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.

Erasure of MLH1 methylation in spermatozoa—implications for epigenetic inheritance

To the Editor:

Recent discourse concerning the mode of inheritance of germline epimutations has centered on whether the altered epigenetic state may be passed directly through the gametes to offspring (bona fide transgenerational epigenetic inheritance), or whether, alternatively, the epigenetic mark is cleared in the germ cells and reimposed on the affected allele after fertilization1,2,3,4. Pivotal to this debate is the report by Suter et al. that a male individual (TT) with a soma-wide MLH1 epimutation retained the methylation mark in a small proportion (≤1%) of his spermatozoa5. Spermatozoa are notoriously difficult to separate from somatic cells, and neither FACS nor microscopy provides absolute reassurance that the methylated MLH1 alleles were not derived from the proband's somatic tissues, in which the epimutation was widespread2. Because a stringent molecular control was not included in the original analysis, this remained a possibility. The SNRPN gene is monoallelically expressed from the paternally inherited allele and methylated specifically on the maternal allele in somatic tissues, but it is unmethylated in mammalian spermatozoa6, allowing any source of methylation from somatic cells to be traced. We have now reassessed the original spermatozoa sample from individual TT, this time including the SNRPN control, using two quantitative techniques: the same colony-hybridization method originally employed5 and the more recently developed fluorescence-based real-time methylation-specific PCR f-MSP method7. Irrespective of technique, we detected low levels of MLH1 methylation consistent with the original report, but we found the level of SNRPN methylation marginally exceeded that of MLH1, indicating the methylation most likely derived from residual somatic DNA (data presented in the Addendum to the original report by Suter et al.). Futhermore, we acquired a new spermatozoa sample from individual TTthat was devoid of MLH1 methylation using f-MSP. In light of this new evidence, we suggest that the data originally reported should not be proffered as evidence that MLH1 methylation persists in male germ cells5. The data presented here, and in our more recent study7, show that the spermatozoa from individuals with soma-wide MLH1 epimutations are, in fact, devoid of MLH1 methylation. The epigenetic manifestations of this defect are thus likely to be cleared from the affected allele during spermatogenesis. This demethylation is most likely to occur contemporaneously with the removal of epigenetic marks from imprinted genes in primordial germ cells. Although this argues against the notion that MLH1 epimutations are directly transmissible through the male germ line through 'transgenerational epigenetic inheritance,' it does not necessarily nullify the risk of paternal transmission of this defect to offspring. Epimutations may be re-established postzygotically, albeit associated with a single parental allele and present in all somatic cell types. A precedent for this caveat is the paternal transmission of microdeletions of the SNURF-SNRPN imprinting center on the paternal 15q12 allele, which cause the normally unmethylated allele to assume the fully methylated imprint of the maternal allele across the imprinted 15q12 region in the somatic tissues of offspring, resulting in Prader-Willi syndrome8. In such cases, the spermatozoa of fathers harboring the imprinting center microdeletions are unmethylated, and the allele only becomes fully methylated postzygotically6; hence the methylation status of the spermatozoa themselves provides no indication of transmission risk. Although we have shown that MLH1 epimutations are unlikely to be caused by a fully penetrant genetic alteration in cis7, the possibility that genetic interplay between a cis- or trans-acting modifier predisposes the allele to epimutation cannot be ruled out at present. Our recent report of stochastic maternal transmission of an MLH1 epimutation indicates that the 'signal' underlying this defect is passed directly through the female germ line to a proportion of offspring7. Whether this takes the form of a co-inherited genetic factor or a fundamental epigenetic aberration in the oocyte remains to be elucidated. Should the latter be the case, the risk of inheritance of MLH1 epimutations will depend on the sex of the transmitting parent, and we would expect to see a significant bias in the rate of maternal transmission. However, until the mechanism underlying MLH1 epimutations is identified, we caution against using the epigenetic state in spermatozoa as a predictor of paternal inheritance risk. The children of epimutation carriers should be offered testing irrespective of the sex of the affected parent.

References

  1. 1

    Chong, S., Youngson, N.A. & Whitelaw, E. Heritable germline epimutation is not the same as transgenerational epigenetic inheritance. Nat. Genet. 39, 574–575 (2007).

    CAS  Article  Google Scholar 

  2. 2

    Horsthemke, B. Heritable germline epimutations in humans. Nat. Genet. 39, 573–574 (2007).

    CAS  Article  Google Scholar 

  3. 3

    Suter, C.M. & Martin, D.I. Reply to “Heritable germline epimutation is not the same as transgenerational epigenetic inheritance”. Nat. Genet. 39, 575–576 (2007).

    CAS  Article  Google Scholar 

  4. 4

    Suter, C.M. & Martin, D.I. Inherited epimutation or a haplotypic basis for the propensity to silence? Nat. Genet. 39, 573 (2007).

    CAS  Article  Google Scholar 

  5. 5

    Suter, C.M., Martin, D.I. & Ward, R.L. Germline epimutation of MLH1 in individuals with multiple cancers. Nat. Genet. 36, 497–501 (2004).

    CAS  Article  Google Scholar 

  6. 6

    El-Maarri, O. et al. Maternal methylation imprints on human chromosome 15 are established during or after fertilization. Nat. Genet. 27, 341–344 (2001).

    CAS  Article  Google Scholar 

  7. 7

    Hitchins, M.P. et al. Inheritance of a cancer-associated MLH1 germ-line epimutation. N. Engl. J. Med. 356, 697–705 (2007).

    CAS  Article  Google Scholar 

  8. 8

    Reed, M.L. & Leff, S.E. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome. Nat. Genet. 6, 163–167 (1994).

    CAS  Article  Google Scholar 

Download references

Author information

Affiliations

Authors

Corresponding author

Correspondence to Robyn L Ward.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Hitchins, M., Ward, R. Erasure of MLH1 methylation in spermatozoa—implications for epigenetic inheritance. Nat Genet 39, 1289 (2007). https://doi.org/10.1038/ng1107-1289

Download citation

Further reading

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