Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms21134736
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dc.titleMolecular cloning, characterization, and expression regulation of acyl-coa synthetase 6 gene and promoter in common carp cyprinus carpio
dc.contributor.authorXie, D.
dc.contributor.authorHe, Z.
dc.contributor.authorDong, Y.
dc.contributor.authorGong, Z.
dc.contributor.authorNie, G.
dc.contributor.authorLi, Y.
dc.date.accessioned2021-08-18T03:59:24Z
dc.date.available2021-08-18T03:59:24Z
dc.date.issued2020
dc.identifier.citationXie, D., He, Z., Dong, Y., Gong, Z., Nie, G., Li, Y. (2020). Molecular cloning, characterization, and expression regulation of acyl-coa synthetase 6 gene and promoter in common carp cyprinus carpio. International Journal of Molecular Sciences 21 (13) : 1-18. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms21134736
dc.identifier.issn16616596
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/197696
dc.description.abstractOmega-3 long chain polyunsaturated fatty acids (n-3 LC-PUFA), particularly docosahexaenoic acids (22:6n-3, DHA), have positive effects on multiple biologic and pathologic processes. Fish are the major dietary source of n-3 LC-PUFA for humans. Growing evidence supports acyl-coenzyme A (acyl-CoA) synthetase 6 (acsl6) being involved in cellular DHA uptake and lipogenesis in mammals, while its molecular function and regulatory mechanism remain unknown in fish. The present study focused on investigating the molecular characterization and transcription regulation of the acsl6 gene in the freshwater teleost common carp (Cyprinus carpio). First, the full length of acsl6 cDNA contained a coding region of 2148 bp for 715 amino acids, which possessed all characteristic features of the acyl-CoA synthetase (ACSL) family. Its mRNA expression was the highest in the brain, followed by in the heart, liver, kidney, muscle, and eyes, but little expression was detected in the ovary and gills. Additionally, a candidate acsl6 promoter region of 2058 bp was cloned, and the sequence from ?758 bp to ?198 bp was determined as core a promoter by equal progressive deletion and electrophoretic mobility shift assay. The binding sites for important transcription factors (TFs), including stimulatory protein 1 (SP1), CCAAT enhancer-binding protein (C/EBP?), sterol-regulatory element binding protein 1c (SREBP1c), peroxisome proliferator activated receptor ? (PPAR?), and PPAR? were identified in the core promoter by site-directed mutation and functional assays. Furthermore, the intraperitoneal injection of PPAR? agonists (balaglitazone) increased the expression of acsl6 mRNA, coupling with an increased proportion of DHA in the muscle, while opposite results were obtained in the injection of the SREBP1c antagonist (betulin). However, the expression of acsl6 and DHA content in muscle were largely unchanged by PPAR? agonist (fenofibrate) treatment. These results indicated that acsl6 may play an important role for the muscular DHA uptake and deposition in common carp, and PPAR? and SREBP-1c are the potential TFs involved in the transcriptional regulation of acsl6 gene. To our knowledge, this is the first report of the characterization of acsl6 gene and its promoter in teleosts. � 2020 by the authors. Licensee MDPI, Basel, Switzerland.
dc.publisherMDPI AG
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.subjectAcyl-CoA synthetase 6
dc.subjectCyprinus carpio
dc.subjectDHA deposition
dc.subjectTranscriptional regulation
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.3390/ijms21134736
dc.description.sourcetitleInternational Journal of Molecular Sciences
dc.description.volume21
dc.description.issue13
dc.description.page1-18
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