脂肪酸去饱和酶3 (FADS3)是反刍动物反式异戊酸特有的∆13-去饱和酶。

IF 2 4区 医学 Q3 GENETICS & HEREDITY
Lifestyle Genomics Pub Date : 2019-01-01 Epub Date: 2019-09-11 DOI:10.1159/000502356
Vincent Rioux, Philippe Legrand
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引用次数: 3

摘要

在哺乳动物物种中,脂肪酸去饱和酶(FADS)基因簇包括FADS1(∆5-去饱和酶)、FADS2(∆6-去饱和酶)和第三个基因成员FADS3。由于FADS3与fads1和FADS2的核苷酸序列高度同源,FADS3很快被该领域的研究人员怀疑编码了一种新的哺乳动物膜结合脂肪酸去饱和酶。然而,十年来一直没有发现FADS3蛋白具有催化活性,直到大鼠FADS3蛋白在体外被证明能够催化反式异戊酸出乎意料的∆13-去饱和,产生反式11、顺式13共轭亚油酸异构体。这篇综述总结了最近的研究,确定了FADS3酶是一种可靠的哺乳动物体内反式疫苗接种∆13-去饱和酶,并试图找出需要解决的进一步的未解决的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fatty Acid Desaturase 3 (FADS3) Is a Specific ∆13-Desaturase of Ruminant trans-Vaccenic Acid.

In mammalian species, the Fatty Acid Desaturase (FADS) gene cluster includes FADS1 (∆5-desaturase), FADS2 (∆6-desaturase), and a third gene member, named FADS3. According to its high degree of nucleotide sequence homology with both FADS1and FADS2, FADS3 was promptly suspected by researchers in the field to code for a new mammalian membrane-bound fatty acid desaturase. However, no catalytic activity was attributed to the FADS3 protein for a decade, until the rat FADS3 protein was shown in vitro to be able to catalyze the unexpected ∆13-desaturation of trans-vaccenic acid, producing the trans11,cis13-conjugated linoleic acid isomer. This review summarizes the recent investigations establishing the FADS3 enzyme as a reliable mammalian trans-vaccenate ∆13-desaturase in vivo and tries to identify further unresolved issues that need to be addressed.

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来源期刊
Lifestyle Genomics
Lifestyle Genomics Agricultural and Biological Sciences-Food Science
CiteScore
4.00
自引率
7.70%
发文量
11
审稿时长
28 weeks
期刊介绍: Lifestyle Genomics aims to provide a forum for highlighting new advances in the broad area of lifestyle-gene interactions and their influence on health and disease. The journal welcomes novel contributions that investigate how genetics may influence a person’s response to lifestyle factors, such as diet and nutrition, natural health products, physical activity, and sleep, amongst others. Additionally, contributions examining how lifestyle factors influence the expression/abundance of genes, proteins and metabolites in cell and animal models as well as in humans are also of interest. The journal will publish high-quality original research papers, brief research communications, reviews outlining timely advances in the field, and brief research methods pertaining to lifestyle genomics. It will also include a unique section under the heading “Market Place” presenting articles of companies active in the area of lifestyle genomics. Research articles will undergo rigorous scientific as well as statistical/bioinformatic review to ensure excellence.
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