Trans-generational epistasis between Dnd1Ter and other modifier genes controls susceptibility to testicular germ cell tumors.

The genetic basis for susceptibility to testicular germ cell tumors (TGCTs) has been remarkably elusive. Although TGCTs are the most common cancer in young men and have an unusually strong familial risk, only one low-frequency susceptibility gene has been identified for this highly multigenic trait. In tests to determine whether pairs of genetic variants act epistatically to modulate susceptibility in the 129/Sv mouse model of spontaneous TGCTs, we discovered an unusual mode of inheritance that involved interactions between different genes in different generations. Any of six genetic variants, in either the female or male parent interacted with the Dnd1(Ter) mutation in male offspring to significantly increase both the frequency of affected Ter/+ males and the proportion of bilateral cases. Trans-generational epistasis is a novel mode of epigenetic inheritance that could account for the difficulty of finding TGCT susceptibility genes in humans and might represent a mechanism for transmitting information about genetic and environmental conditions from parents to offspring through the germline.

[1]  J. Nadeau,et al.  DNA pooling as a quick method for finding candidate linkages in multigenic trait analysis: an example involving susceptibility to germ cell tumors , 2009, Mammalian Genome.

[2]  Jason D. Heaney,et al.  Testicular germ cell tumors in mice: new ways to study a genetically complex trait. , 2008, Methods in molecular biology.

[3]  C. Naughton,et al.  Epigenetic Transgenerational Actions of Endocrine Disruptors and Male Fertility , 2006 .

[4]  R. Braun,et al.  Pathway to Totipotency: Lessons from Germ Cells , 2006, Cell.

[5]  David I. K. Martin,et al.  Germ-line epigenetic modification of the murine Avy allele by nutritional supplementation , 2006, Proceedings of the National Academy of Sciences.

[6]  N. Navaratnam,et al.  An Overview of Cytidine Deaminases , 2006, International journal of hematology.

[7]  Alan Horwich,et al.  Testicular germ-cell cancer , 2006, The Lancet.

[8]  K. Hemminki,et al.  Familial risks in testicular cancer as aetiological clues. , 2006, International journal of andrology.

[9]  M. Stratton,et al.  Genome-wide linkage screen for testicular germ cell tumour susceptibility loci. , 2006, Human molecular genetics.

[10]  J. Olsen,et al.  Male reproductive disorders in humans and prenatal indicators of estrogen exposure. A review of published epidemiological studies. , 2006, Reproductive toxicology.

[11]  Reuven Agami,et al.  A genetic screen implicates miRNA-372 and miRNA-373 as oncogenes in testicular germ cell tumors. , 2006, Cell.

[12]  M. Pike,et al.  The Y deletion gr/gr and susceptibility to testicular germ cell tumor. , 2005, American journal of human genetics.

[13]  B. Hales,et al.  Epigenetic programming in the preimplantation rat embryo is disrupted by chronic paternal cyclophosphamide exposure , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[14]  J. Nadeau,et al.  The Ter mutation in the dead end gene causes germ cell loss and testicular germ cell tumours , 2005, Nature.

[15]  S. Safe Clinical correlates of environmental endocrine disruptors , 2005, Trends in Endocrinology & Metabolism.

[16]  Katherine M. Tucker,et al.  Somatic mutations of KIT in familial testicular germ cell tumours , 2004, British Journal of Cancer.

[17]  U. Pichlmeier,et al.  Clinical epidemiology of testicular germ cell tumors , 2004, World Journal of Urology.

[18]  J. Nadeau,et al.  Enhancers and suppressors of testicular cancer susceptibility in single- and double-mutant mice. , 2004, Genetics.

[19]  D. Bartel MicroRNAs Genomics, Biogenesis, Mechanism, and Function , 2004, Cell.

[20]  S. Fosså,et al.  Stem cell factor receptor (c-KIT) codon 816 mutations predict development of bilateral testicular germ-cell tumors. , 2003, Cancer research.

[21]  Y. Bergman,et al.  Oct-3/4 is a dose-dependent oncogenic fate determinant. , 2003, Cancer cell.

[22]  P. Sharp,et al.  Embryonic stem cell-specific MicroRNAs. , 2003, Developmental cell.

[23]  T. Matsuda,et al.  Increasing incidence of testicular cancer worldwide: a review. , 2003, The Journal of urology.

[24]  A. Bird,et al.  Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals , 2003, Nature Genetics.

[25]  J. Nadeau,et al.  Testicular cancer susceptibility in the 129.MOLF-Chr19 mouse strain: additive effects, gene interactions and epigenetic modifications. , 2003, Human molecular genetics.

[26]  V. Rakyan,et al.  Transgenerational epigenetic inheritance , 2003, Current Biology.

[27]  A. Chompret The Li-Fraumeni syndrome. , 2002, Biochimie.

[28]  N. Skakkebaek,et al.  Are Male Reproductive Disorders a Common Entity? , 2001 .

[29]  J. Nadeau,et al.  Sensitized polygenic trait analysis. , 2001, Trends in genetics : TIG.

[30]  G. Eklund,et al.  Analysis of hereditary component of cancer by use of a familial index by site , 2001, The Lancet.

[31]  Yumiko Sasaoka,et al.  Novel growth factor supporting survival of murine primordial germ cells: evidence from conditioned medium of ter fetal gonadal somatic cells , 2001, Molecular reproduction and development.

[32]  N. Skakkebaek,et al.  Testicular dysgenesis syndrome: an increasingly common developmental disorder with environmental aspects , 2001, Human reproduction.

[33]  N. Skakkebaek,et al.  Are male reproductive disorders a common entity? The testicular dysgenesis syndrome. , 2001, Annals of the New York Academy of Sciences.

[34]  A. Levine,et al.  A male germ cell tumor-susceptibility-determining locus, pgct1, identified on murine chromosome 13. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[35]  N. Sherman,et al.  Molecular Cloning of Apobec-1 Complementation Factor, a Novel RNA-Binding Protein Involved in the Editing of Apolipoprotein B mRNA , 2000, Molecular and Cellular Biology.

[36]  I. Khrebtukova,et al.  Alternative processing of the human and mouse raly genes(1). , 1999, Biochimica et biophysica acta.

[37]  J. Nadeau,et al.  Susceptibility to testicular germ-cell tumours in a 129.MOLF-Chr 19 chromosome substitution strain , 1999, Nature Genetics.

[38]  Ş. Güran,et al.  Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family. , 1999, Cancer genetics and cytogenetics.

[39]  Carlos Cordon-Cardo,et al.  Pten is essential for embryonic development and tumour suppression , 1998, Nature Genetics.

[40]  K. Kinzler,et al.  The Genetic Basis of Human Cancer , 1997 .

[41]  L. Donehower,et al.  Effects of genetic background on tumorigenesis in p53‐deficient mice , 1995, Molecular carcinogenesis.

[42]  S. Buetow Epidemiology of testicular cancer. , 1995, Epidemiologic reviews.

[43]  L. Stubbs,et al.  A molecular model for the genetic and phenotypic characteristics of the mouse lethal yellow (Ay) mutation. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[44]  L. Donehower,et al.  Genetic background alters the spectrum of tumors that develop in p53‐deficient mice , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[45]  D. Malkin,et al.  p53 and the Li-Fraumeni syndrome. , 1993, Cancer genetics and cytogenetics.

[46]  L. Donehower,et al.  Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours , 1992, Nature.

[47]  D. Forman,et al.  Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis. , 1992, British Journal of Cancer.

[48]  L. Strong,et al.  Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. , 1990, Science.

[49]  M. Noguchi,et al.  A recessive mutation (ter) causing germ cell deficiency and a high incidence of congenital testicular teratomas in 129/Sv-ter mice. , 1985, Journal of the National Cancer Institute.

[50]  W. Silvers The Coat Colors of Mice , 1979, Springer New York.

[51]  L. C. Stevens A new inbred subline of mice (129-terSv) with a high incidence of spontaneous congenital testicular teratomas. , 1973, Journal of the National Cancer Institute.

[52]  L. C. Stevens The biology of teratomas. , 1967, Advances in morphogenesis.

[53]  W. E. Heston,et al.  INCREASE OF INDUCED SKIN TUMORS IN THE MOUSE BY THE LETHAL YELLOW GENE (AY). , 1963, Journal of the National Cancer Institute.

[54]  K. Hummel,et al.  A description of spontaneous congenital testicular teratomas in strain 129 mice. , 1957, Journal of the National Cancer Institute.