-2):91-8. doi: 10.1016/s0378-1119(98)00412-0.
Using primers derived from a region of the Candida albicans CDR1 (Candida drug resistance) gene that is conserved in other ABC (ATP-binding cassette) transporters, a DNA fragment from a previously unknown CDR gene was obtained by polymerase chain reaction (PCR). After screening a C. albicans genomic library with this fragment as a probe, the complete CDR4 gene was isolated and sequenced. CDR4 codes for a putative ABC transporter of 1490 amino acids with a high degree of homology to Cdr1p, Cdr2p and Cdr3p from C. albicans (62, 59 and 57% amino acid sequence identity, respectively). Cdr4p has a predicted structure typical for cluster I. 1 of yeast ABC transporters, characterized by two homologous halves, each comprising an N-terminal hydrophilic domain with consensus sequences for ATP binding and a C-terminal hydrophobic domain with six transmembrane helices. In contrast to the CDR1/CDR2 genes, the genetic structure of the CDR4 gene was conserved in 59 C. albicans isolates from six different patients. Northern hybridization analysis showed that the CDR4 gene was expressed in most isolates, but no correlation between CDR4 mRNA levels and the degree of fluconazole resistance of the isolates was found. In addition, a C. albicans mutant in which both copies of the CDR4 gene were disrupted by insertional mutagenesis was not hypersusceptible to fluconazole as compared to the parent strain. Unlike CDR1 and CDR2, CDR4 does not, therefore, seem to be involved in fluconazole resistance in C. albicans.
利用源自白色念珠菌CDR1(念珠菌耐药性)基因一个区域的引物,该区域在其他ABC(ATP结合盒)转运蛋白中保守,通过聚合酶链反应(PCR)获得了来自一个先前未知CDR基因的DNA片段。用该片段作为探针筛选白色念珠菌基因组文库后,分离并测序了完整的CDR4基因。CDR4编码一个推定的含1490个氨基酸的ABC转运蛋白,与白色念珠菌的Cdr1p、Cdr2p和Cdr3p具有高度同源性(氨基酸序列同一性分别为62%、59%和57%)。Cdr4p具有酵母ABC转运蛋白I.1簇典型的预测结构,其特征是由两个同源部分组成,每个部分包括一个具有ATP结合共有序列的N端亲水区和一个具有六个跨膜螺旋的C端疏水区。与CDR1/CDR2基因不同,CDR4基因的遗传结构在来自六名不同患者的59株白色念珠菌分离株中保守。Northern杂交分析表明,CDR4基因在大多数分离株中表达,但未发现CDR4 mRNA水平与分离株氟康唑耐药程度之间存在相关性。此外,与亲本菌株相比,通过插入诱变使CDR4基因的两个拷贝均被破坏的白色念珠菌突变体对氟康唑并不高度敏感。因此,与CDR1和CDR2不同,CDR4似乎不参与白色念珠菌对氟康唑的耐药性。