Toward expression mapping of albinism-deafness syndrome (ADFN) locus on chromosome Xq26

Citation
Ank. Jacob et al., Toward expression mapping of albinism-deafness syndrome (ADFN) locus on chromosome Xq26, SOM CELL M, 24(2), 1998, pp. 135-140
Citations number
11
Categorie Soggetti
Molecular Biology & Genetics
Journal title
SOMATIC CELL AND MOLECULAR GENETICS
ISSN journal
07407750 → ACNP
Volume
24
Issue
2
Year of publication
1998
Pages
135 - 140
Database
ISI
SICI code
0740-7750(199803)24:2<135:TEMOAS>2.0.ZU;2-B
Abstract
We have employed a direct cDNA selection methodology to isolate transcribed sequences encoded in the human chromosomal interval Xq26 that contains the gene for X-chromosome linked albinism deafness syndrome (ADFN). ADFN had b een previously, mapped to an 8 centi Morgan region on chromosome Xq26. We h ave constructed six cDNA libraries specific to six YACs mapping To a 1.5 mb span at the distal boundary of the ADFN locus. The YAC specific libraries were characterized for the presence of unique cDNAs. We have identified 15 transcribed sequences from the selected cDNA libraries, These cDNAs matched to three well characterized sequences corresponding to steroid 5-alpha red uctase, ribosomal protein L28, and a short transcript that has been shown t o be expressed in human brain cortex. Seven of the cDNAs matched to express ed sequence tags or other sequences of unknown function, and Jive cDNAs sha red no homology with sequences in the public data bases. Each one of these sequences was represented as 3-10 clones in the set that was subjected to s equencing. Further characterization of these transcribed sequences may indi cate potential candidates responsible for ADFN. We have discussed the utili ty of cDNA selection methodology in assembling transcript maps and identify ing potential candidates for genetic deafness.