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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

Authors :
Elisa Maria Turco
Ersilia Vinci
Filomena Altieri
Daniela Ferrari
Barbara Torres
Marina Goldoni
Giuseppe Lamorte
Ada Maria Tata
Gianluigi Mazzoccoli
Diana Postorivo
Matteo Della Monica
Laura Bernardini
Angelo Luigi Vescovi
Jessica Rosati
Source :
Stem Cell Research, Vol 32, Iss , Pp 73-77 (2018)
Publication Year :
2018
Publisher :
Elsevier, 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.

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
18735061
Volume :
32
Issue :
73-77
Database :
Directory of Open Access Journals
Journal :
Stem Cell Research
Publication Type :
Academic Journal
Accession number :
edsdoj.2be36cd9f65f42a4812c977fa079ede6
Document Type :
article
Full Text :
https://doi.org/10.1016/j.scr.2018.09.002