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PEX11独立于过氧化物酶体代谢促进过氧化物酶体分裂。

PEX11 promotes peroxisome division independently of peroxisome metabolism.

作者信息

Li Xiaoling, Gould Stephen J

机构信息

Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

J Cell Biol. 2002 Feb 18;156(4):643-51. doi: 10.1083/jcb.200112028. Epub 2002 Feb 11.

Abstract

The PEX11 peroxisomal membrane proteins are the only factors known to promote peroxisome division in multiple species. It has been proposed that PEX11 proteins have a direct role in peroxisomal fatty acid oxidation, and that they only affect peroxisome abundance indirectly. Here we show that PEX11 proteins are unique in their ability to promote peroxisome division, and that PEX11 overexpression promotes peroxisome division in the absence of peroxisomal metabolic activity. We also observed that mouse cells lacking PEX11beta display reduced peroxisome abundance, even in the absence of peroxisomal metabolic substrates, and that PEX11beta(-/-) mice are partially deficient in two distinct peroxisomal metabolic pathways, ether lipid synthesis and very long chain fatty acid oxidation. Based on these and other observations, we propose that PEX11 proteins act directly in peroxisome division, and that their loss has indirect effects on peroxisome metabolism.

摘要

PEX11过氧化物酶体膜蛋白是已知的在多个物种中促进过氧化物酶体分裂的唯一因子。有人提出,PEX11蛋白在过氧化物酶体脂肪酸氧化中具有直接作用,并且它们仅间接影响过氧化物酶体丰度。在此我们表明,PEX11蛋白在促进过氧化物酶体分裂的能力方面是独特的,并且在缺乏过氧化物酶体代谢活性的情况下,PEX11的过表达促进过氧化物酶体分裂。我们还观察到,即使在没有过氧化物酶体代谢底物的情况下,缺乏PEX11β的小鼠细胞也表现出过氧化物酶体丰度降低,并且PEX11β(-/-)小鼠在两种不同的过氧化物酶体代谢途径,即醚脂合成和极长链脂肪酸氧化方面存在部分缺陷。基于这些及其他观察结果,我们提出PEX11蛋白直接参与过氧化物酶体分裂,并且它们的缺失对过氧化物酶体代谢有间接影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff2f/2174077/ef02c553bf5d/0112028f1.jpg

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