Oh Soon-Hwan, Cheng Georgina, Nuessen Jennifer A, Jajko Robert, Yeater Kathleen M, Zhao Xiaomin, Pujol Claude, Soll David R, Hoyer Lois L
Department of Veterinary Pathobiology, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA.
Department of Biological Sciences, The University of Iowa, Iowa City, IA 52242, USA.
Microbiology (Reading). 2005 Mar;151(Pt 3):673-681. doi: 10.1099/mic.0.27680-0.
Candida albicans strain SC5314 contains two ALS3 alleles, which differ in sequence with respect to the number of copies of the 108 bp tandem repeat sequence within the central domain of the coding region. One allele (ALS3(12)) has 12 tandem repeat copies while the other (ALS3(9)) has 9 copies. Wild-type C. albicans (ALS3(12)/ALS3(9)) and those containing various ALS3 alleles (ALS3(12)/als3Delta(9), als3Delta(12)/ALS3(9) and als3Delta(12)/als3Delta(9)) were assayed for adhesion to monolayers of cultured vascular endothelial and pharyngeal epithelial cells. These assays showed obvious adhesive function for the larger Als3p protein, compared to a minor contribution to adhesion from the smaller protein. These functional differences in strain SC5314 prompted examination of ALS3 allelic diversity across the five major genetic clades of C. albicans. This analysis focused on the number of copies of the tandem repeat sequence within the central domain of the coding region and showed a range of alleles encoding from 6 to 19 tandem repeat copies. Clades differed with respect to prevalent ALS3 alleles and allele distribution, but were similar for the mean number of tandem repeat copies per ALS3 allele. Analysis of allelic pairing showed clade differences and the tendency for C. albicans strains to encode one longer and one shorter ALS3 allele. The allelic variability observed for ALS3 and its functional consequences observed in strain SC5314 highlight the importance of understanding ALS allelic diversity in order to draw accurate conclusions about Als protein function.
白色念珠菌菌株SC5314含有两个ALS3等位基因,它们在编码区中央结构域内108 bp串联重复序列的拷贝数方面存在序列差异。一个等位基因(ALS3(12))有12个串联重复拷贝,而另一个(ALS3(9))有9个拷贝。对野生型白色念珠菌(ALS3(12)/ALS3(9))以及含有各种ALS3等位基因的菌株(ALS3(12)/als3Delta(9)、als3Delta(12)/ALS3(9)和als3Delta(12)/als3Delta(9))进行了与培养的血管内皮细胞和咽部上皮细胞单层的黏附检测。这些检测表明,较大的Als3p蛋白具有明显的黏附功能,相比之下较小的蛋白对黏附的贡献较小。菌株SC5314中的这些功能差异促使人们对白色念珠菌五个主要遗传分支中的ALS3等位基因多样性进行研究。该分析聚焦于编码区中央结构域内串联重复序列的拷贝数,结果显示一系列等位基因编码的串联重复拷贝数从6到19个不等。不同分支在常见的ALS3等位基因和等位基因分布方面存在差异,但每个ALS3等位基因的串联重复拷贝平均数相似。等位基因配对分析显示了分支差异以及白色念珠菌菌株编码一个较长和一个较短ALS3等位基因的趋势。在ALS3中观察到的等位基因变异性及其在菌株SC5314中观察到的功能后果凸显了了解ALS等位基因多样性对于准确推断Als蛋白功能的重要性。