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Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7.
- Source :
-
Stem cell research [Stem Cell Res] 2018 Oct; Vol. 32, pp. 73-77. Date of Electronic Publication: 2018 Sep 06. - Publication Year :
- 2018
-
Abstract
- CHRNA7, encoding the neuronal alpha7 nicotinic acetylcholine receptor (a7nAChR), is highly expressed in the brain, particularly in the hippocampus. It is situated in the 15q13.3 chromosome region, frequently associated with a Copy Number Variation (CNV), which causes its duplication or deletion. The clinical significance of CHRNA7 duplications is unknown so far, but there are several research data suggesting that they may be pathogenic, with reduced penetrance. We have produced an iPS cell line from a single healthy donor's fibroblasts carrying a 15q13.3 CNV, including CHRNA7 in order to study the exact role of this CNV during the neurodevelopment.<br /> (Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Adult
Cells, Cultured
Embryoid Bodies cytology
Female
Humans
Karyotype
Real-Time Polymerase Chain Reaction
Chromosomes, Human, Pair 15 genetics
DNA Copy Number Variations genetics
Induced Pluripotent Stem Cells cytology
Induced Pluripotent Stem Cells metabolism
alpha7 Nicotinic Acetylcholine Receptor genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1876-7753
- Volume :
- 32
- Database :
- MEDLINE
- Journal :
- Stem cell research
- Publication Type :
- Academic Journal
- Accession number :
- 30218896
- Full Text :
- https://doi.org/10.1016/j.scr.2018.09.002