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Loss of Heterozygosity at an Unlinked Genomic Locus Is Responsible for the Phenotype of a Candida albicans sap4Δ sap5Δ sap6Δ Mutant

机译:在白色的念珠菌sap4Δsap5Δsap6Δ突变体的表型负责在一个未链接的基因组位点杂合性的损失。

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The diploid genome of the pathogenic yeast Candida albicans exhibits a high degree of heterozygosity. Genomic alterations that result in a loss of heterozygosity at specific loci may affect phenotypes and confer a selective advantage under certain conditions. Such genomic rearrangements can also occur during the construction of C. albicans mutants and remain undetected. The SAP2 gene on chromosome R encodes a secreted aspartic protease that is induced and required for growth of C. albicans when proteins are the only available nitrogen source. In strain SC5314, the two SAP2 alleles are functionally divergent because of differences in their regulation. Basal expression of the SAP2-2 allele, but not the SAP2-1 allele, provides the proteolytic degradation products that serve as inducers for full SAP2 induction. A triple mutant lacking the SAP4, SAP5, and SAP6 genes, which are located on chromosome 6, has previously been reported to have a growth defect on proteins, suggesting that one of the encoded proteases is required for SAP2 expression. Here we show that this sap4Δ sap5Δ sap6Δ mutant has become homozygous for chromosome R and lost the SAP2-2 allele. Replacement of one of the SAP2-1 copies in this strain by SAP2-2 and its regulatory region restored the ability of the sap4Δ sap5Δ sap6Δ mutant to utilize proteins as the sole nitrogen source. This is an illustrative example of how loss of heterozygosity at a different genomic locus can cause the mutant phenotype attributed to targeted deletion of a specific gene in C. albicans.
机译:致病性酵母白色念珠菌的二倍体基因组表现出高度的杂合性。在特定位点导致杂合性丧失的基因组改变可能会影响表型,并在某些条件下赋予选择性优势。这样的基因组重排也可以在白色念珠菌突变体的构建过程中发生并且未被发现。 R染色体上的 SAP2 基因编码一种分泌的天冬氨酸蛋白酶,当蛋白质是唯一可用的氮源时,该蛋白酶被诱导并为白色念珠菌的生长所必需。在SC5314菌株中,两个 SAP2 等位基因在功能上存在差异,因为它们的调控方式不同。 SAP2 - 2 等位基因的基础表达,而不是 SAP2 - 1 等位基因,提供蛋白水解降解产物可以完全诱导 SAP2 。缺少报道位于6号染色体上的缺少 SAP4 SAP5 SAP6 基因的三重突变体蛋白质上,提示 SAP2 表达需要一种编码的蛋白酶。在这里,我们显示此 sap4 Δ sap5 Δ sap6 Δ突变体已成为染色体R的纯合子,并丢失了 SAP2 - 2 等位基因。该菌株中的 SAP2 - 1 拷贝之一被 SAP2 - 2 取代,并且其调控区恢复了突变体 sap4 Δ sap5 Δ sap6 Δ利用蛋白质作为唯一氮源的能力。这是一个说明性的例子,说明在不同基因组位点的杂合性丧失如何导致突变表型归因于白色念珠菌中特定基因的靶向缺失。

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