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Quantitative Analysis of Protein Expression to Study Lineage Specification in Mouse Preimplantation Embryos
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Published on: February 22, 2016

EMG1 is essential for mouse pre-implantation embryo development.

Xiaoli Wu1, Sumit Sandhu, Nehal Patel

  • 1Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Canada.

BMC Developmental Biology
|September 23, 2010
PubMed
Summary

Essential for mitotic growth 1 (EMG1) is crucial for early mouse embryonic development. Complete loss of EMG1 function in mice causes pre-implantation lethality, highlighting its essential role in mammalian development and Bowen-Conradi syndrome.

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Area of Science:

  • Developmental Biology
  • Molecular Genetics

Background:

  • Essential for mitotic growth 1 (EMG1) is a conserved nucleolar protein vital for ribosome biogenesis in yeast.
  • Mutations in human EMG1 cause Bowen-Conradi syndrome (BCS), a severe developmental disorder.

Purpose of the Study:

  • To investigate the role of EMG1 in mammalian development using a mouse model.
  • To understand how EMG1 deficiency may lead to Bowen-Conradi syndrome.

Main Methods:

  • Examined Emg1 expression during mouse embryonic development.
  • Generated and characterized mice with a null mutation for Emg1 using gene targeting.

Main Results:

  • Emg1 is broadly expressed in early development, with specific patterns later.
  • Loss of EMG1 function arrested embryonic development before the blastocyst stage.
  • Emg1-/- embryos showed defects in cell lineage specification and nucleologenesis; p53 loss did not rescue lethality.

Conclusions:

  • Emg1 is essential for mouse pre-implantation development, consistent with its role in yeast.
  • Findings support that partial EMG1 deficiency causes Bowen-Conradi syndrome.
  • Complete EMG1 deficiency is incompatible with live birth.