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Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation

Abstract

Imprinted genes are expressed from only one of the parental chromosomes and are marked epigenetically by DNA methylation and histone modifications1,2,3,4,5,6,7,8,9. The imprinting center 2 (IC2) on mouse distal chromosome 7 is flanked by several paternally repressed genes, with the more distant ones imprinted exclusively in the placenta. We found that most of these genes lack parent-specific DNA methylation, and genetic ablation of methylation does not lead to loss of their imprinting in the trophoblast (placenta). The silent paternal alleles of the genes are marked in the trophoblast by repressive histone modifications (dimethylation at Lys9 of histone H3 and trimethylation at Lys27 of histone H3), which are disrupted when IC2 is deleted, leading to reactivation of the paternal alleles. Thus, repressive histone methylation is recruited by IC2 (potentially through a noncoding antisense RNA) to the paternal chromosome in a region of at least 700 kb and maintains imprinting in this cluster in the placenta, independently of DNA methylation. We propose that an evolutionarily older imprinting mechanism limited to extraembryonic tissues was based on histone modifications, and that this mechanism was subsequently made more stable for use in embryonic lineages by the recruitment of DNA methylation.

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Figure 1: CpG island methylation of the IC2 imprinted gene cluster.
Figure 2: Analysis of imprinting in Dmnt1−/− conceptuses and conceptuses with paternal deletion of IC2.
Figure 3: Analysis of allele-specific histone modifications in placenta with paternal deletion of IC2.
Figure 4: Model of the epigenetic control of imprinting of the IC2 cluster.

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References

  1. Reik, W. & Walter, J. Genomic imprinting: parental influence on the genome. Nat. Rev. Genet. 2, 21–32 (2001).

    Article  CAS  Google Scholar 

  2. Ferguson-Smith, A.C. & Surani, M.A. Imprinting and the epigenetic asymmetry between parental genomes. Science 293, 1086–1089 (2001).

    Article  CAS  Google Scholar 

  3. Sleutels, F. & Barlow, D.P. The origins of genomic imprinting in mammals. Adv. Genet. 46, 119–163 (2002).

    Article  CAS  Google Scholar 

  4. Verona, R.I., Mann, M.R. & Bartolomei, M.S. Genomic imprinting: intricacies of epigenetic regulation in clusters. Annu. Rev. Cell. Dev. Biol. 19, 237–259 (2003).

    Article  CAS  Google Scholar 

  5. Li, E., Beard, C. & Jaenisch, R. Role for DNA methylation in genomic imprinting. Nature 366, 362–365 (1993).

    Article  CAS  Google Scholar 

  6. Bourc'his, D., Xu, G.L., Lin, C.S., Bollman, B. & Bestor, T.H. Dnmt3L and the establishment of maternal genomic imprints. Science 294, 2536–2539 (2001).

    Article  CAS  Google Scholar 

  7. Kaneda, M. et al. Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting. Nature 429, 900–903 (2004).

    Article  CAS  Google Scholar 

  8. Grandjean, V., O'Neill, L., Sado, T., Turner, B. & Ferguson-Smith, A. Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain. FEBS Lett. 488, 165–169 (2001).

    Article  CAS  Google Scholar 

  9. Fournier, C. et al. Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes. EMBO J. 21, 6560–6570 (2002).

    Article  CAS  Google Scholar 

  10. Howell, C.Y. et al. Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene. Cell 104, 829–838 (2001).

    Article  CAS  Google Scholar 

  11. Shemer, R., Birger, Y., Riggs, A.D. & Razin, A. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc. Natl. Acad. Sci. USA 94, 10267–10272 (1997).

    Article  CAS  Google Scholar 

  12. Dao, D. et al. Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting. Hum. Mol. Genet. 8, 1337–1352 (1999).

    Article  CAS  Google Scholar 

  13. Caspary, T., Cleary, M.A., Baker, C.C., Guan, X.J. & Tilghman, S.M. Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol. Cell. Biol. 18, 3466–3474 (1998).

    Article  CAS  Google Scholar 

  14. Tanaka, M. et al. Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation. Mech. Dev. 87, 129–142 (1999).

    Article  CAS  Google Scholar 

  15. Engemann, S. et al. Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting. Hum. Mol. Genet. 9, 2691–2706 (2000).

    Article  CAS  Google Scholar 

  16. Fitzpatrick, G.V., Soloway, P.D. & Higgins, M.J. Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat. Genet. 32, 426–431 (2002).

    Article  CAS  Google Scholar 

  17. Yatsuki, H. et al. Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region. Genome Res. 12, 1860–1870 (2002).

    Article  CAS  Google Scholar 

  18. Lei, H. et al. De novo DNA cytosine methyltransferase activities in mouse embryonic stem cells. Development 122, 3195–3205 (1996).

    CAS  PubMed  Google Scholar 

  19. Sado, T. et al. X inactivation in the mouse embryo deficient for Dnmt1: distinct effect of hypomethylation on imprinted and random X inactivation. Dev. Biol. 225, 294–303 (2000).

    Article  CAS  Google Scholar 

  20. Umlauf, D et al. Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. Nat. Genet. advance online publication, 31 October 2004 (doi:10.1038/ngXXX).

  21. Mager, J., Montgomery, N.D., de Villena, F.P. & Magnuson, T. Genome imprinting regulated by the mouse Polycomb group protein Eed. Nat. Genet. 33, 502–507 (2003).

    Article  CAS  Google Scholar 

  22. Wutz, A. & Jaenisch, R. A shift from reversible to irreversible X inactivation is triggered during ES cell differentiation. Mol. Cell 5, 695–705 (2000).

    Article  CAS  Google Scholar 

  23. Heard, E. Recent advances in X-chromosome inactivation. Curr. Opin. Cell. Biol. 16, 247–255 (2004).

    Article  CAS  Google Scholar 

  24. Zwart, R., Sleutels, F., Wutz, A., Schinkel, A.H. & Barlow, D.P. Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes. Genes Dev. 15, 2361–2366 (2001).

    Article  CAS  Google Scholar 

  25. Kanduri, C. et al. A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator. J. Biol. Chem. 277, 18106–18110 (2002).

    Article  CAS  Google Scholar 

  26. Wilkins, J.F. & Haig, D. What good is genomic imprinting: the function of parent-specific gene expression. Nat. Rev. Genet. 4, 359–368 (2003).

    Article  CAS  Google Scholar 

  27. Killian, J.K. et al. M6P/IGF2R imprinting evolution in mammals. Mol. Cell 5, 707–716 (2000).

    Article  CAS  Google Scholar 

  28. Cleary, M.A. et al. Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice. Nat. Genet. 29, 78–82 (2001).

    Article  CAS  Google Scholar 

  29. Paulsen, M. et al. Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse. Hum. Mol. Genet. 9, 1829–1841 (2000).

    Article  CAS  Google Scholar 

  30. Smilinich, N.J. et al. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc. Natl. Acad. Sci. USA 96, 8064–8069 (1999).

    Article  CAS  Google Scholar 

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Acknowledgements

We thank E. Li for Dnmt1 knockout mice, Y. Zhang for antibodies, G. Fitzpatrick for help with the KvDMR1 knockout, F. Cerrato for help with allele-specific RT-PCR and F. Santos and G. Kelsey for advice and discussion. This work was supported by the Biotechnology and Biological Sciences Research Council and the Medical Research Council (to W.R. and W.D.) and by the Cancer Centre Support Grant and the National Cancer Institute (to M.H.).

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Correspondence to Wolf Reik.

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Supplementary Fig. 1

CpG island methylation of IC2 imprinted gene cluster in mouse embryonic and extraembryonic cell lineages. (PDF 572 kb)

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Lewis, A., Mitsuya, K., Umlauf, D. et al. Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nat Genet 36, 1291–1295 (2004). https://doi.org/10.1038/ng1468

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