Mesoderm-specific transcript is associated with fat mass expansion in response to a positive energy balance

被引:78
作者
Nikonova, Larissa [1 ]
Koza, Robert A. [1 ]
Mendoza, Tamra [1 ]
Chao, Pei-Min [1 ]
Curley, James P. [2 ]
Kozak, Leslie P. [1 ]
机构
[1] Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Univ Cambridge, Darwin Coll, Madingley, England
基金
美国国家卫生研究院;
关键词
nutritional programming; epigenetics; alpha/beta fold hydrolase; imprinted genes; obesity;
D O I
10.1096/fj.08-108266
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A 50-fold variation in mRNA and protein levels of the mesoderm-specific transcript gene (Mest) in white fat of C57BL/6J (B6) mice fed an obesogenic diet is positively correlated with expansion of fat mass. MEST protein was detected only in adipocytes, in which its induction occurred with both unsaturated and saturated dietary fat. To test the hypothesis that MEST modulates fat mass expansion, its expression was compared to that of stearoyl CoA desaturase (Scd1) in B6 mice exposed to diets and environmental temperatures that generated conditions separating the effects of food intake and adiposity. Under a range of conditions, Mest expression was always associated with variations in adiposity, whereas Scd1 expression was associated with the amount of saturated fat in the diet. Mest mRNA was expressed at its highest levels during early postnatal growth at the onset of the most rapid phase of fat mass expansion. MEST is localized to the endoplasmic reticulum/Golgi apparatus where its putative enzymatic properties as a lipase or acyltransferase, predicted from sequence homology with members of the alpha/beta fold hydrolase superfamily, can enable it to function in lipid accumulation under conditions of positive energy balance. Variations in adiposity and Mest expression in genetically identical mice also provides a model of epigenetic regulation. -Nikonova, L., Koza, R. A., Mendoza, T., Chao, P.-M., Curley, J. P., Kozak, L. P. Mesoderm-specific transcript is associated with fat mass expansion in response to a positive energy balance. FASEB J. 22, 3925-3937 (2008)
引用
收藏
页码:3925 / 3937
页数:13
相关论文
共 49 条
[1]   PLD1 and ERK2 regulate cytosolic lipid droplet formation [J].
Andersson, Linda ;
Bostrom, Pontus ;
Ericson, Johanna ;
Rutberg, Mikael ;
Magnusson, Bjorn ;
Marchesan, Denis ;
Ruiz, Michel ;
Asp, Lennart ;
Huang, Ping ;
Frohman, Michael A. ;
Boren, Jan ;
Olofsson, Sven-Olof .
JOURNAL OF CELL SCIENCE, 2006, 119 (11) :2246-2257
[2]   PPARγ is required for placental, cardiac, and adipose tissue development [J].
Barak, Y ;
Nelson, MC ;
Ong, ES ;
Jones, YZ ;
Ruiz-Lozano, P ;
Chien, KR ;
Koder, A ;
Evans, RM .
MOLECULAR CELL, 1999, 4 (04) :585-595
[3]   MILK-PRODUCTION AND CONSUMPTION AND GROWTH OF YOUNG OF WILD MICE AFTER 10 GENERATIONS IN A COLD ENVIRONMENT [J].
BARNETT, SA ;
DICKSON, RG .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 346 (JAN) :409-417
[4]   Regulation of Wnt signaling during adipogenesis [J].
Bennett, CN ;
Ross, SE ;
Longo, KA ;
Bajnok, L ;
Hemati, N ;
Johnson, KW ;
Harrison, SD ;
MacDougald, OA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (34) :30998-31004
[5]  
BLANCHETTEMACKIE EJ, 1995, J LIPID RES, V36, P1211
[6]   Cytosolic lipid droplets increase in size by microtubule-dependent complex formation [J].
Boström, P ;
Rutberg, M ;
Ericsson, J ;
Holmdahl, P ;
Andersson, L ;
Frohman, MA ;
Borén, J ;
Olofsson, SO .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (09) :1945-1951
[7]   Heterogeneous metabolic adaptation of C57BL/6J mice to high-fat diet [J].
Burcelin, M ;
Crivelli, V ;
Dacosta, A ;
Roy-Tirelli, A ;
Thorens, B .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 282 (04) :E834-E842
[8]   DISSECTING THE CATALYTIC TRIAD OF A SERINE PROTEASE [J].
CARTER, P ;
WELLS, JA .
NATURE, 1988, 332 (6164) :564-568
[9]   Bone morphogenetic protein-3 is a negative regulator of bone density [J].
Daluiski, A ;
Engstrand, T ;
Bahamonde, ME ;
Gamer, LW ;
Agius, E ;
Stevenson, SL ;
Cox, K ;
Rosen, V ;
Lyons, KM .
NATURE GENETICS, 2001, 27 (01) :84-88
[10]   Failure of adipocyte differentiation causes type II diabetes mellitus? [J].
Danforth, E .
NATURE GENETICS, 2000, 26 (01) :13-13