Back to Search Start Over

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.

Authors :
Turco EM
Vinci E
Altieri F
Ferrari D
Torres B
Goldoni M
Lamorte G
Tata AM
Mazzoccoli G
Postorivo D
Della Monica M
Bernardini L
Vescovi AL
Rosati J
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.)

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