Isolation of expressed sequences encoded by the human Xq terminal portion using microclone probes generated by laser microdissection.

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Citation

Yokoi H, Hadano S, Kogi M, Kang X, Wakasa K, Ikeda JE

Isolation of expressed sequences encoded by the human Xq terminal portion using microclone probes generated by laser microdissection.

Genomics. 1994 Apr;20(3):404-11. doi: 10.1006/geno.1994.1194.

PubMed ID
8034313 [ View in PubMed
]
Abstract

The genes that cause a variety of neurologic and neuromuscular disorders have been mapped to the distal region of Xq. In an effort to isolate genes from this area, a regional genomic library of the distal 30% of Xq was constructed from a single metaphase spread by means of laser microdissection and single unique primer-polymerase chain reaction. Using pooled probes of 1000 clones from the genomic library, human brain cDNA libraries were screened for expressed sequences encoded by this region. From the 250,000 cDNA clones screened so far, 10 nonoverlapping sequences that mapped back to the target portion were isolated. The complete nucleotide sequences of these cDNA clones have been determined. Analysis of the sequences indicates that none has significant similarity to previously characterized primate genes. One sequence mapping to Xq27.3-qter contained an open reading frame of 281 amino acids and was expressed in every tissue tested. This gene, as well as others isolated in this manner, may prove to be a candidate gene for heritable disorders mapping to this region.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
V-type proton ATPase subunit S1Q15904Details