Abstract
Csn3
(
Cops3
) maps to the mouse chromosome 11 region syntenic to the common deletion interval for the Smith-Magenis syndrome, a contiguous gene deletion syndrome. It encodes the third subunit of an eight-subunit protein complex, the COP9 signalosome (CSN), which controls a wide variety of molecules of different functions. Mutants of this complex caused lethality at early development of both plants and
Drosophila melanogaster
. CSN function in vivo in mammals is unknown. We disrupted the murine
Csn3
gene in three independent ways with insertional vectors, including constructing a ≈3-Mb inversion chromosome. The heterozygous mice appeared normal, although the protein level was reduced.
Csn3
−/−
embryos arrested after 5.5 days postcoitum (dpc) and resorbed by 8.5 dpc. Mutant embryos form an abnormal egg cylinder which does not gastrulate. They have reduced numbers of epiblast cells, mainly due to increased cell death. In the
Csn3
−/−
mice, subunit 8 of the COP9 complex was not detected by immunohistochemical techniques, suggesting that the absence of Csn3 may disrupt the entire COP9 complex. Therefore,
Csn3
is important for maintaining the integrity of the COP9 signalosome and is crucial to maintain the survival of epiblast cells and thus the development of the postimplantation embryo in mice.
