Epigenetic regulation and fetal programming
Tóm tắt
Từ khóa
Tài liệu tham khảo
McMillen, 2005, Developmental origins of the metabolic syndrome: prediction, plasticity, and programming, Physiological Reviews, 85, 571, 10.1152/physrev.00053.2003
Gluckman, 2007, Early life events and their consequences for later disease: a life history and evolutionary perspective, American Journal of Human Biology, 19, 1, 10.1002/ajhb.20590
Neel, 1962, Diabetes mellitus: a ‘thrifty’ genotype rendered detrimental by ‘progress’?, American Journal of Human Genetics, 14, 353
Hales, 1992, Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis, Diabetologia, 35, 595, 10.1007/BF00400248
Barker, 1993, Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth, Diabetologia, 36, 62, 10.1007/BF00399095
Gluckman, 2004, Living with the past: evolution, development, and patterns of disease, Science, 305, 1733, 10.1126/science.1095292
Gluckman, 2005, Environmental influences during development and their later consequences for health and disease: implications for the interpretation of empirical studies, Proceedings. Biological Sciences, 272, 671, 10.1098/rspb.2004.3001
Gluckman, 2007, Developmental plasticity and human disease: research directions, Journal of Internal Medicine, 261, 461, 10.1111/j.1365-2796.2007.01802.x
Fowden, 2006, Intrauterine programming of physiological systems: causes and consequences, Physiology (Bethesda, Md.), 21, 29, 10.1152/physiol.00050.2005
Roseboom, 2006, The Dutch famine and its long-term consequences for adult health, Early Human Development, 82, 485, 10.1016/j.earlhumdev.2006.07.001
Fowden, 2005, Endocrine and metabolic programming during intrauterine development, Early Human Development, 81, 723, 10.1016/j.earlhumdev.2005.06.007
Karlberg, 1997, The timing of early postnatal catch-up growth in normal, full-term infants born short for gestational age, Hormone Research, 48, 17, 10.1159/000191279
Ong, 2000, Association between postnatal catch-up growth and obesity in childhood: prospective cohort study, BMJ (Clinical Research Ed.), 320, 967, 10.1136/bmj.320.7240.967
Jaquet, 2000, Insulin resistance early in adulthood in subjects born with intrauterine growth retardation, The Journal of Clinical Endocrinology and Metabolism, 85, 1401, 10.1210/jc.85.4.1401
Huxley, 2000, The role of size at birth and postnatal catch-up growth in determining systolic blood pressure: a systematic review of the literature, Journal of Hypertension, 18, 815, 10.1097/00004872-200018070-00002
Seckl, 2004, Prenatal glucocorticoids and long-term programming, European Journal of Endocrinology/European Federation of Endocrine Societies, 151, U49, 10.1530/eje.0.151U049
Matthews, 2002, Early programming of the hypothalamo-pituitary-adrenal axis, Trends in Endocrinology and Metabolism, 13, 373, 10.1016/S1043-2760(02)00690-2
Lesage, 2001, Maternal undernutrition during late gestation induces fetal overexposure to glucocorticoids and intrauterine growth retardation, and disturbs the hypothalamo-pituitary adrenal axis in the newborn rat, Endocrinology, 142, 1692, 10.1210/en.142.5.1692
Fowden, 2001, Intra-uterine programming of the endocrine pancreas, British Medical Bulletin, 60, 123, 10.1093/bmb/60.1.123
Petrik, 1998, Apoptosis in the pancreatic islet cells of the neonatal rat is associated with a reduced expression of insulin-like growth factor II that may act as a survival factor, Endocrinology, 139, 2994, 10.1210/en.139.6.2994
Boujendar, 2002, Taurine supplementation to a low protein diet during fetal and early postnatal life restores a normal proliferation and apoptosis of rat pancreatic islets, Diabetologia, 45, 856, 10.1007/s00125-002-0833-6
Ozanne, 2002, Early programming of glucose-insulin metabolism, Trends in Endocrinology and Metabolism, 13, 368, 10.1016/S1043-2760(02)00666-5
Heude, 2007, Study of association between common variation in the IGF2 gene and indices of obesity and body size in middle-age men and women, The Journal of Clinical Endocrinology and Metabolism, 92, 2734, 10.1210/jc.2006-1948
Murrell, 2004, An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype, Human Molecular Genetics, 13, 247, 10.1093/hmg/ddh013
Petry, 2005, Genetic variation in the type 2 insulin-like growth factor receptor gene and disparity in childhood height, Growth Hormone & IGF Research, 15, 363, 10.1016/j.ghir.2005.07.003
Gaunt, 2001, Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males, Human Molecular Genetics, 10, 1491, 10.1093/hmg/10.14.1491
Roth, 2002, IGF2 genotype and obesity in men and women across the adult age span, International Journal of Obesity and Related Metabolic Disorders, 26, 585, 10.1038/sj.ijo.0801927
Petry, 2005, Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans, BMC Genetics, 6, 22, 10.1186/1471-2156-6-22
Fowden, 2003, The insulin-like growth factors and feto-placental growth, Placenta, 24, 803, 10.1016/S0143-4004(03)00080-8
Arends, 2002, Polymorphism in the IGF-I gene: clinical relevance for short children born small for gestational age (SGA), The Journal of Clinical Endocrinology and Metabolism, 87, 2720, 10.1210/jc.87.6.2720
Vaessen, 2002, Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight, Lancet, 359, 1036, 10.1016/S0140-6736(02)08067-4
Johnston, 2003, Association between insulin-like growth factor I (IGF-I) polymorphisms, circulating IGF-I, and pre- and postnatal growth in two European small for gestational age populations, The Journal of Clinical Endocrinology and Metabolism, 88, 4805, 10.1210/jc.2003-030563
Frayling, 2002, A putative functional polymorphism in the IGF-I gene: association studies with type 2 diabetes, adult height, glucose tolerance, and fetal growth in U.K. populations, Diabetes, 51, 2313, 10.2337/diabetes.51.7.2313
Hattersley, 1999, The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease, Lancet, 353, 1789, 10.1016/S0140-6736(98)07546-1
Frayling, 2001, The role of genetic susceptibility in the association of low birth weight with type 2 diabetes, British Medical Bulletin, 60, 89, 10.1093/bmb/60.1.89
Hattersley, 1998, Mutations in the glucokinase gene of the fetus result in reduced birth weight, Nature Genetics, 19, 268, 10.1038/953
Eriksson, 2002, The effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-gamma2 gene on insulin sensitivity and insulin metabolism interact with size at birth, Diabetes, 51, 2321, 10.2337/diabetes.51.7.2321
Dunger, 2006, Genetic variations and normal fetal growth, Hormone Research, 65, 34, 10.1159/000091504
Le Stunff, 2000, The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesity, Nature Genetics, 26, 444, 10.1038/82579
Le Fur, 2006, Heterogeneity of class I INS VNTR allele association with insulin secretion in obese children, Physiological Genomics, 25, 480, 10.1152/physiolgenomics.00311.2005
Le Stunff, 2001, Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity, Nature Genetics, 29, 96, 10.1038/ng707
Waterland, 2004, Early nutrition, epigenetic changes at transposons and imprinted genes, and enhanced susceptibility to adult chronic diseases, Nutrition, 20, 63, 10.1016/j.nut.2003.09.011
Feil, 2006, Environmental and nutritional effects on the epigenetic regulation of genes, Mutation Research, 600, 46, 10.1016/j.mrfmmm.2006.05.029
Jaenisch, 2003, Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals, Nature Genetics, 33, 245, 10.1038/ng1089
Jirtle, 2007, Environmental epigenomics and disease susceptibility, Nature Reviews. Genetics, 8, 253, 10.1038/nrg2045
Godfrey, 2007, Epigenetic mechanisms and the mismatch concept of the developmental origins of health and disease, Pediatric Research, 61, 5R, 10.1203/pdr.0b013e318045bedb
Vickaryous, 2005, The role of early embryonic environment on epigenotype and phenotype, Reproduction, Fertility, and Development, 17, 335, 10.1071/RD04133
Egger, 2004, Epigenetics in human disease and prospects for epigenetic therapy, Nature, 429, 457, 10.1038/nature02625
Reik, 2001, Genomic imprinting: parental influence on the genome, Nature Reviews. Genetics, 2, 21, 10.1038/35047554
El-Osta, 2004, Understanding the consequences of epigenetic mechanisms and its effects on transcription in health and disease, Cancer Biology & Therapy, 3, 816, 10.4161/cbt.3.9.1100
Wassenegger, 2005, The role of the RNAi machinery in heterochromatin formation, Cell, 122, 13, 10.1016/j.cell.2005.06.034
Harikrishnan, 2005, Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing, Nature Genetics, 37, 254, 10.1038/ng1516
Delaval, 2004, Epigenetic regulation of mammalian genomic imprinting, Current Opinion in Genetics & Development, 14, 188, 10.1016/j.gde.2004.01.005
Constancia, 2002, Placental-specific IGF-II is a major modulator of placental and fetal growth, Nature, 417, 945, 10.1038/nature00819
Constancia, 2005, Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems, Proceedings of the National Academy of Sciences of the United States of America, 102, 19219, 10.1073/pnas.0504468103
Angiolini, 2006, Regulation of placental efficiency for nutrient transport by imprinted genes, Placenta, 27, S98, 10.1016/j.placenta.2005.12.008
Fowden, 2006, Programming placental nutrient transport capacity, The Journal of Physiology, 572, 5, 10.1113/jphysiol.2005.104141
Reik, 2001, Epigenetic reprogramming in mammalian development, Science, 293, 1089, 10.1126/science.1063443
Gicquel, 2005, Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver–Russell syndrome, Nature Genetics, 37, 1003, 10.1038/ng1629
Gaston, 2001, Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome, European Journal of Human Genetics, 9, 409, 10.1038/sj.ejhg.5200649
Poulsen, 2007, The epigenetic basis of twin discordance in age-related diseases, Pediatric Research, 61, 38R, 10.1203/pdr.0b013e31803c7b98
Fraga, 2005, Epigenetic differences arise during the lifetime of monozygotic twins, Proceedings of the National Academy of Sciences of the United States of America, 102, 10604, 10.1073/pnas.0500398102
Wong, 2005, Phenotypic differences in genetically identical organisms: the epigenetic perspective, Human Molecular Genetics, 14 Spec No 1, R11, 10.1093/hmg/ddi116
Kant, 2005, Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated region, Human Genetics, 117, 398, 10.1007/s00439-005-1304-1
Weksberg, 2002, Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome, Human Molecular Genetics, 11, 1317, 10.1093/hmg/11.11.1317
Khosla, 2001, Culture of preimplantation embryos and its long-term effects on gene expression and phenotype, Human Reproduction Update, 7, 419, 10.1093/humupd/7.4.419
Doherty, 2000, Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo, Biology of Reproduction, 62, 1526, 10.1095/biolreprod62.6.1526
Khosla, 2001, Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes, Biology of Reproduction, 64, 918, 10.1095/biolreprod64.3.918
Mann, 2004, Selective loss of imprinting in the placenta following preimplantation development in culture, Development, 131, 3727, 10.1242/dev.01241
Young, 2001, Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture, Nature Genetics, 27, 153, 10.1038/84769
Gicquel, 2003, In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene, American Journal of Human Genetics, 72, 1338, 10.1086/374824
Arnaud, 2005, Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction, Birth Defects Research. Part C, Embryo Today, 75, 81, 10.1002/bdrc.20039
Rossignol, 2006, The epigenetic imprinting defect of Beckwith-Wiedemann patients born following assisted reproductive technology is not restricted to the 11p15 region, Journal of Medical Genetics, 43, 902, 10.1136/jmg.2006.042135
MacLennan, 2004, Uteroplacental insufficiency alters DNA methylation, one-carbon metabolism, and histone acetylation in IUGR rats, Physiological Genomics, 18, 43, 10.1152/physiolgenomics.00042.2004
Lillycrop, 2005, Dietary protein restriction of pregnant rats induces and folic acid supplementation prevents epigenetic modification of hepatic gene expression in the offspring, The Journal of Nutrition, 135, 1382, 10.1093/jn/135.6.1382
Lillycrop, 2007, Induction of altered epigenetic regulation of the hepatic glucocorticoid receptor in the offspring of rats fed a protein-restricted diet during pregnancy suggests that reduced DNA methyltransferase-1 expression is involved in impaired DNA methylation and changes in histone modifications, The British Journal of Nutrition, 97, 1, 10.1017/S000711450769196X
Weaver, 2004, Epigenetic programming by maternal behavior, Nature Neuroscience, 7, 847, 10.1038/nn1276
Meaney, 2007, Epigenetic mechanisms of perinatal programming of hypothalamic–pituitary–adrenal function and health, Trends in Molecular Medicine, 13, 269, 10.1016/j.molmed.2007.05.003
Pham, 2003, Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney, American Journal of Physiology. Regulatory, Integrative and Comparative Physiology, 285, R962, 10.1152/ajpregu.00201.2003
Waterland, 2003, Transposable elements: targets for early nutritional effects on epigenetic gene regulation, Molecular and Cellular Biology, 23, 5293, 10.1128/MCB.23.15.5293-5300.2003
Dolinoy, 2006, Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome, Environmental Health Perspectives, 114, 567, 10.1289/ehp.8700
Waterland, 2006, Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus, Human Molecular Genetics, 15, 705, 10.1093/hmg/ddi484
Ingrosso, 2003, Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia, Lancet, 361, 1693, 10.1016/S0140-6736(03)13372-7
Drake, 2004, The intergenerational effects of fetal programming: non-genomic mechanisms for the inheritance of low birth weight and cardiovascular risk, The Journal of Endocrinology, 180, 1, 10.1677/joe.0.1800001
Gluckman, 2007, Non-genomic transgenerational inheritance of disease risk, Bioessays, 29, 145, 10.1002/bies.20522
Stewart, 1975, Twelve generations of marginal protein deficiency, The British Journal of Nutrition, 33, 233, 10.1079/BJN19750027
Drake, 2005, Intergenerational consequences of fetal programming by in utero exposure to glucocorticoids in rats, American Journal of Physiology. Regulatory, Integrative and Comparative Physiology, 288, R34, 10.1152/ajpregu.00106.2004
Chong, 2004, Epigenetic germline inheritance, Current Opinion in Genetics & Development, 14, 692, 10.1016/j.gde.2004.09.001
Morgan, 1999, Epigenetic inheritance at the agouti locus in the mouse, Nature Genetics, 23, 314, 10.1038/15490
Lane, 2003, Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse, Genesis, 35, 88, 10.1002/gene.10168
Anway, 2005, Epigenetic transgenerational actions of endocrine disruptors and male fertility, Science, 308, 1466, 10.1126/science.1108190
Chong, 2007, Heritable germline epimutation is not the same as transgenerational epigenetic inheritance, Nature Genetics, 39, 574, 10.1038/ng0507-574