Transcript variants of long-chain acyl-CoA synthase 1 have distinct roles in sheep lipid metabolism.
ACSL1
APA
lipid metabolism
sheep
transcript variants
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2022
2022
Historique:
received:
17
08
2022
accepted:
16
09
2022
entrez:
9
12
2022
pubmed:
10
12
2022
medline:
10
12
2022
Statut:
epublish
Résumé
Mutton has recently been identified to be a consumer favorite, and intermuscular fat is the key factor in determining meat tenderness. Long-chain acyl-CoA synthetase 1 (ACSL1) is a vital subtype of the ACSL family that is involved in the synthesis of lipids from acyl-CoA and the oxidation of fatty acids. The amplification of the ACSL1 gene using rapid amplification of cDNA ends revealed that the alternative polyadenylation (APA) results in two transcripts of the ACSL1 gene. Exon 18 had premature termination, resulting in a shorter CDS region. In this study, the existence of two transcripts of varying lengths translated normally and designated ACSL1-a and ACSL1-b was confirmed. Overexpression of ACSL1-a can promote the synthesis of an intracellular diglyceride, while ACSL1-b can promote triglyceride synthesis. The transfection of ACSL1 shRNA knocks down both the transcripts, the triglyceride content was significantly reduced after differentiation and induction; and lipidome sequencing results exhibited a significant decrease in 14-22 carbon triglyceride metabolites. The results of the present study indicated that the ACSL1 gene played a crucial role in the synthesis of triglycerides. Furthermore, the two transcripts involved in various interactions in the triglyceride synthesis process may be the topic of interest for future research and provide a more theoretical basis for sheep breeding.
Identifiants
pubmed: 36482895
doi: 10.3389/fgene.2022.1021103
pii: 1021103
pmc: PMC9723241
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1021103Informations de copyright
Copyright © 2022 Cao, Yu, Zhang, Liu, Zheng, Wang, Jin, Liu and Cao.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
J Biol Chem. 2004 Nov 5;279(45):46835-42
pubmed: 15337753
J Mol Cell Biol. 2012 Dec;4(6):352-61
pubmed: 23099521
J Biol Chem. 1990 May 25;265(15):8681-5
pubmed: 2341402
J Biol Chem. 1998 Feb 6;273(6):3132-5
pubmed: 9452420
Biochem Biophys Res Commun. 2012 Apr 13;420(3):588-93
pubmed: 22445754
Nucleic Acids Res. 2005 Jan 12;33(1):201-12
pubmed: 15647503
Cell Metab. 2010 Jul 7;12(1):53-64
pubmed: 20620995
Cell. 2009 Aug 21;138(4):673-84
pubmed: 19703394
Analyst. 2009 Oct;134(10):2003-11
pubmed: 19768207
Biochim Biophys Acta. 2014 Jun;1841(6):880-7
pubmed: 24631848
J Biol Chem. 2004 Jun 4;279(23):23882-91
pubmed: 15051725
Food Res Int. 2018 Feb;104:25-38
pubmed: 29433780
J Biol Chem. 2003 Apr 18;278(16):13860-6
pubmed: 12576479
Int J Mol Sci. 2020 Mar 17;21(6):
pubmed: 32192050
J Biol Chem. 1995 Apr 21;270(16):9676-82
pubmed: 7721900
PLoS One. 2016 Dec 19;11(12):e0168423
pubmed: 27992526
Asian-Australas J Anim Sci. 2017 Nov;30(11):1529-1539
pubmed: 28728367
J Biol Chem. 2001 Jul 6;276(27):24674-9
pubmed: 11319232
Nat Rev Gastroenterol Hepatol. 2017 Jun;14(6):343-355
pubmed: 28428634
J Biol Chem. 2002 Mar 8;277(10):8267-72
pubmed: 11751901
J Clin Invest. 2001 Apr;107(7):813-22
pubmed: 11285300
J Lipid Res. 1999 May;40(5):881-92
pubmed: 10224157
J Cell Sci. 2006 Nov 15;119(Pt 22):4678-88
pubmed: 17062637
Science. 2008 Jun 20;320(5883):1643-7
pubmed: 18566288