Fertility and Sterility
Volume 94, Issue 5 , Pages 1728-1733, October 2010

Alterations in sperm DNA methylation patterns at imprinted loci in two classes of infertility

  • Saher Sue Hammoud, B.S.

      Affiliations

    • Andrology and IVF Laboratories, Division of Urology, Department of Surgery, School of Medicine, University of Utah, Salt Lake City, Utah
    • Department of Physiology, School of Medicine, University of Utah, Salt Lake City, Utah
  • ,
  • Jahnvi Purwar, B.S.

      Affiliations

    • Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah
  • ,
  • Christian Pflueger, M.S.

      Affiliations

    • Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah
  • ,
  • Bradley R. Cairns, Ph.D.

      Affiliations

    • Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah
    • Howard Hughes Medical Institute, University of Utah School of Medicine, Salt Lake City, Utah
  • ,
  • Douglas T. Carrell, Ph.D.

      Affiliations

    • Andrology and IVF Laboratories, Division of Urology, Department of Surgery, School of Medicine, University of Utah, Salt Lake City, Utah
    • Department of Physiology, School of Medicine, University of Utah, Salt Lake City, Utah
    • Department of Obstetrics and Gynecology, School of Medicine, University of Utah, Salt Lake City, Utah
    • Corresponding Author InformationReprint requests: Douglas T. Carrell, Ph.D., University of Utah IVF and Andrology Laboratories, 675 Arapeen Drive, Suite 205, Salt Lake City, UT 84108 (FAX: 801-581-6127).

Received 8 April 2009; received in revised form 5 August 2009; accepted 8 September 2009. published online 02 November 2009.

Objective

To evaluate the associations between proper protamine incorporation and DNA methylation at imprinted loci.

Design

Experimental research study.

Setting

Research laboratory.

Patient(s)

Three populations were tested—abnormal protamine patients, oligozoospermic patients, and fertile donors.

Intervention(s)

The CpG methylation patterns were examined at seven imprinted loci sequenced: LIT1, MEST, SNRPN, PLAGL1, PEG3, H19, and IGF2.

Main Outcome Measure(s)

The DNA methylation patterns were analyzed using bisulfite sequencing. The percentage of methylation was compared between fertile and infertile patients displaying abnormal protamination.

Result(s)

At six of the seven imprinted genes, the overall DNA methylation patterns at their respective differentially methylated regions were significantly altered in both infertile patient populations. When comparing the severity of methylation alterations among infertile patients, the oligozoospermic patients were significantly affected at mesoderm-specific transcript (MEST), whereas abnormal protamine patients were affected at KCNQ1, overlapping transcript 1 (LIT1), and at small nuclear ribonucleoprotein polypeptide N (SNRPN).

Conclusion(s)

Patients with male factor infertility had significantly increased methylation alteration at six of seven imprinted loci tested, with differences in significance observed between oligozoospermic and abnormal protamine patients. This could suggest that risk of transmission of epigenetic alterations may be different with diagnoses. However, this study does not provide a causal link for epigenetic inheritance of imprinting diseases, but does show significant association between male factor infertility and alterations in sperm DNA methylation at imprinted loci.

Key Words: Imprinting, Beckwith-Wiedemann syndrome and epigenetic alterations, Angelman syndrome, chromatin, assisted reproductive technology, IVF, ICSI, oligozoospermic, protamines

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 S.S.H. has nothing to disclose. J.P. has nothing to disclose. C.P. has nothing to disclose. B.R.C. has nothing to disclose. D.T.C. has nothing to disclose.

 Saher Sue Hammoud and Jahnvi Purwar contributed equally.

PII: S0015-0282(09)03689-9

doi:10.1016/j.fertnstert.2009.09.010

Fertility and Sterility
Volume 94, Issue 5 , Pages 1728-1733, October 2010