CutA divalent cation tolerance homolog (Escherichia coli) (CUTA) regulates 尾-cleavage of 尾-amyloid precursor protein (APP) through interacting with 尾-site APP cleaving protein 1 (BACE1)

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	CutA divalent cation tolerance homolog (Escherichia coli) (CUTA) regulates 尾-cleavage of 尾-amyloid precursor protein (APP) through interacting with 尾-site APP cleaving protein 1 (BACE1)
	Zhao, Yingjun ; Wang, Yunshu ; Hu, Jin ; Zhang, Xian ; Zhang, Yun-Wu ; 张弦 ; 张云武
刊名	http://dx.doi.org/10.1074/jbc.M111.330209
	2012-03-30
关键词	Activation analysis Cell membranes Escherichia coli Interference suppression Mammals Neurodegenerative diseases Physiology Positive ions RNA
英文摘要	Accumulation of the neurotoxic 尾-amyloid (A尾) peptide in the brain is central to the pathogenesis of Alzheimer disease. A尾 is derived from the 尾-amyloid precursor protein (APP) through sequential cleavages by 尾- and 尾-secretases, and the production of A尾 is greatly affected by the subcellular localization of these factors. CUTA, the mammalian CutA divalent cation tolerance homolog (E. coli), has been proposed to mediate acetylcholinesterase activity and copper homeostasis, which are important in Alzheimer disease pathology. However, the exact function of CUTA remains largely unclear. Here we show that human CUTA has several variants that differ in their N-terminal length and are separated as heavy (H) and light (L) components. The H component has the longest N terminus and is membrane-associated, whereas the L component is N-terminally truncated at various sites and localized in the cytosol. Importantly, we demonstrate that the H component of CUTA interacts through its N terminus with the transmembrane domain of 尾-site APP cleaving enzyme 1 (BACE1), the putative 尾-secretase, mainly in the Golgi/trans-Golgi network. Overexpression and RNA interference knockdown of CUTA can reduce and increase BACE1-mediated APP processing/A尾 secretion, respectively. RNA interference of CUTA decelerates intracellular trafficking of BACE1 from the Golgi/trans-Golgi network to the cell surface and reduces the steady-state level of cell surface BACE1. Our results identify the H component of CUTA as a novel BACE1-interacting protein that mediates the intracellular trafficking of BACE1 and the processing of APP to A尾. 漏 2012 by The American Society for Biochemistry and Molecular Biology, Inc.
语种	英语
出版者	American Society for Biochemistry and Molecular Biology Inc.
内容类型	期刊论文
源URL	[http://dspace.xmu.edu.cn/handle/2288/93720]
专题	医学院－已发表论文
推荐引用方式 GB/T 7714	Zhao, Yingjun,Wang, Yunshu,Hu, Jin,等. CutA divalent cation tolerance homolog (Escherichia coli) (CUTA) regulates 尾-cleavage of 尾-amyloid precursor protein (APP) through interacting with 尾-site APP cleaving protein 1 (BACE1)[J]. http://dx.doi.org/10.1074/jbc.M111.330209,2012.
APA	Zhao, Yingjun.,Wang, Yunshu.,Hu, Jin.,Zhang, Xian.,Zhang, Yun-Wu.,...&张云武.(2012).CutA divalent cation tolerance homolog (Escherichia coli) (CUTA) regulates 尾-cleavage of 尾-amyloid precursor protein (APP) through interacting with 尾-site APP cleaving protein 1 (BACE1).http://dx.doi.org/10.1074/jbc.M111.330209.
MLA	Zhao, Yingjun,et al."CutA divalent cation tolerance homolog (Escherichia coli) (CUTA) regulates 尾-cleavage of 尾-amyloid precursor protein (APP) through interacting with 尾-site APP cleaving protein 1 (BACE1)".http://dx.doi.org/10.1074/jbc.M111.330209 (2012).