Overlapping Roles of the Glucose-Responsive Genes, S14 and S14R, in Hepatic Lipogenesis

被引:31
作者
Aipoalani, Derrick L. [1 ]
O'Callaghan, Brennon L. [1 ]
Mashek, Douglas G. [2 ]
Mariash, Cary N. [3 ]
Towle, Howard C. [1 ]
机构
[1] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Food Sci & Nutr, Minneapolis, MN 55455 USA
[3] Methodist Res Inst, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
CENTER-DOT-MLX; THYROID-HORMONE; PRETRANSLATIONAL LEVEL; SPOT-14; PROTEIN; LIPID-SYNTHESIS; EXPRESSION; TRIIODOTHYRONINE; CARBOHYDRATE; HEPATOCYTE; CANCER;
D O I
10.1210/en.2009-1058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Spot 14 (S14; Thrsp) gene has been implicated in supporting regulated lipogenesis in mammals. S14 gene expression in liver is controlled by a wide variety of hormones and dietary factors in parallel with the major lipogenic enzyme genes. In addition, mice deleted for the S14 gene display reduced de novo lipogenesis in the lactating mammary gland. However, no decrease in hepatic lipogenesis was observed in the S14 null mouse. It was postulated that this difference could be due to the expression of a paralogous gene called S14R (S14 related; Mig12) in the liver but not mammary tissue. To test this hypothesis, we used small interfering RNA to simultaneously reduce levels of S14 and S14R in cultured primary hepatocytes. We found that rates of lipogenesis were decreased by approximately 65% in cells treated with insulin and high glucose. This reduction was associated with a decrease in total liver triacylglycerols and an altered morphology of lipid droplets. Expression of either S14 or S14R gene products was sufficient to fully restore normal lipogenesis. No change in the hepatic expression of other major lipogenic enzyme genes occurred during manipulation of S14 and/or S14R levels. These data support the hypothesis that both S14 and S14R are directly involved in supporting hepatic lipogenesis and that the two proteins play overlapping roles in this process. (Endocrinology 151: 2071-2077, 2010)
引用
收藏
页码:2071 / 2077
页数:7
相关论文
共 29 条
[1]   HIGH-YIELD PREPARATION OF ISOLATED RAT LIVER PARENCHYMAL CELLS - A BIOCHEMICAL AND FINE STRUCTURAL STUDY [J].
BERRY, MN ;
FRIEND, DS .
JOURNAL OF CELL BIOLOGY, 1969, 43 (03) :506-+
[2]   Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules [J].
Berti, C ;
Fontanella, B ;
Ferrentino, R ;
Meroni, G .
BMC CELL BIOLOGY, 2004, 5 (1)
[3]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[4]   ''Spot 14'' protein functions at the pretranslational level in the regulation of hepatic metabolism by thyroid hormone and glucose [J].
Brown, SB ;
Maloney, M ;
Kinlaw, WB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (04) :2163-2166
[5]   HIGH BASAL EXPRESSION AND 3,5,3'-TRIIODOTHYRONINE REGULATION OF MESSENGER RIBONUCLEIC-ACID S14 IN LIPOGENIC TISSUES [J].
JUMP, DB ;
OPPENHEIMER, JH .
ENDOCRINOLOGY, 1985, 117 (06) :2259-2266
[6]  
JUMP DB, 1984, J BIOL CHEM, V259, P2789
[7]   Functional interaction between sterol regulatory element-binding protein-1c, nuclear factor Y, and 3,5,3′-triiodothyronine nuclear receptors [J].
Jump, DB ;
Thelen, AP ;
Mater, MK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (37) :34419-34427
[8]   TRIIODOTHYRONINE RAPIDLY REVERSES INHIBITION OF S14 GENE-TRANSCRIPTION BY GLUCAGON [J].
KINLAW, WB ;
SCHWARTZ, HL ;
HAMBLIN, PS ;
MARIASH, CN ;
OPPENHEIMER, JH .
ENDOCRINOLOGY, 1988, 123 (05) :2255-2260
[9]   DIRECT EVIDENCE FOR A ROLE OF THE SPOT-14 PROTEIN IN THE REGULATION OF LIPID-SYNTHESIS [J].
KINLAW, WB ;
CHURCH, JL ;
HARMON, J ;
MARIASH, CN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (28) :16615-16618
[10]   Fatty acid synthase and cancer: New application of an old pathway [J].
Kuhajda, FP .
CANCER RESEARCH, 2006, 66 (12) :5977-5980