PUBLICATION
Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes
- Authors
- Carvalho, C.M., Vasanth, S., Shinawi, M., Russell, C., Ramocki, M.B., Brown, C.W., Graakjaer, J., Skytte, A.B., Vianna-Morgante, A.M., Krepischi, A.C., Patel, G.S., Immken, L., Aleck, K., Lim, C., Cheung, S.W., Rosenberg, C., Katsanis, N., Lupski, J.R.
- ID
- ZDB-PUB-141203-70
- Date
- 2014
- Source
- American journal of human genetics 95: 565-78 (Journal)
- Registered Authors
- Katsanis, Nicholas
- Keywords
- none
- MeSH Terms
-
- Abnormalities, Multiple/genetics*
- Acyl-CoA Dehydrogenase, Long-Chain/genetics
- Adaptor Proteins, Signal Transducing/genetics
- Animals
- Asialoglycoprotein Receptor/genetics
- Base Sequence
- Cell Line
- Chromosome Breakpoints
- Chromosome Deletion
- Chromosomes, Human, Pair 17/genetics
- Flow Cytometry
- Gene Dosage/genetics*
- Humans
- Immunohistochemistry
- Intellectual Disability/genetics*
- Microcephaly/genetics*
- Microtubule-Associated Proteins/genetics
- Molecular Sequence Data
- Phosphoproteins/genetics
- Retrospective Studies
- Sequence Analysis, DNA
- Smith-Magenis Syndrome
- Syndrome
- Zebrafish
- PubMed
- 25439725 Full text @ Am. J. Hum. Genet.
Citation
Carvalho, C.M., Vasanth, S., Shinawi, M., Russell, C., Ramocki, M.B., Brown, C.W., Graakjaer, J., Skytte, A.B., Vianna-Morgante, A.M., Krepischi, A.C., Patel, G.S., Immken, L., Aleck, K., Lim, C., Cheung, S.W., Rosenberg, C., Katsanis, N., Lupski, J.R. (2014) Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes. American journal of human genetics. 95:565-78.
Abstract
The 17p13.1 microdeletion syndrome is a recently described genomic disorder with a core clinical phenotype of intellectual disability, poor to absent speech, dysmorphic features, and a constellation of more variable clinical features, most prominently microcephaly. We identified five subjects with copy-number variants (CNVs) on 17p13.1 for whom we performed detailed clinical and molecular studies. Breakpoint mapping and retrospective analysis of published cases refined the smallest region of overlap (SRO) for microcephaly to a genomic interval containing nine genes. Dissection of this phenotype in zebrafish embryos revealed a complex genetic architecture: dosage perturbation of four genes (ASGR1, ACADVL, DVL2, and GABARAP) impeded neurodevelopment and decreased dosage of the same loci caused a reduced mitotic index in vitro. Moreover, epistatic analyses in vivo showed that dosage perturbations of discrete gene pairings induce microcephaly. Taken together, these studies support a model in which concomitant dosage perturbation of multiple genes within the CNV drive the microcephaly and possibly other neurodevelopmental phenotypes associated with rearrangements in the 17p13.1 SRO.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping