Vastiau I M K, Anthonio E A, Brams M, Brees C, Young S G, Van de Velde S, Wanders R J A, Mannaerts G P, Baes M, Van Veldhoven P P, Fransen M
Laboratorium voor Farmacologie, Departement Moleculaire Celbiologie, Faculteit Geneeskunde, Katholieke Universiteit Leuven, Campus Gasthuisberg (O/N 1), Herestraat 49 bus 601, 3000, Leuven, Belgium.
Cell Mol Life Sci. 2006 Jul;63(14):1686-99. doi: 10.1007/s00018-006-6110-y.
Pex19p exhibits a broad binding specificity for peroxisomal membrane proteins (PMPs), and is essential for the formation of functional peroxisomal membranes. Pex19p orthologues contain a C-terminal CAAX motif common to prenylated proteins. In addition, Saccharomyces cerevisiae and Chinese hamster Pex19p are at least partially farnesylated in vivo. Whether farnesylation of Pex19p plays an essential or merely ancillary role in peroxisome biogenesis is currently not clear. Here, we show that (i) nonfarnesylated and farnesylated human Pex19p display a similar affinity towards a select set of PMPs, (ii) a variant of Pex19p lacking a functional farnesylation motif is able to restore peroxisome biogenesis in Pex19p-deficient cells, and (iii) peroxisome protein import is not affected in yeast and mammalian cells defective in one of the enzymes involved in the farnesylation pathway. Summarized, these observations indicate that the CAAX box-mediated processing steps of Pex19p are dispensable for peroxisome biogenesis in yeast and mammalian cells.
Pex19p对过氧化物酶体膜蛋白(PMPs)具有广泛的结合特异性,并且对于功能性过氧化物酶体膜的形成至关重要。Pex19p直系同源物含有异戊二烯化蛋白共有的C末端CAAX基序。此外,酿酒酵母和中国仓鼠的Pex19p在体内至少部分被法尼基化。目前尚不清楚Pex19p的法尼基化在过氧化物酶体生物发生中是起关键作用还是仅仅起辅助作用。在这里,我们表明:(i)未被法尼基化和被法尼基化的人Pex19p对一组选定的PMPs表现出相似的亲和力;(ii)缺乏功能性法尼基化基序的Pex19p变体能够在Pex19p缺陷细胞中恢复过氧化物酶体生物发生;(iii)在法尼基化途径中涉及的一种酶有缺陷的酵母和哺乳动物细胞中,过氧化物酶体蛋白导入不受影响。总之,这些观察结果表明,Pex19p的CAAX盒介导的加工步骤对于酵母和哺乳动物细胞中的过氧化物酶体生物发生是可有可无的。