R. Sultana et al., THE MOUSE SB1.8 GENE LOCATED AT THE DISTAL END OF THE X-CHROMOSOME ISSUBJECT TO X-INACTIVATION, Human molecular genetics, 4(2), 1995, pp. 257-263
The mouse homolog of the human DXS423E (SB1.8) gene has been isolated
by screening a mouse cDNA library. Like its human counterpart, the mou
se Sb1.8 gene is X-linked, as shown by Southern blot analysis and by i
n situ hybridization to metaphase chromosomes. Sb1.8 was sublocalized
to band F of the mouse X chromosome, distal to Alas2 and proximal to D
XPas1, which confirms a region of conservation between band Xp11.21-p1
1.22 in human and band XF in mouse. In situ hybridization also showed
that the Smcx (Xe169) gene maps near Sb1.8 in band F. The Sb1.8 gene w
as shown to be highly conserved in mammals; partial DNA sequence analy
sis indicates 92% identity between the mouse and human genes. In contr
ast to the human DXS423E gene, the mouse Sb1.8 gene is subject to X in
activation, as shown by restriction enzyme and sequence analysis of mR
NA from mice with Searle's translocation (T(X;16)16H). Absence of Sb1.
8 expression from the inactive mouse X chromosome in vitro was confirm
ed by analysis of a cell line (Hobmski) in which the M.spretus X chrom
osome is inactivated. The Sb1.8 gene is a new member of a group of gen
es that escape X inactivation in human, but are inactivated in mouse.