Barnes D, Lai W, Breslav M, Naider F, Becker J M
Department of Microbiology and University of Tennessee, Knoxville 37996-0845, USA.
Mol Microbiol. 1998 Jul;29(1):297-310. doi: 10.1046/j.1365-2958.1998.00931.x.
We have isolated and characterized the Saccharomyces cerevisiae PTR3 gene by functional complementation of a mutant deficient for amino acid-inducible peptide transport. PTR3 is predicted to encode a protein of 678 amino acids that exhibits no similarity to any other protein in the database. Deletion of the PTR3 open reading frame pleiotropically reduced the sensitivity to toxic peptides and amino acid analogues. Initial rates of radiolabelled dipeptide uptake demonstrated that elimination of PTR3 resulted in the loss of amino acid-induced levels of peptide transport. PTR3 was required for amino acid-induced expression of PTR2, the gene encoding the dipeptide/tripeptide transport protein, but was not necessary for nitrogen catabolite repression of peptide import or PTR2 expression. It was determined that PTR3 also modulates expression of BAP2, the gene encoding the branched-amino acid permease. Furthermore, we present genetic evidence that suggests that PTR3 functions within a novel regulatory pathway that facilitates amino acid induction of the PTR system.
我们通过对氨基酸诱导肽转运缺陷型突变体进行功能互补,分离并鉴定了酿酒酵母PTR3基因。PTR3预计编码一个由678个氨基酸组成的蛋白质,该蛋白质与数据库中的任何其他蛋白质均无相似性。PTR3开放阅读框的缺失多效性地降低了对有毒肽和氨基酸类似物的敏感性。放射性标记二肽摄取的初始速率表明,PTR3的缺失导致氨基酸诱导的肽转运水平丧失。PTR3是氨基酸诱导的PTR2表达所必需的,PTR2是编码二肽/三肽转运蛋白的基因,但对于肽导入的氮代谢物阻遏或PTR2表达并非必需。已确定PTR3还调节BAP2的表达,BAP2是编码支链氨基酸通透酶的基因。此外,我们提供的遗传学证据表明,PTR3在促进PTR系统氨基酸诱导的新型调控途径中发挥作用。