دورية أكاديمية

A novel FADS1 isoform potentiates FADS2-mediated production of eicosanoid precursor fatty acids.

التفاصيل البيبلوغرافية
العنوان: A novel FADS1 isoform potentiates FADS2-mediated production of eicosanoid precursor fatty acids.
المؤلفون: Park WJ; Division of Nutritional Sciences, Cornell University, Ithaca, NY., Kothapalli KS, Reardon HT, Lawrence P, Qian SB, Brenna JT
المصدر: Journal of lipid research [J Lipid Res] 2012 Aug; Vol. 53 (8), pp. 1502-12. Date of Electronic Publication: 2012 May 22.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 0376606 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1539-7262 (Electronic) Linking ISSN: 00222275 NLM ISO Abbreviation: J Lipid Res Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : [New York] : Elsevier
Original Publication: Memphis, Lipid Research, inc.
مواضيع طبية MeSH: Eicosanoids/*biosynthesis , Fatty Acid Desaturases/*genetics , Fatty Acid Desaturases/*metabolism, Alternative Splicing ; Animals ; Animals, Newborn ; Cell Differentiation ; Cell Line, Tumor ; Computational Biology ; Delta-5 Fatty Acid Desaturase ; Embryo, Mammalian/cytology ; Exons/genetics ; Gene Expression Regulation, Enzymologic ; Humans ; Intracellular Space/metabolism ; Isoenzymes/genetics ; Isoenzymes/metabolism ; Papio ; Poly A/genetics ; Poly A/metabolism ; Protein Transport ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Transcription, Genetic
مستخلص: The fatty acid desaturase (FADS) genes code for the rate-limiting enzymes required for the biosynthesis of long-chain polyunsaturated fatty acids (LCPUFA). Here we report discovery and function of a novel FADS1 splice variant. FADS1 alternative transcript 1 (FADS1AT1) enhances desaturation of FADS2, leading to increased production of eicosanoid precursors, the first case of an isoform modulating the enzymatic activity encoded by another gene. Multiple protein isoforms were detected in primate liver, thymus, and brain. In human neuronal cells, their expression patterns are modulated by differentiation and result in alteration of cellular fatty acids. FADS1, but not FADS1AT1, localizes to endoplasmic reticulum and mitochondria. Ribosomal footprinting demonstrates that all three FADS genes are translated at similar levels. The noncatalytic regulation of FADS2 desaturation by FADS1AT1 is a novel, plausible mechanism by which several phylogenetically conserved FADS isoforms may regulate LCPUFA biosynthesis in a manner specific to tissue, organelle, and developmental stage.
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معلومات مُعتمدة: T32 HD052471 United States HD NICHD NIH HHS; T32-HD-052471 United States HD NICHD NIH HHS
المشرفين على المادة: 0 (Delta-5 Fatty Acid Desaturase)
0 (Eicosanoids)
0 (Isoenzymes)
0 (RNA, Messenger)
24937-83-5 (Poly A)
EC 1.14.19.- (Fatty Acid Desaturases)
EC 1.14.19.3 (FADS1 protein, human)
EC 1.14.19.3 (FADS2 protein, human)
تواريخ الأحداث: Date Created: 20120524 Date Completed: 20121123 Latest Revision: 20211203
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC3540860
DOI: 10.1194/jlr.M025312
PMID: 22619218
قاعدة البيانات: MEDLINE
الوصف
تدمد:1539-7262
DOI:10.1194/jlr.M025312