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在萤火虫荧光素酶羧基末端鉴定过氧化物酶体靶向信号。

Identification of a peroxisomal targeting signal at the carboxy terminus of firefly luciferase.

作者信息

Gould S G, Keller G A, Subramani S

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093.

出版信息

J Cell Biol. 1987 Dec;105(6 Pt 2):2923-31. doi: 10.1083/jcb.105.6.2923.

Abstract

Translocation of proteins across membranes of the endoplasmic reticulum, mitochondrion, and chloroplast has been shown to be mediated by targeting signals present in the transported proteins. To test whether the transport of proteins into peroxisomes is also mediated by a peptide targeting signal, we have studied the firefly luciferase gene that encodes a protein transported to peroxisomes in both insect and mammalian cells. We have identified two regions of luciferase which are necessary for transport of this protein into peroxisomes. We demonstrate that one of these, region II, represents a peroxisomal targeting signal because it is both necessary and sufficient for directing cytosolic proteins to peroxisomes. The signal is no more than twelve amino acids long and is located at the extreme carboxy-terminus of luciferase. The location of the targeting signal for translocation across the peroxisomal membrane therefore differs from the predominantly amino-terminal location of signals responsible for transport across the membranes of the endoplasmic reticulum, chloroplast, or mitochondrion.

摘要

蛋白质跨内质网、线粒体和叶绿体膜的转运已被证明是由被转运蛋白质中存在的靶向信号介导的。为了测试蛋白质进入过氧化物酶体的转运是否也由肽靶向信号介导,我们研究了萤火虫荧光素酶基因,该基因编码一种在昆虫和哺乳动物细胞中都被转运到过氧化物酶体的蛋白质。我们已经确定了荧光素酶的两个区域,它们是该蛋白质进入过氧化物酶体所必需的。我们证明其中一个区域,即区域II,代表过氧化物酶体靶向信号,因为它对于将胞质蛋白导向过氧化物酶体既是必需的也是充分的。该信号长度不超过十二个氨基酸,位于荧光素酶的极端羧基末端。因此,跨过氧化物酶体膜转运的靶向信号的位置与负责跨内质网、叶绿体或线粒体膜转运的信号主要位于氨基末端的位置不同。

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