Maternal protein restriction with or without folic acid supplementation during pregnancy alters the hepatic transcriptome in adult male rats

被引:63
作者
Lillycrop, Karen A. [1 ]
Rodford, Joanne [2 ]
Garratt, Emma S. [2 ]
Slater-Jefferies, Joanne L. [2 ]
Godfrey, Keith M. [3 ]
Gluckman, Peter D. [4 ]
Hanson, Mark A. [2 ]
Burdge, Graham C. [2 ]
机构
[1] Univ Southampton, Southampton SO16 7PX, Hants, England
[2] Southampton Gen Hosp, Inst Dev Sci, Southampton SO16 6YD, Hants, England
[3] Southampton Gen Hosp, MRC, Epidemiol Resource Ctr, Southampton SO16 6YD, Hants, England
[4] Univ Auckland, Liggins Inst, Auckland 1, New Zealand
关键词
EPIGENETIC MODIFICATION; DIETARY-PROTEIN; GENE-EXPRESSION; IN-UTERO; GLUCOCORTICOID-RECEPTOR; EARLY-LIFE; METHYLATION; FAT; HYPERTENSION; EXPOSURE;
D O I
10.1017/S0007114509993795
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Feeding pregnant rats a protein-restricted (PR) diet induces altered expression of candidate genes in the liver of the adult offspring, which can be prevented by supplementation of the PR diet with folic acid (PRF). We investigated the effect of maternal nutrition during pregnancy on the liver transcriptome in their adult male offspring. Pregnant rats were fed control, PR or PRF diets. Male offspring were killed on day 84. The liver transcriptome was analysed by microarray (six livers per maternal dietary group) followed by post hoc analysis of relative mRNA levels and gene ontology. These results were confirmed for selected genes by real-time RT-PCR. There were 311 genes that differed significantly (>= 1.5-fold change; P<0.05) between PR offspring (222 increased) and control offspring, while 191 genes differed significantly between PRF offspring (forty-five increased) compared with offspring of control dams. There were sixteen genes that were significantly altered in both PR and PRF offspring compared with controls. Ion transport, developmental process, and response to reactive oxygen species (RROS) and steroid hormone response (SHR) ontologies were altered in PR offspring. Folic acid supplementation prevented changes within RROS and SHR response pathways, but not in ion transport or developmental process. There was no effect of maternal PR on mRNA expression of imprinted genes. Insulin 1 and Pleckstrin homology-like domain family A member 2 were increased significantly in PRF compared with PR offspring. The present findings show that the pattern of induced changes in the adult liver transcriptome were dependent on maternal protein and folic acid intakes during pregnancy.
引用
收藏
页码:1711 / 1719
页数:9
相关论文
共 46 条
[1]   A review of known imprinting syndromes and their association with assisted reproduction technologies [J].
Amor, David J. ;
Halliday, Jane .
HUMAN REPRODUCTION, 2008, 23 (12) :2826-2834
[2]   Experimental models of developmental programming: consequences of exposure to an energy rich diet during development [J].
Armitage, JA ;
Taylor, PD ;
Poston, L .
JOURNAL OF PHYSIOLOGY-LONDON, 2005, 565 (01) :3-8
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]   Developmental plasticity and human health [J].
Bateson, P ;
Barker, D ;
Clutton-Brock, T ;
Deb, D ;
D'Udine, B ;
Foley, RA ;
Gluckman, P ;
Godfrey, K ;
Kirkwood, T ;
Lahr, MM ;
McNamara, J ;
Metcalfe, NB ;
Monaghan, P ;
Spencer, HG ;
Sultan, SE .
NATURE, 2004, 430 (6998) :419-421
[5]   Prenatal exposure to a maternal low-protein diet programmes a preference for high-fat foods in the young adult rat [J].
Bellinger, L ;
Lilley, C ;
Langley-Evans, SC .
BRITISH JOURNAL OF NUTRITION, 2004, 92 (03) :513-520
[6]   Exposure to undernutrition in fetal life determines fat distribution, locomotor activity and food intake in ageing rats [J].
Bellinger, L ;
Sculley, DV ;
Langley-Evans, SC .
INTERNATIONAL JOURNAL OF OBESITY, 2006, 30 (05) :729-738
[7]   The maternal diet during pregnancy programs altered expression of the glucocorticoid receptor and type 2 11β-hydroxysteroid dehydrogenase:: Potential molecular mechanisms underlying the programming of hypertension in utero [J].
Bertram, C ;
Trowern, AR ;
Copin, N ;
Jackson, AA ;
Whorwood, CB .
ENDOCRINOLOGY, 2001, 142 (07) :2841-2853
[8]   Animal models and programming of the metabolic syndrome [J].
Bertram, CE ;
Hanson, MA .
BRITISH MEDICAL BULLETIN, 2001, 60 :103-121
[9]   Investigation of the role of epigenetic modification of the rat glucokinase gene in fetal programming [J].
Bogdarina, I ;
Murphy, HC ;
Burns, SP ;
Clark, AJL .
LIFE SCIENCES, 2004, 74 (11) :1407-1415
[10]   Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension [J].
Bogdarina, Irina ;
Welham, Simon ;
King, Peter J. ;
Burns, Shamus P. ;
Clark, Adrian J. L. .
CIRCULATION RESEARCH, 2007, 100 (04) :520-526