Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

Abstract

Mest (also known as Peg1), an imprinted gene expressed only from the paternal allele during development, was disrupted by gene targeting in embryonic stem (ES) cells. The targeted mutation is imprinted and reversibly silenced by passage through the female germ line. Paternal transmission activates the targeted allele and causes embryonic growth retardation associated with reduced postnatal survival rates in mutant progeny. More significantly, Mest-deficient females show abnormal maternal behaviour and impaired placentophagia, a distinctive mammalian behaviour. Our results provide evidence for the involvement of an imprinted gene in the control of adult behaviour.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Mest targeting and derivation of Mest-deficient mice.
Figure 2: Growth retardation of Mest+/- mice.
Figure 3: Mest expression in the nervous system.
Figure 4: Reversible transcriptional silencing of the maternally inherited Mesttm1Lef allele.
Figure 5: Decreased reproductive fitness and abnormal maternal behaviour of Mest+/- females.

Similar content being viewed by others

Accession codes

Accessions

GenBank/EMBL/DDBJ

References

  1. Ainscough, J.F.-X. & Surani, M.A. Organization and control of imprinted genes: the common features. in Epigenetic Mechanisms of Gene Regulation (eds Russo, V.E.A., Martienssen, R.A. & Riggs, A.D.) 173–194 (CSHL Press, New York, 1996).

    Google Scholar 

  2. John, R.M. & Surani, M.A. Imprinted genes and regulation of gene expression by epigenetic inheritance. Curr. Opin. Cell Biol. 8, 348–353 ( 1996).

    Article  CAS  Google Scholar 

  3. Kaneko-Ishino, T. et al. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nature Genet. 11, 52–59 (1995).

    Article  CAS  Google Scholar 

  4. Sado, T., Nakajima, N., Tada, M. & Takagi, N. A novel mesoderm-specific cDNA isolated from a mouse embryonal carcinoma cell line. Develop. Growth Differ. 35, 551–560 (1993).

    Article  CAS  Google Scholar 

  5. Beechey, C.V. & Cattanach, B.M. Chromosome 6 and genetic imprinting . Mouse News Lett. 84, 82– 83 (1989).

    Google Scholar 

  6. Kobayashi, S. et al. Human PEG1/MEST, an imprinted gene on chromosome 7. Hum. Mol. Genet. 6, 781–786 (1997).

    Article  CAS  Google Scholar 

  7. Nishita, Y., Yoshida, I., Sado, T. & Takagi, N. Genomic imprinting and chromosomal localization of the human MEST gene. Genomics 36, 539–542 ( 1996).

    Article  CAS  Google Scholar 

  8. Riesewijk, A.M. et al. Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. Genomics 42 , 236–244 (1997).

    Article  CAS  Google Scholar 

  9. Spotila, L.D., Sereda, L. & Prockop, D.J. Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus. Am. J. Hum. Genet. 51, 1396–1405 (1992).

    CAS  PubMed  PubMed Central  Google Scholar 

  10. Spence, NM>J.E. et al. Uniparental disomy as a mechanism for human genetic disease. Am. J. Hum. Genet. 42, 217–226 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Voss, R. et al. Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans? Am. J. Hum. Genet. 45, 373–380 ( 1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  12. Lefebvre, L., Viville, S., Barton, S.C., Ishino, F. & Surani, M.A. Genomic structure and parent-of-origin-specific methylation of Peg1. Hum. Mol. Genet. 6, 1907–1915 (1997).

    Article  CAS  Google Scholar 

  13. Tada, M., Tada, T., Lefebvre, L., Barton, S.C. & Surani, M.A. Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells. EMBO J. 16, 6510–6520 (1997).

    Article  CAS  Google Scholar 

  14. Mountford, P. et al. Dicistronic targeting constructs: Reporters and modifiers of mammalian gene expression. Proc. Natl Acad. Sci. USA 91, 4303–4307 (1994).

    Article  CAS  Google Scholar 

  15. Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W. & Roder, J.C. Derivation of completely cell culture-derived mice from early passage embryonic stem cells. Proc. Natl Acad. Sci. USA 90, 8424–8428 ( 1993).

    Article  CAS  Google Scholar 

  16. Dickinson, C. & Keverne, E.B. Importance of noradrenergic mechanisms in the olfactory bulbs for the maternal behaviour of mice. Physiol. Behav. 43, 313–316 ( 1988).

    Article  CAS  Google Scholar 

  17. Ledbetter, D.H. & Engel, E. Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum. Mol. Genet. 4, 1757– 1764 (1995).

    Article  CAS  Google Scholar 

  18. Hoglund, P., Holmberg, C., de la Chapelle, A. & Kere, J. Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea. Am. J. Hum. Genet. 55, 747–752 ( 1994).

    CAS  PubMed  PubMed Central  Google Scholar 

  19. Langlois, S., Yong, S.L., Wilson, R.D., Kwong, L.C. & Kalousek, D.K. Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7. J. Med. Genet. 32, 871–875 (1995).

    Article  CAS  Google Scholar 

  20. Patton, M.A. Russell-Silver syndrome. J. Med. Genet. 25, 557–560 (1988).

    Article  CAS  Google Scholar 

  21. Eggermann, T. et al. Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy. Hum. Genet. 100, 415–419 (1997).

    Article  CAS  Google Scholar 

  22. Kotzot, D. et al. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Hum. Mol. Genet. 4, 583–587 (1995).

    Article  CAS  Google Scholar 

  23. Preece, M.A. et al. Maternal uniparental disomy 7 in Silver-Russell syndrome. J. Med. Genet. 34, 6–9 ( 1997).

    Article  CAS  Google Scholar 

  24. Miyoshi, N. et al. Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene. Proc. Natl Acad. Sci. USA 95, 1102– 1107 (1998).

    Article  CAS  Google Scholar 

  25. Moore, T. & Haig, D. Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet. 7, 45–49 (1991).

    Article  CAS  Google Scholar 

  26. Haig, D. & Graham, C. Genomic imprinting and the strange case of the insulin-like growth factor II receptor. Cell 64, 1045–1046 (1991).

    Article  CAS  Google Scholar 

  27. DeChiara, T.M., Robertson, E.J. & Efstratiadis, A. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849– 859 (1991).

    Article  CAS  Google Scholar 

  28. Numan, M. A neural circuity analysis of maternal behavior in the rat. Acta Paediatr. Suppl. 397, 19–28 (1994).

    Article  CAS  Google Scholar 

  29. Kristal, M.B. Enhancement of opioid-mediated analgesia: a solution to the enigma of placentophagia . Neurosci. Biobehav. Rev. 15, 425– 435 (1991).

    Article  CAS  Google Scholar 

  30. Bernardis, L.L. & Bellinger, L.L. The lateral hypothalamic area revisited: ingestive behavior. Neurosci. Biobehav. Rev. 20, 189–287 ( 1996).

    Article  CAS  Google Scholar 

  31. Franz, J.R., Leo, R.J., Steuer, M.A. & Kristal, M.B. Effects of hypothalamic knife cuts and experience on maternal behavior in the rat. Physiol. Behav. 38, 629–640 ( 1986).

    Article  CAS  Google Scholar 

  32. Brown, J.R., Ye, H., Bronson, R.T., Dikkes, > & Greenberg, M.E. A defect in nurturing in mice lacking the immediate early gene fosB. Cell 86, 297–309 ( 1996).

    Article  CAS  Google Scholar 

  33. Thomas, S.A. & Palmiter, R.D. Impaired maternal behavior in mice lacking norepinephrine and epinephrine. Cell 91 , 583–592 (1997).

    Article  CAS  Google Scholar 

  34. Fundele, R.H. & Surani, M.A. Experimental embryological analysis of genetic imprinting in mouse development. Dev. Genet. 15, 515–522 (1994).

    Article  CAS  Google Scholar 

  35. Allen, N.D. et al. Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior. Proc. Natl Acad. Sci. USA 92, 10782–10786 (1995).

    Article  CAS  Google Scholar 

  36. Cattanach, B.M. & Beechey, C.V. Autosomal and X-chromosome imprinting. Dev. Suppl. 63– 72 (1990).

  37. Cattanach, B.M. et al. A candidate model for Angelman syndrome in the mouse. Mamm. Genome 8, 472–478 (1997).

    Article  CAS  Google Scholar 

  38. Holm, V.A. et al. Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics 91, 398–402 ( 1993).

    CAS  PubMed  Google Scholar 

  39. Williams, C.A. et al. Angelman syndrome: consensus for diagnostic criteria. Am. J. Med. Genet. 56, 237–238 (1995).

    Article  CAS  Google Scholar 

  40. Lathe, R., Vilotte, J.L. & Clark, A.J. Plasmid and bacteriophage vectors for excision of intact inserts. Gene 57, 193– 201 (1987).

    Article  CAS  Google Scholar 

  41. Friedrich, G. & Soriano, P. Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice Genes Dev. 5, 1513–1523 (1991).

    Article  CAS  Google Scholar 

  42. Kikyo, N. et al. Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal chr 2. Dev. Biol. 190, 66–77 (1997).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank the members of our group for their help, especially J. Ainscough and R. John for their valuable comments on this work, J. Dixon for the IRES-βgeo construct pIFS and A. Nagy for the R1 ES cells. This work was supported by a grant from the Wellcome Trust to M.A.S. L.L. was a Research Fellow of the National Cancer Institute of Canada, supported with funds provided by the Terry Fox Run, and S.V. was supported by a Fellowship from EMBO.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Azim Surani.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lefebvre, L., Viville, S., Barton, S. et al. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 20, 163–169 (1998). https://doi.org/10.1038/2464

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/2464

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing