X chromosome-specific cDNA arrays:: identification of genes that escape from X-inactivation and other applications

被引:53
作者
Sudbrak, R
Wieczorek, G
Nuber, UA
Mann, W
Kirchner, R
Erdogan, F
Brown, CJ
Wöhrle, D
Sterk, P
Kalscheuer, VM
Berger, W
Lehrach, H
Ropers, HH
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Univ British Columbia, Dept Med Genet, Vancouver, BC, Canada
[3] Univ Ulm, Dept Med Genet, D-89069 Ulm, Germany
[4] European Bioinformat Inst, Cambridge, England
关键词
D O I
10.1093/hmg/10.1.77
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mutant alleles are frequently characterized by low expression levels. Therefore, cDNA array-based gene expression profiling may be a promising strategy for identifying gene defects underlying monogenic disorders. To study the potential of this approach, we have generated an X chromosome-specific microarray carrying 2423 cloned cDNA fragments, which represent up to 1317 different X-chromosomal genes. As a prelude to testing cell lines from patients with X-linked disorders, this array was used as a hybridization probe to compare gene expression profiles in lymphoblastoid cell lines from normal males, females and individuals with supernumerary X chromosomes. Measurable hybridization signals were obtained for more than half of the genes represented on the chip. A total of 53 genes showed elevated expression levels in cells with multiple X chromosomes and many of these were found to escape X-inactivation. Moreover, the detection of a male-viable deletion encompassing three genes illustrates the utility of this array for the identification of small unbalanced chromosome rearrangements.
引用
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页码:77 / 83
页数:7
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