The imprinted polycomb group gene Sfmbt2 is required for trophoblast maintenance and placenta development

Author:

Miri Kamelia1,Latham Keith2,Panning Barbara3,Zhong Zhisheng2,Andersen Angela3,Varmuza Susannah1

Affiliation:

1. Department of Cell and Systems Biology, University of Toronto, 25 Harbord Sreet, Toronto, Ontario M5S 3G5, Canada.

2. The Fels Institute of Cancer Research and Molecular Biology and Department of Biochemistry, Temple University School of Medicine, 3307 North Broad Street, Philadelphia, PA 19140, USA.

3. Biochemistry and Biophysics Department, University of California at San Francisco, Genentech Hall, 600 16th Street, San Francisco, CA 94158-2517, USA.

Abstract

Imprinted genes play important roles in placenta development and function. Parthenogenetic embryos, deficient in paternally expressed imprinted genes, lack extra-embryonic tissues of the trophoblast lineage. Parthenogenetic trophoblast stem cells (TSCs) are extremely difficult to derive, suggesting that an imprinted gene(s) is necessary for TSC establishment or maintenance. In a candidate study, we were able to narrow the list to one known paternally expressed gene, Sfmbt2. We show that mouse embryos inheriting a paternal Sfmbt2 gene trap null allele have severely reduced placentae and die before E12.5 due to reduction of all trophoblast cell types. We infected early embryos with lentivirus vectors expressing anti-Sfmbt2 shRNAs and found that TSC derivation was significantly reduced. Together, these observations support the hypothesis that loss of SFMBT2 results in defects in maintenance of trophoblast cell types necessary for development of the extra-embryonic tissues, the placenta in particular.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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