Epigenetic inheritance of metabolic state

Current Opinion in Genetics and Development

Volumn 27, Issue , 2014, Pages 43-47

  Somer, Rebecca A ^a   Thummel, Carl S ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMATIN; DIABETES MELLITUS; DNA METHYLATION; DROSOPHILA; EPIGENETICS; GENE EXPRESSION; HERITABILITY; HISTONE MODIFICATION; HUMAN; INHERITANCE; LIPID DIET; METABOLIC DISORDER; METABOLISM; NONHUMAN; NUTRITION; OBESITY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN RESTRICTION; REVIEW; ANIMAL; DISEASE MODEL; GENETIC EPIGENESIS; GENETICS; METABOLIC SYNDROME X;

ANIMALS; DIABETES MELLITUS; DISEASE MODELS, ANIMAL; EPIGENESIS, GENETIC; HUMANS; METABOLIC SYNDROME X; OBESITY;

EID: 84901036355     PISSN: 0959437X     EISSN: 18790380     Source Type: Journal    
DOI: 10.1016/j.gde.2014.03.008     Document Type: Review

References (37)

1. Ogden C.L., Carroll M.D., Kit B.K., Flegal K.M. Prevalence of Obesity in the United States, 2009-2010 2012, http://www.cdc.gov/obesity/index.html.
2. Prevention CfDCa National Diabetes Fact Sheet: National Estimates and General Information on Diabetes and Prediabetes in the United States 2011, http://www.cdc.gov/diabetes/pubs/factsheet11.htm.
3. Nelson V.R., Spiezio S.H., Nadeau J.H. Transgenerational genetic effects of the paternal Y chromosome on daughters' phenotypes. Epigenomics 2010, 2:513-521.
4. Lumey L.H., Stein A.D., Kahn H.S., Romijn J.A. Lipid profiles in middle-aged men and women after famine exposure during gestation: the Dutch Hunger Winter Families Study. Am J Clin Nutr 2009, 89:1737-1743.
5. de Rooij S.R., Painter R.C., Phillips D.I., Osmond C., Michels R.P., et al. Impaired insulin secretion after prenatal exposure to the Dutch famine. Diabetes Care 2006, 29:1897-1901.
6. Ravelli A.C., van Der Meulen J.H., Osmond C., Barker D.J., Bleker O.P. Obesity at the age of 50 y in men and women exposed to famine prenatally. Am J Clin Nutr 1999, 70:811-816.
7. Li Y., He Y., Qi L., Jaddoe V.W., Feskens E.J., et al. Exposure to the Chinese famine in early life and the risk of hyperglycemia and type 2 diabetes in adulthood. Diabetes 2010, 59:2400-2406.
8. Lillycrop K.A. Effect of maternal diet on the epigenome: implications for human metabolic disease. Proc Nutr Soc 2011, 70:64-72.
9. Hoile S.P., Lillycrop K.A., Thomas N.A., Hanson M.A., Burdge G.C. Dietary protein restriction during F0 pregnancy in rats induces transgenerational changes in the hepatic transcriptome in female offspring. PLoS ONE 2011, 6:e21668.
10. Burdge G.C., Phillips E.S., Dunn R.L., Jackson A.A., Lillycrop K.A. Effect of reduced maternal protein consumption during pregnancy in the rat on plasma lipid concentrations and expression of peroxisomal proliferator-activated receptors in the liver and adipose tissue of the offspring. Nutr Res 2004, 24:639-646.
11. Lillycrop K.A., Phillips E.S., Jackson A.A., Hanson M.A., Burdge G.C. Dietary protein restriction of pregnant rats induces and folic acid supplementation prevents epigenetic modification of hepatic gene expression in the offspring. J Nutr 2005, 135:1382-1386.
12. Bellinger L., Lilley C., Langley-Evans S.C. Prenatal exposure to a maternal low-protein diet programmes a preference for high-fat foods in the young adult rat. Br J Nutr 2004, 92:513-520.
13. Bellinger L., Sculley D.V., Langley-Evans S.C. Exposure to undernutrition in fetal life determines fat distribution, locomotor activity and food intake in ageing rats. Int J Obes (Lond) 2006, 30:729-738.
14. Langley-Evans S.C. Fetal programming of cardiovascular function through exposure to maternal undernutrition. Proc Nutr Soc 2001, 60:505-513.
15. Lucas A., Baker B.A., Desai M., Hales C.N. Nutrition in pregnant or lactating rats programs lipid metabolism in the offspring. Br J Nutr 1996, 76:605-612.
16. Jimenez-Chillaron J.C., Isganaitis E., Charalambous M., Gesta S., Pentinat-Pelegrin T., et al. Intergenerational transmission of glucose intolerance and obesity by in utero undernutrition in mice. Diabetes 2009, 58:460-468.
17. Duque-Guimaraes D.E., Ozanne S.E. Nutritional programming of insulin resistance: causes and consequences. Trends Endocrinol Metab 2013, 24:525-535.
18. Padmanabhan N., Jia D., Geary-Joo C., Wu X., Ferguson-Smith A.C., et al. Mutation in folate metabolism causes epigenetic instability and transgenerational effects on development. Cell 2013, 155:81-93.
19. Carone B.R., Fauquier L., Habib N., Shea J.M., Hart C.E., et al. Paternally induced transgenerational environmental reprogramming of metabolic gene expression in mammals. Cell 2010, 143:1084-1096.
20. Ng S.F., Lin R.C., Laybutt D.R., Barres R., Owens J.A., Morris M.J. Chronic high-fat diet in fathers programs beta-cell dysfunction in female rat offspring. Nature 2010, 467:963-966.
21. Fullston T., Ohlsson Teague E.M., Palmer N.O., DeBlasio M.J., Mitchell M., et al. Paternal obesity initiates metabolic disturbances in two generations of mice with incomplete penetrance to the F2 generation and alters the transcriptional profile of testis and sperm microRNA content. FASEB J 2013, 27:4226-4243.
22. Yazbek S.N., Spiezio S.H., Nadeau J.H., Buchner D.A. Ancestral paternal genotype controls body weight and food intake for multiple generations. Hum Mol Genet 2010, 19:4134-4144.
23. Matzkin L.M., Johnson S., Paight C., Markow T.A. Preadult parental diet affects offspring development and metabolism in Drosophila melanogaster. PLoS ONE 2013, 8:e59530.
24. Buescher J.L., Musselman L.P., Wilson C.A., Lang T., Keleher M., et al. Evidence for transgenerational metabolic programming in Drosophila. Dis Model Mech 2013, 6:1123-1132.
25. Kirchner H., Osler M.E., Krook A., Zierath J.R. Epigenetic flexibility in metabolic regulation: disease cause and prevention?. Trends Cell Biol 2013, 23:203-209.
26. Petruk S., Sedkov Y., Johnston D.M., Hodgson J.W., Black K.L., et al. TrxG and PcG proteins but not methylated histones remain associated with DNA through replication. Cell 2012, 150:922-933.
27. Francis N.J., Follmer N.E., Simon M.D., Aghia G., Butler J.D. Polycomb proteins remain bound to chromatin and DNA during DNA replication in vitro. Cell 2009, 137:110-122.
28. Hajkova P., Ancelin K., Waldmann T., Lacoste N., Lange U.C., et al. Chromatin dynamics during epigenetic reprogramming in the mouse germ line. Nature 2008, 452:877-881.
29. Hajkova P., Erhardt S., Lane N., Haaf T., El-Maarri O., et al. Epigenetic reprogramming in mouse primordial germ cells. Mech Dev 2002, 117:15-23.
30. Lee J., Inoue K., Ono R., Ogonuki N., Kohda T., et al. Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells. Development 2002, 129:1807-1817.
31. de Vanssay A., Bouge A.L., Boivin A., Hermant C., Teysset L., et al. Paramutation in Drosophila linked to emergence of a piRNA-producing locus. Nature 2012, 490:112-115.
32. Ronsseray S., Boivin A., Anxolabehere D. P-Element repression in Drosophila melanogaster by variegating clusters of P-lacZ-white transgenes. Genetics 2001, 159:1631-1642.
33. Castel S.E., Martienssen R.A. RNA interference in the nucleus: roles for small RNAs in transcription, epigenetics and beyond. Nat Rev Genet 2013, 14:100-112.
34. Grentzinger T., Armenise C., Brun C., Mugat B., Serrano V., et al. piRNA-mediated transgenerational inheritance of an acquired trait. Genome Res 2012, 22:1877-1888.
35. Ashe A., Sapetschnig A., Weick E.M., Mitchell J., Bagijn M.P., et al. piRNAs can trigger a multigenerational epigenetic memory in the germline of C. elegans. Cell 2012, 150:88-99.
36. Shirayama M., Seth M., Lee H.C., Gu W., Ishidate T., et al. piRNAs initiate an epigenetic memory of nonself RNA in the C. elegans germline. Cell 2012, 150:65-77.
37. Buckley B.A., Burkhart K.B., Gu S.G., Spracklin G., Kershner A., et al. A nuclear Argonaute promotes multigenerational epigenetic inheritance and germline immortality. Nature 2012, 489:447-451.