YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28

被引:49
作者
PALMIERI, G
ROMANO, G
CICCODICOLA, A
CASAMASSIMI, A
CAMPANILE, C
ESPOSITO, T
CAPPA, V
LANIA, A
JOHNSON, S
REINBOLD, R
POUSTKA, A
SCHLESSINGER, D
DURSO, M
机构
[1] INT INST GENET & BIOPHYS,I-80125 NAPLES,ITALY
[2] WASHINGTON UNIV,DEPT MOLEC MICROBIOL,ST LOUIS,MO 63110
[3] GERMAN CANC RES CTR,W-6900 HEIDELBERG,GERMANY
关键词
D O I
10.1006/geno.1994.1592
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 hybridization probes and were extensive enough to be aligned and oriented by published genetic linkage and somatic cell hybrid panel data. Selected YACs from the entire region were mapped with five rare-cutter restriction enzymes to infer the position of putative CpG islands indicative of gene locations; 48 such sites were identified by the near-coincidence of at least three rare-cutter sites. The analysis defined three subregions 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 G6PD gene, that is variably and poorly cloned, but contains a high concentration 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 subtelomeric DNA region that shows extensive homology to Yq DNA. (C) 1994 Academic Press, Inc.
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页码:149 / 158
页数:10
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