Most genes on the X chromosome undergo ''inactivation,'' being transcr
ibed from only one copy in female somatic cells, but several human gen
es have been shown to be expressed from both the active and the otherw
ise inactivated homologue. To assess further the fraction and location
of genes that escape inactivation, we have analyzed the inactivation
status of a set of 73 expressed sequence tags that were derived from t
he sequencing of cDNA collections and mapped to the X chromosome. Of 3
3 that were expressed in cultured cells, as assessed by reverse transc
ription and PCR, 4 (about 12%) were transcribed from both the active a
nd the inactive X chromosome, Two, RPS4 and PCTAIRE1, are already know
n to escape inactivation; the other 2, of unknown function, include a
short cDNA with a full open reading frame and a transcript with no det
ectable open reading frame. They map, respectively, to Xp11.3-p11.4 an
d Xp22.2; both regions were previously reported to encode sequences tr
anscribed from the inactive X. Neither transcript has a corresponding
sequence on the Y. Thus, they exhibit double dosage in females compare
d to males, and inactivation status may be inconsequential for these t
ranscribed sequences. (C) 1997 Academic Press.