ISOLATION OF COSMID AND CDNA CLONES IN THE REGION SURROUNDING THE BTK GENE AT XQ21.3-Q22

被引:38
作者
VORECHOVSKY, I
VETRIE, D
HOLLAND, J
BENTLEY, DR
THOMAS, K
ZHOU, JN
NOTARANGELO, LD
PLEBANI, A
FONTAN, G
OCHS, HD
HAMMARSTROM, L
SIDERAS, P
SMITH, CIE
机构
[1] UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV MED & MOLEC GENET,LONDON SE1 9RT,ENGLAND
[2] SANGER CTR,CAMBRIDGE CB10 1RQ,CAMBS,ENGLAND
[3] UNIV BRESCIA,DEPT PEDIAT,I-25123 BRESCIA,ITALY
[4] HOSP LA PAZ,IMMUNOL UNIT,E-28048 MADRID,SPAIN
[5] UNIV WASHINGTON,SCH MED,DEPT PEDIAT,DIV IMMUNOL RHEUMATOL,SEATTLE,WA 98195
[6] UMEA UNIV,APPL CELL & MOLEC BIOL UNIT,S-90187 UMEA,SWEDEN
关键词
D O I
10.1006/geno.1994.1310
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
A regional physical and transcription map involving yeast artificial chromosomes (YACs), cosmids, and cDNAs has been constructed for Xq21.3-q22 around the gene BTK (formerly atk or BPK) defective in X-linked agammaglobulinemia (XLA). With a positional cloning strategy employing direct cDNA selection, novel cDNAs were found to cluster in the region of approximately 100 kb flanking the XLA and alpha-galactosidase A loci. While these widely expressed transcripts are in the area known to contain CpG islands, a less evolutionarily conserved gene, located more than 130 kb distal of DXS178, maps to cosmid clones that could not be digested with rare-cutting restriction enzymes. The presence of transcribed sequences flanking the BTK allowed us to investigate their involvement in complex XLA phenotypes. Southern blot analysis using cDNA clones isolated from this region permitted us to exclude a contiguous deletion syndrome as an underlying defect in three patients with XLA and associated growth hormone deficiency. A single XLA patient with torsion dystonia and cosegregating X-linked deafness has been found with a deletion in the 3' part of BTK extending centromerically into the flanking expressed sequence DXS1274E. This suggests a possible involvement of the DXS1274E in this phenotype. The GenBank accession numbers for novel cDNA sequences are as follows: DXS1269E (L20773), DXS1271E (UO1923), DXS1273E (UO1925), and DXS1274E (UO1922). (C) 1994 Academic Press, Inc.
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页码:517 / 524
页数:8
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