Literature DB >> 17406783

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

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.

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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


  4 in total

1.  Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH).

Authors:  Shin Hayashi; Nobuhiko Okamoto; Yasutsugu Chinen; Jun-ichi Takanashi; Yoshio Makita; Akira Hata; Issei Imoto; Johji Inazawa
Journal:  Hum Genet       Date:  2011-07-07       Impact factor: 4.132

2.  Evidence for disease penetrance relating to CNV size: Pelizaeus-Merzbacher disease and manifesting carriers with a familial 11 Mb duplication at Xq22.

Authors:  C M B Carvalho; M Bartnik; D Pehlivan; P Fang; J Shen; J R Lupski
Journal:  Clin Genet       Date:  2011-06-20       Impact factor: 4.438

3.  A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation.

Authors:  Aritoshi Iida; Eri Takeshita; Shunichi Kosugi; Yoichiro Kamatani; Yukihide Momozawa; Michiaki Kubo; Eiji Nakagawa; Kenji Kurosawa; Ken Inoue; Yu-Ichi Goto
Journal:  Hum Genome Var       Date:  2018-12-05

4.  Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement.

Authors:  Oleg A Shchelochkov; M Lance Cooper; Zhishuo Ou; Sandra Peacock; Svetlana A Yatsenko; Chester W Brown; Ping Fang; Pawel Stankiewicz; Sau Wai Cheung
Journal:  Mol Cytogenet       Date:  2008-07-25       Impact factor: 2.009

  4 in total

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