One hundred nineteen YACs were assembled into 6 contigs spanning about
7.1 Mb of Xq28. The contigs were formatted with 65 STSs and 136 hybri
dization probes and were extensive enough to be aligned and oriented b
y published genetic linkage and somatic cell hybrid panel data. Select
ed YACs from the entire region were mapped with five rare-cutter restr
iction enzymes to infer the position of putative CpG islands indicativ
e of gene locations; 48 such sites were identified by the near-coincid
ence of at least three rare-cutter sites. The analysis defined three s
ubregions of Xq28: 4 Mb of moderate GC and CpG island content from the
Xq27 border through the GABRA locus; 1.5 to 2 Mb, extending to the G6
PD gene, that is variably and poorly cloned, but contains a high conce
ntration of CpG islands and GC; and about 1.5 Mb between G6PD and the
telomere, which is generally low in CpG and GC levels, including a sub
telomeric DNA region that shows extensive homology to Yq DNA. (C) 1994
Academic Press, Inc.