Expression of imprinted genes related to Beckwith-Wiedemann syndrome in human oocytes and preimplantation embryos

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):265-7.

Abstract

Objective: To investigate the expression of imprinted genes related to Beckwith-Wiedemann syndrome (BWS) in human oocytes and preimplantation embryos for understanding the relationship between assisted reproductive technology (ART) and BWS.

Methods: Using nested reverse transcription-PCR to analyze the expression of P57KIP2, LIT1, TSSC3 in human oocytes and preimplantation embryos.

Results: Transcripts of P57KIP2 were detected in human oocytes and at all stages of preimplantation embryos. LIT1 was expressed only in stages of 8-cell and blastocyst. Transcripts of TSSC3 could not be detected in human oocytes and preimplantation embryos.

Conclusion: Transcripts of P57KIP2 and LIT1, imprinted genes related to BWS, were detected in human preimplantation development; ART might affect the epigenetics of imprinted genes in early embryogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Beckwith-Wiedemann Syndrome / genetics*
  • Blastocyst / metabolism*
  • Cyclin-Dependent Kinase Inhibitor p57 / genetics
  • Female
  • Gene Expression Profiling*
  • Genomic Imprinting / genetics*
  • Humans
  • Nuclear Proteins / genetics
  • Oocytes / metabolism*
  • Potassium Channels, Voltage-Gated / genetics
  • Pregnancy
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Cyclin-Dependent Kinase Inhibitor p57
  • KCNQ1OT1 long non-coding RNA, human
  • Nuclear Proteins
  • Potassium Channels, Voltage-Gated
  • TSSC3 protein