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Title: Genomic analysis of the Xp21 region around the RP3 locus

Journal Article · · American Journal of Human Genetics
OSTI ID:134451
 [1]; ;  [2]
  1. Massachusetts General Hospital, Boston, MA (United States)
  2. Children`s Hospital, Boston, MA (United States); and others

One form of X-linked retinitis pigmentosa has been localized by deletion and linkage analysis to proximal Xp21 near the OTC locus and the proximal breakpoint of the BB deletion. A deletion junction clone, previously isolated from this region, was used to initiate a series of bidirectional walks in a human genomic library in EMBL3A. A phage contig of nearly 70 kb has been cloned and systematically searched for conserved sequences and CA repeats. A number of unique sequences around the breakpoint have been sequenced and analyzed with exon identification programs. An HTF island was identified approximately 35 kb distal to the centromeric breakpoint of the BB deletion and several CA repeat-containing areas were found in the contig. Two YACs that contain the breakpoint and surrounding region were isolated. A phage sublibrary was constructed from one of the YACs and is being used to extend the contig map further centromeric. To isolate transcripts from the region, two rounds of cDNA selection from a combined short insert human retinal and fetal brain library were performed against the pooled phage clones from the contig and against the pooled phage from the YAC derived sublibrary. Among the selected cDNAs, several unique sequences have been identified and are currently being mapped and sequenced.

OSTI ID:
134451
Report Number(s):
CONF-941009-; ISSN 0002-9297; TRN: 95:005313-1185
Journal Information:
American Journal of Human Genetics, Vol. 55, Issue Suppl.3; Conference: 44. annual meeting of the American Society of Human Genetics, Montreal (Canada), 18-22 Oct 1994; Other Information: PBD: Sep 1994
Country of Publication:
United States
Language:
English