Disruption of Ini1 leads to peri-implantation lethality and tumorigenesis in mice
Guidi, Cynthia J. ; Sands, Arthur T. ; Zambrowicz, Brian P. ; Turner, Tod K. ; Demers, Delia A. ; Webster, William ; Smith, Thomas W. ; Imbalzano, Anthony N. ; Jones, Stephen N.
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Abstract
SNF5/INI1 is a component of the ATP-dependent chromatin remodeling enzyme family SWI/SNF. Germ line mutations of INI1 have been identified in children with brain and renal rhabdoid tumors, indicating that INI1 is a tumor suppressor. Here we report that disruption of Ini1 expression in mice results in early embryonic lethality. Ini1-null embryos die between 3.5 and 5.5 days postcoitum, and Ini1-null blastocysts fail to hatch, form the trophectoderm, or expand the inner cell mass when cultured in vitro. Furthermore, we report that approximately 15% of Ini1-heterozygous mice present with tumors, mostly undifferentiated or poorly differentiated sarcomas. Tumor formation is associated with a loss of heterozygocity at the Ini1 locus, characterizing Ini1 as a tumor suppressor in mice. Thus, Ini1 is essential for embryo viability and for repression of oncogenesis in the adult organism.
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Mol Cell Biol. 2001 May;21(10):3598-603. Link to article on publisher's site