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Molecular Mechanisms Underlying the Elevated Expression of a Potentially Type 2 Diabetes Mellitus Associated SCD1 Variant
Authors:Kinga Tibori,Gabriella Orosz,Veronika Zá  mbó  ,Pé  ter Szelé  nyi,Farkas Sarnyai,Viola Tamá  si,Zsolt Ró  nai,Judit Má  tyá  si,Blanka Tó  th,Mikló  s Csala,É  va Kereszturi
Affiliation:1.Department of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary; (K.T.); (G.O.); (V.Z.); (P.S.); (F.S.); (V.T.); (Z.R.);2.Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, H-1111 Budapest, Hungary; (J.M.); (B.T.)
Abstract:
Disturbances in lipid metabolism related to excessive food intake and sedentary lifestyle are among major risk of various metabolic disorders. Stearoyl-CoA desaturase-1 (SCD1) has an essential role in these diseases, as it catalyzes the synthesis of unsaturated fatty acids, both supplying for fat storage and contributing to cellular defense against saturated fatty acid toxicity. Recent studies show that increased activity or over-expression of SCD1 is one of the contributing factors for type 2 diabetes mellitus (T2DM). We aimed to investigate the impact of the common missense rs2234970 (M224L) polymorphism on SCD1 function in transfected cells. We found a higher expression of the minor Leu224 variant, which can be attributed to a combination of mRNA and protein stabilization. The latter was further enhanced by various fatty acids. The increased level of Leu224 variant resulted in an elevated unsaturated: saturated fatty acid ratio, due to higher oleate and palmitoleate contents. Accumulation of Leu224 variant was found in a T2DM patient group, however, the difference was statistically not significant. In conclusion, the minor variant of rs2234970 polymorphism might contribute to the development of obesity-related metabolic disorders, including T2DM, through an increased intracellular level of SCD1.
Keywords:stearoyl-CoA desaturase-1   single nucleotide polymorphism   fatty acids   type 2 diabetes mellitus   oleate   lipotoxicity   genetic variation   metabolic disorders   obesity
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