| Literature DB >> 17406783 |
Shin Hayashi1,2,3, Shozo Honda1,2,3, Maki Minaguchi1,3, Yoshio Makita4, Nobuhiko Okamoto5, Rika Kosaki6, Torayuki Okuyama6, Issei Imoto1,7,3, Shuki Mizutani2, Johji Inazawa8,9,10,11.
Abstract
The human chromosome X is closely associated with congenital disorders and mental retardation (MR), because it contains a significantly higher number of genes than estimated from the proportion in the human genome. We constructed a high-density and high-resolution human chromosome X array (X-tiling array) for comparative genomic hybridization (CGH). The array contains a total of 1,001 bacterial artificial chromosome (BACs) throughout chromosome X except pseudoautosomal regions and two BACs specific for Y. In four hybridizations using DNA samples from healthy males, the ratio of each spotted DNA was scattered between -3SD and 3SD, corresponding to a log(2) ratio of -0.35 and 0.35, respectively. Using DNA samples from patients with known congenital disorders, our X-tiling array was proven to discriminate one-copy losses and gains together with their physical sizes, and also to estimate the percentage of a mosaicism in a patient with mos 45,X[13]/46,X,r(X)[7]. Furthermore, array-CGH in a patient with atypical Schinzel-Giedion syndrome disclosed a 1.1-Mb duplication at Xq22.3 including a part of the IL1RAPL2 gene as a likely causative aberration. The results indicate our in-house X-tiling array to be useful for the identification of cryptic copy-number aberrations containing novel genes responsible for diseases such as congenital disorders and X-linked MR.Entities:
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Year: 2007 PMID: 17406783 DOI: 10.1007/s10038-007-0127-4
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172