Wang Xiaodong, McMahon Moira A, Shelton Shary N, Nampaisansuk Mongkol, Ballard Johnathan L, Goodman Joel M
Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9041, USA.
Mol Biol Cell. 2004 Apr;15(4):1702-10. doi: 10.1091/mbc.e03-11-0810. Epub 2004 Jan 23.
Several peroxisomal proteins have two nonoverlapping targeting signals. These signals have been termed "redundant" because targeting can still occur with only one signal. We now report that separate targeting motifs within both Pmp47 and Pex8 provide complementary function. Pmp47 is an ATP translocator that contains six transmembrane domains (TMDs). We had previously shown that the TMD2 region (termed TMD2R, consisting of TMD2 and a short adjacent segment of cytosolic loop) was required for targeting to proliferated peroxisomes in Saccharomyces cerevisiae. We now report that the analogous TMD4R, which cannot target to proliferated peroxisomes, targets at least as well, or much better (depending on strain and growth conditions) in cells containing only basal (i.e., nonproliferated) peroxisomes. These data suggest differences in the targeting pathway among peroxisome populations. Pex8p, a peripheral protein facing the matrix, contains a typical carboxy terminal targeting sequence (PTS1) that has been shown to be nonessential for targeting, indicating the existence of a second targeting domain (not yet defined in S. cerevisiae); thus, its function was unknown. We show that targeting to basal peroxisomes, but not to proliferated peroxisomes, is more efficient with the PTS1 than without it. Our results indicate that multiple targeting signals within peroxisomal proteins extend coverage among heterogeneous populations of peroxisomes and increase efficiency of targeting in some metabolic states.
几种过氧化物酶体蛋白具有两个不重叠的靶向信号。这些信号被称为“冗余”信号,因为仅一个信号时靶向仍可发生。我们现在报告,Pmp47和Pex8内的不同靶向基序具有互补功能。Pmp47是一种ATP转运体,含有六个跨膜结构域(TMD)。我们之前已经表明,TMD2区域(称为TMD2R,由TMD2和胞质环的一小段相邻片段组成)是酿酒酵母中靶向增殖过氧化物酶体所必需的。我们现在报告,类似的TMD4R不能靶向增殖过氧化物酶体,但在仅含有基础(即未增殖)过氧化物酶体的细胞中,其靶向效果至少一样好,或者更好(取决于菌株和生长条件)。这些数据表明过氧化物酶体群体之间靶向途径存在差异。Pex8p是一种面向基质的外周蛋白,含有一个典型的羧基末端靶向序列(PTS1),已证明该序列对靶向并非必需,这表明存在第二个靶向结构域(在酿酒酵母中尚未定义);因此,其功能未知。我们表明,对于基础过氧化物酶体的靶向,有PTS1时比没有PTS1时更有效,但对于增殖过氧化物酶体则不然。我们的结果表明,过氧化物酶体蛋白内的多个靶向信号扩大了在异质性过氧化物酶体群体中的覆盖范围,并在某些代谢状态下提高了靶向效率。