Journal article
Copy number variation analysis implicates the cell polarity gene glypican 5 as a human spina bifida candidate gene
Human molecular genetics, Vol.22(6), pp.1097-1111
03/15/2013
DOI: 10.1093/hmg/dds515
PMCID: PMC3578410
PMID: 23223018
Abstract
Neural tube defects (NTDs) are common birth defects of complex etiology. Family and population-based studies have confirmed a genetic component to NTDs. However, despite more than three decades of research, the genes involved in human NTDs remain largely unknown. We tested the hypothesis that rare copy number variants (CNVs), especially de novo germline CNVs, are a significant risk factor for NTDs. We used array-based comparative genomic hybridization (aCGH) to identify rare CNVs in 128 Caucasian and 61 Hispanic patients with non-syndromic lumbar-sacral myelomeningocele. We also performed aCGH analysis on the parents of affected individuals with rare CNVs where parental DNA was available (42 sets). Among the eight de novo CNVs that we identified, three generated copy number changes of entire genes. One large heterozygous deletion removed 27 genes, including PAX3, a known spina bifida-associated gene. A second CNV altered genes (PGPD8, ZC3H6) for which little is known regarding function or expression. A third heterozygous deletion removed GPC5 and part of GPC6, genes encoding glypicans. Glypicans are proteoglycans that modulate the activity of morphogens such as Sonic Hedgehog (SHH) and bone morphogenetic proteins (BMPs), both of which have been implicated in NTDs. Additionally, glypicans function in the planar cell polarity (PCP) pathway, and several PCP genes have been associated with NTDs. Here, we show that GPC5 orthologs are expressed in the neural tube, and that inhibiting their expression in frog and fish embryos results in NTDs. These results implicate GPC5 as a gene required for normal neural tube development.
Details
- Title: Subtitle
- Copy number variation analysis implicates the cell polarity gene glypican 5 as a human spina bifida candidate gene
- Creators
- Alexander G Bassuk - Department of Pediatrics, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USALakshmi B MuthuswamyRiley BolandTiffany L SmithAlissa M HulstrandHope NorthrupMatthew HakemanJason M DierdorffChristina K YungAbby LongRachel B BrouilletteKit Sing AuChristina GurnettDouglas W HoustonRobert A CornellJ Robert Manak
- Resource Type
- Journal article
- Publication Details
- Human molecular genetics, Vol.22(6), pp.1097-1111
- DOI
- 10.1093/hmg/dds515
- PMID
- 23223018
- PMCID
- PMC3578410
- NLM abbreviation
- Hum Mol Genet
- ISSN
- 0964-6906
- eISSN
- 1460-2083
- Publisher
- England
- Grant note
- GM083999 / NIGMS NIH HHS R01 DE021071 / NIDCR NIH HHS 1R01DE021071-01 / NIDCR NIH HHS
- Language
- English
- Date published
- 03/15/2013
- Academic Unit
- Neurology; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Biology; Craniofacial Anomalies Research Center; Neurology (Pediatrics); Dental Research; Internal Medicine
- Record Identifier
- 9983991997802771
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