Al. Brown et Gf. Kay, Bex1, a gene with increased expression in parthenogenetic embryos, is a member of a novel gene family on the mouse X chromosome, HUM MOL GEN, 8(4), 1999, pp. 611-619
Parthenogenetic and normal blastocysts were compared using differential dis
play analysis as a means to identify new imprinted genes, A single gene was
identified with increased expression in parthenogenetic blastocysts, sugge
sting it might be an imprinted gene expressed from the maternally inherited
allele, The gene, named Bex1 (brain expressed X-linked gene), maps near Pi
p on the mouse X chromosome and to Xq22 in humans. Database homology search
es revealed two additional uncharacterized cDNAs similar to Bex1 that were
named Bex2 and Bex3. Allele-specific expression analysis of Bex1 using Fl b
lastocysts indicated an excess of transcript expressed from the maternally
inherited allele compared with the paternally inherited allele, This excess
level of transcript derived from the maternally inherited allele may be du
e to imprinted X inactivation of the paternally inherited allele in the ext
raembryonic lineages of female embryos rather than a result of genomic impr
inting.