The genetic background modifies the effects of the obesity mutation, 'fatty', on apolipoprotein gene regulation in rat liver

被引:9
作者
Schuller, E
Patel, N
Item, C
Greber-Platzer, S
Baran, H
Patsch, W
Strobl, W
机构
[1] Univ Vienna, Sch Med, Dept Med Chem, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Pediat, Vienna, Austria
[3] Landeskrankenanstalten Salzburg, Dept Lab Med, Salzburg, Austria
关键词
obesity; leptin; apolipoproteins; genetics; diet;
D O I
10.1038/sj.ijo.0801179
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Obesity is associated with disorders of plasma lipid transport in many, but not in all obese subjects. The effects of obesity on the regulation of genes involved in plasma lipid transport may depend an specific mutations causing or contributing to obesity and/or on interactions of a specific obesity mutation with the genetic background. The 'fatty' (Glu269Pro) leptin receptor mutation causes severe obesity associated with hypertriglyceridaemia and altered hepatic apolipoprotein gene regulation in Zucker fatty rats. OBJECTIVE: To determine whether the effects of the obesity mutation 'fatty' on apolipoprotein gene regulation in rat liver depend on the genetic background. METHODS: We studied hepatic apolipoprotein (apo) A-IV, A-I, and C-lll gene expression in obese rats carrying the 'fatty' mutation on the background of the Zucker or Wistar strain. RESULTS: Basal apoA-IV gene expression was increased in fatty rats of both strains, whereas apoA-I and apoC-III gene expression differed between Wistar and Zucker fatty rats: apoA-I gene transcription was reduced to half and apoC-III mRNA was increased two-fold in Wistar fatty, but: not in Zucker fatty rats vs lean controls. A fish oil diet suppressed apoA-IV, but not apoA-I gene transcription in Wistar fatty rats, whereas in Zucker fatty rats apoA-IV transcription was unaffected, but apoA-I transcription was suppressed. CONCLUSIONS: Interactions of the 'fatty' leptin receptor mutation with the genetic background significantly affect the basal and diet-induced regulation of the apoA-IV, C-III and A-I genes in rat liver. The genetic background may therefore be a major determinant of the consequences of a specific obesity mutation for plasma lipid transport.
引用
收藏
页码:460 / 467
页数:8
相关论文
共 43 条
[1]   CORONARY HEART-DISEASE RISK-FACTORS IN MORBIDLY OBESE WOMEN WITH NORMAL GLUCOSE-TOLERANCE [J].
BARAKAT, HA ;
MOONEY, N ;
OBRIEN, K ;
LONG, S ;
KHAZANI, PG ;
PORIES, W ;
CARO, JF .
DIABETES CARE, 1993, 16 (01) :144-149
[2]   REGULATION OF RAT-LIVER APOLIPOPROTEIN-A-I, APOLIPOPROTEIN-A-II AND ACYL-COENZYME-A OXIDASE GENE-EXPRESSION BY FIBRATES AND DIETARY FATTY-ACIDS [J].
BERTHOU, L ;
SALADIN, R ;
YAQOOB, P ;
BRANELLEC, D ;
CALDER, P ;
FLUCHART, JC ;
DENEFLE, P ;
AUWERX, J ;
STAELS, B .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 232 (01) :179-187
[3]  
BIRCH HE, 1986, J BIOL CHEM, V261, P8077
[4]  
BOURGEOIS CS, 1995, AM J PHYSIOL, V296, pE208
[5]   The presence of the "fa" gene in heterozygous (FA/fn) lean female rats:: Effects on body weight, body fat and serum leptin [J].
Cleary, MP ;
Phillips, FC .
OBESITY RESEARCH, 1999, 7 (03) :293-298
[6]   THE INFLUENCE OF GENETIC BACKGROUND ON THE EXPRESSION OF MUTATIONS AT THE DIABETES (DB) LOCUS IN THE MOUSE .6. HEPATIC MALIC ENZYME-ACTIVITY IS ASSOCIATED WITH DIABETES SEVERITY [J].
COLEMAN, DL .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (10) :1134-1136
[7]   The search for human obesity genes [J].
Comuzzie, AG ;
Allison, DB .
SCIENCE, 1998, 280 (5368) :1374-1377
[8]   STRUCTURE AND EXPRESSION OF THE MOUSE BETA-2-MICROGLOBULIN GENE ISOLATED FROM SOMATIC AND NON-EXPRESSING TERATOCARCINOMA CELLS [J].
DANIEL, F ;
MORELLO, D ;
LEBAIL, O ;
CHAMBON, P ;
CAYRE, Y ;
KOURILSKY, P .
EMBO JOURNAL, 1983, 2 (07) :1061-1065
[9]   Protection against atherogenesis in mice mediated by human apolipoprotein A-IV [J].
Duverger, N ;
Tremp, G ;
Caillaud, JM ;
Emmanuel, F ;
Castro, G ;
Fruchart, JC ;
Steinmetz, A ;
Denefle, P .
SCIENCE, 1996, 273 (5277) :966-968
[10]   Chylomicronemia due to apolipoprotein CIII overexpression in apolipoprotein E-null mice - Apolipoprotein CIII-induced hypertriglyceridemia is not mediated by effects on apolipoprotein E [J].
Ebara, T ;
Ramakrishnan, R ;
Steiner, G ;
Shachter, NS .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (11) :2672-2681