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The imprinted polycomb group gene Sfmbt2 is required for trophoblast maintenance and placenta development
Author(s) -
Kamelia Miri,
Keith E. Latham,
Barbara Panning,
Zhisheng Zhong,
Angela A. Andersen,
Susannah Varmuza
Publication year - 2013
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.096511
Subject(s) - trophoblast , biology , genomic imprinting , placenta , inner cell mass , embryonic stem cell , embryo , embryogenesis , gene , genetics , imprinting (psychology) , parthenogenesis , allele , microbiology and biotechnology , stem cell , blastocyst , gene expression , dna methylation , fetus , pregnancy
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.

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