Costello Joseph L, Castro Inês G, Schrader Tina A, Islinger Markus, Schrader Michael
a Department of Biosciences , University of Exeter , Exeter , UK.
b Institute of Neuroanatomy, Center for Biomedicine & Medical Technology Mannheim, Medical Faculty Mannheim, University of Heidelberg , Mannheim , Germany.
Cell Cycle. 2017 Jun 3;16(11):1039-1045. doi: 10.1080/15384101.2017.1314422. Epub 2017 May 2.
Cooperation between cellular organelles such as mitochondria, peroxisomes and the ER is essential for a variety of important and diverse metabolic processes. Effective communication and metabolite exchange requires physical linkages between the organelles, predominantly in the form of organelle contact sites. At such contact sites organelle membranes are brought into close proximity by the action of molecular tethers, which often consist of specific protein pairs anchored in the membrane of the opposing organelles. Currently numerous tethering components have been identified which link the ER with multiple other organelles but knowledge of the factors linking the ER with peroxisomes is limited. Peroxisome-ER interplay is important because it is required for the biosynthesis of unsaturated fatty acids, ether-phospholipids and sterols with defects in these functions leading to severe diseases. Here, we characterize acyl-CoA binding domain protein 4 (ACBD4) as a tail-anchored peroxisomal membrane protein which interacts with the ER protein, vesicle-associated membrane protein-associated protein-B (VAPB) to promote peroxisome-ER associations.
线粒体、过氧化物酶体和内质网等细胞器之间的合作对于各种重要且多样的代谢过程至关重要。有效的通讯和代谢物交换需要细胞器之间的物理连接,主要形式为细胞器接触位点。在这些接触位点,细胞器膜通过分子系链的作用紧密靠近,分子系链通常由锚定在相对细胞器膜中的特定蛋白质对组成。目前已鉴定出许多将内质网与多种其他细胞器连接起来的系链成分,但关于将内质网与过氧化物酶体连接起来的因素的了解有限。过氧化物酶体-内质网相互作用很重要,因为它是不饱和脂肪酸、醚磷脂和固醇生物合成所必需的,这些功能的缺陷会导致严重疾病。在这里,我们将酰基辅酶A结合结构域蛋白4(ACBD4)鉴定为一种尾锚定的过氧化物酶体膜蛋白,它与内质网蛋白、囊泡相关膜蛋白相关蛋白B(VAPB)相互作用,以促进过氧化物酶体-内质网的结合。