Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2

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dc.contributor.authorGuo, Tingwei
dc.contributor.authorDiacou, Alexander
dc.contributor.authorNomaru, Hiroko
dc.contributor.authorMcDonald-McGinn, Donna M.
dc.contributor.authorHestand, Matthew
dc.contributor.authorDemaerel, Wolfram
dc.contributor.authorZhang, Liangtian
dc.contributor.authorZhao, Yingjie
dc.contributor.authorUjueta, Francisco
dc.contributor.authorShan, Jidong
dc.contributor.authorMontagna, Cristina
dc.contributor.authorZheng, Deyou
dc.contributor.authorCrowley, Terrence B.
dc.contributor.authorKushan-Wells, Leila
dc.contributor.authorBearden, Carrie E.
dc.contributor.authorKates, Wendy R.
dc.contributor.authorGothelf, Doron
dc.contributor.authorSchneider, Maude
dc.contributor.authorEliez, Stephan
dc.contributor.authorBreckpot, Jeroen
dc.contributor.authorSwillen, Ann
dc.contributor.authorVorstman, Jacob
dc.contributor.authorZackai, Elaine
dc.contributor.authorBenavides, Felipe
dc.contributor.authorRepetto, Gabriela
dc.contributor.authorEmanuel, Beverly S.
dc.contributor.authorBassett, Anne S.
dc.contributor.authorVermeesch, Joris R.
dc.contributor.authorMarshall, Christian R.
dc.contributor.authorMorrow, Bernice E.
dc.date.accessioned2021-08-27T20:23:18Z
dc.date.available2021-08-27T20:23:18Z
dc.date.issued2018
dc.description.abstractRecurrent, de novo, meiotic non-allelic homologous recombination events between low copy repeats, termed LCR22s, leads to the 22q11.2 deletion syndrome (22q11.2DS; velo-cardio-facial syndrome/DiGeorge syndrome). Although most 22q11.2DS patients have a similar sized 3 million base pair (Mb), LCR22A-D deletion, some have nested LCR22A-B or LCR22A-C deletions. Our goal is to identify additional recurrent 22q11.2 deletions associated with 22q11.2DS, serving as recombination hotspots for meiotic chromosomal rearrangements. Here, using data from Affymetrix 6.0 microarrays on 1680 22q11.2DS subjects, we identified what appeared to be a nested proximal 22q11.2 deletion in 38 (2.3%) of them. Using molecular and haplotype analyses from 14 subjects and their parent(s) with available DNA, we found essentially three types of scenarios to explain this observation. In eight subjects, the proximal breakpoints occurred in a small sized 12 kb LCR distal to LCR22A, referred to LCR22Aþ, resulting in LCR22Aþ-B or LCR22Aþ-D deletions. Six of these eight subjects had a nested 22q11.2 deletion that occurred during meiosis in a parent carrying a benign 0.2 Mb duplication of the LCR22A-LCR22Aþregion with a breakpoint in LCR22Aþ. Another six had a typical de novo LCR22A-D deletion on one allele and inherited the LCR22A-Aþduplication from the other parent thus appearing on microarrays to have a nested deletion. LCR22Aþmaps to an evolutionary breakpoint between mice and humans and appears to serve as a local hotspot for chromosome rearrangements on 22q11.2.es
dc.identifier.citationHuman Molecular Genetics, 2018, Vol. 27, No. 7 1150–1163es
dc.identifier.urihttp://dx.doi.org/10.1093/hmg/ddy028es
dc.identifier.urihttp://hdl.handle.net/11447/4519
dc.language.isoenes
dc.titleDeletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2es
dc.typeArticlees

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