Fertility and Sterility
Volume 93, Issue 8 , Pages 2507-2512, 15 May 2010

Messenger RNA expression of Pabpnl1 and Mbd3l2 genes in oocytes and cleavage embryos

  • Fernando Henrique Biase, Ph.D.

      Affiliations

    • Departamento de Ciências Básicas, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Ribeirão Preto, Brazil
    • Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil
  • ,
  • Lúcia Martelli, M.D., Ph.D.

      Affiliations

    • Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil
  • ,
  • Renato Puga, M.Sc.

      Affiliations

    • Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil
  • ,
  • Silvana Giuliatti, Ph.D.

      Affiliations

    • Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil
  • ,
  • Weruska Karyna Freitas Santos-Biase, M.Sc.

      Affiliations

    • Departamento de Ciências Básicas, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Ribeirão Preto, Brazil
  • ,
  • Giovana Krempel Fonseca Merighe, Ph.D.

      Affiliations

    • Departamento de Ciências Básicas, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Ribeirão Preto, Brazil
  • ,
  • Flávio Vieira Meirelles, Ph.D.

      Affiliations

    • Departamento de Ciências Básicas, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Ribeirão Preto, Brazil
    • Corresponding Author InformationReprint requests: Flávio Vieira Meirelles, Departamento de Ciências Básicas, USP-FZEA, Rua Duque de Caxias Norte, 225, Pirassununga–SP, 13635-900, Brazil (FAX: 55 19 3565 4117).

Received 28 January 2009; received in revised form 18 August 2009; accepted 19 August 2009. published online 12 October 2009.

Objective

To identify genes specifically expressed in mammalian oocytes using an in silico subtraction, and to characterize the mRNA patterns of selected genes in oocytes, embryos, and adult tissues.

Design

Comparison between oocyte groups and between early embryo stages.

Setting

Laboratories of embryo manipulation and molecular biology from Departamento de Genética (FMRP) and Departamento de Ciências Básicas (FZEA) - University of São Paulo.

Sample(s)

Oocytes were collected from slaughtered cows for measurements, in vitro fertilization, and in vitro embryo culture. Somatic tissue, excluding gonad and uterus tissue, was collected from male and female cattle.

Main Outcome Measure(s)

Messenger RNA levels of poly(A)-binding protein nuclear-like 1 (Pabpnl1) and methyl-CpG–binding domain protein 3–like 2 (Mbd3l2).

Result(s)

Pabpnl1 mRNA was found to be expressed in oocytes, and Mbd3l2 transcripts were present in embryos. Quantification of Pabpnl1 transcripts showed no difference in levels between good- and bad-quality oocytes before in vitro maturation (IVM) or between good-quality oocytes before and after IVM. However, Pabpnl1 transcripts were not detected in bad-quality oocytes after IVM. Transcripts of the Mbd3l2 gene were found in 4-cell, 8-cell, and morula-stage embryos, with the highest level observed in 8-cell embryos.

Conclusion(s)

Pabpnl1 gene expression is restricted to oocytes and Mbd3l2 to embryos. Different Pabpnl1 mRNA levels in oocytes of varying viability suggest an important role in fertility involving the oocyte potential for embryo development.

Key Words: Bovine, embryo, gene expression

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 F.H.B. has nothing to disclose. L.M. has nothing to disclose. R.P. has nothing to disclose. S.G. has nothing to disclose. W.K.F.S.B. has nothing to disclose. G.K.F.M. has nothing to disclose. F.V.M. has nothing to disclose.

 Supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Brazil.

PII: S0015-0282(09)03589-4

doi:10.1016/j.fertnstert.2009.08.051

Fertility and Sterility
Volume 93, Issue 8 , Pages 2507-2512, 15 May 2010