Marshall J S, DeRocher A E, Keegstra K, Vierling E
Department of Botany, University of Wisconsin, Madison 53706.
Proc Natl Acad Sci U S A. 1990 Jan;87(1):374-8. doi: 10.1073/pnas.87.1.374.
Cytoplasmic members of the heat shock protein hsp70 family have recently been implicated in the transport of proteins to the endoplasmic reticulum and mitochondria. In addition, other hsp70 homologues have been found in the endoplasmic reticulum and mitochondria and, at least for the endoplasmic reticulum hsp70 homologue, may be involved in the proper folding and assembly of newly transported proteins. Since chloroplasts are an important site of protein transport in plant cells, we were interested in determining whether hsp70 proteins might be located in this organelle. By using immunoblotting techniques and two antibody preparations against hsp70 proteins, we have identified three chloroplastic proteins of approximately 70 kDa that are related to hsp70 proteins. One of these proteins was tightly associated with the outer envelope membrane and was not exposed at the outer surface of the chloroplasts. The other two were soluble proteins located in the stroma. Steady-state levels of the chloroplastic hsp70 homologues did not change after heat stress nor were any additional hsp70 homologues detected in chloroplasts isolated from heat-stressed plants. We discuss the possible functions of these hsp70 homologues in the transport of proteins into and within chloroplasts.
热休克蛋白hsp70家族的细胞质成员最近被认为与蛋白质向内质网和线粒体的转运有关。此外,在内质网和线粒体中还发现了其他hsp70同源物,至少对于内质网hsp70同源物来说,可能参与新转运蛋白质的正确折叠和组装。由于叶绿体是植物细胞中蛋白质转运的重要场所,我们有兴趣确定hsp70蛋白是否可能存在于这个细胞器中。通过使用免疫印迹技术和两种针对hsp70蛋白的抗体制剂,我们鉴定出了三种与hsp70蛋白相关的约70 kDa的叶绿体蛋白。其中一种蛋白与外膜紧密结合,未暴露在叶绿体的外表面。另外两种是位于基质中的可溶性蛋白。热胁迫后叶绿体hsp70同源物的稳态水平没有变化,在从热胁迫植物中分离出的叶绿体中也未检测到任何额外的hsp70同源物。我们讨论了这些hsp70同源物在蛋白质进入叶绿体和在叶绿体内转运中的可能功能。