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Classic Bladder Exstrophy: Frequent 22q11.21 Duplications and Definition of a 414 kb Phenocritical Region

Draaken, Markus (author)
Institute of Human Genetics, University of Bonn, Germany
Baudisch, Friederike (author)
Timmermann, Bernd (author)
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Kuhl, Heiner (author)
Kerick, Martin (author)
Proske, Judith (author)
Wittler, Lars (author)
Pennimpede, Tracie (author)
Ebert, Anne-Karoline (author)
Roesch, Wolfgang (author)
Stein, Raimund (author)
Bartels, Enrika (author)
von Lowtzow, Catharina (author)
Boemers, Thomas M. (author)
Herms, Stefan (author)
Gearhart, John P. (author)
Lakshmanan, Yegappan (author)
Clementson Kockum, Christina (author)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
Holmdahl, Gundela (author)
Karolinska Institutet
Läckgren, Göran (author)
Uppsala universitet,Institutionen för kvinnors och barns hälsa,Barnkirurgi/Christofferson
Nordenskjold, Agnetha (author)
Karolinska Institutet
Boyadjiev, Simeon A. (author)
Herrmann, Bernhard G. (author)
Noethen, Markus M. (author)
Ludwig, Michael (author)
Reutter, Heiko (author)
Institute of Human Genetics, University of Bonn, Germany
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 (creator_code:org_t)
2014-04-25
2014
English.
In: Birth Defects Research. Part A: Clinical and Molecular Teratology. - : Wiley. - 1542-0760 .- 1542-0752. ; 100:6, s. 512-517
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Classic bladder exstrophy (CBE) is the most common form of the bladder exstrophy and epispadias complex. Previously, we and others have identified four patients with a duplication of 22q11.21 among a total of 96 unrelated CBE patients. Methods: Here, we investigated whether this chromosomal aberration was commonly associated with CBE/bladder exstrophy and epispadias complex in an extended case-control sample. Multiplex ligation-dependent probe amplification and microarray-based analysis were used to identify 22q11.21 duplications in 244 unrelated bladder exstrophy and epispadias complex patients (including 217 CBE patients) and 665 healthy controls. Results: New duplications of variable size were identified in four CBE patients and one control. Pooling of our previous and present data (eight duplications in 313 CBE patients) yielded a combined odds ratio of 31.86 (95% confidence interval, 4.24-1407.97). Array-based sequence capture and high-throughput targeted re-sequencing established that all breakpoints resided within the low-copy repeats 22A to 22D. Comparison of the eight duplications revealed a 414 kb phenocritical region harboring 12 validated RefSeq genes. Characterization of these 12 candidate genes through whole-mount in situ hybridization of mouse embryos at embryonic day 9.5 suggested that CRKL, THAP7, and LZTR1 are CBE candidate genes. Conclusion: Our data suggest that duplication of 22q11.21 increases CBE risk and implicate a phenocritical region in disease formation. (C) 2014 Wiley Periodicals, Inc.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

chromosome 22q11.2
duplication
bladder exstrophy and epispadias
complex (BEEC)
classic bladder exstrophy (CBE)
copy number variation

Publication and Content Type

art (subject category)
ref (subject category)

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