Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/31098
Title: MT-CYB sequencing analysis in frontotemporal lobar degeneration
Authors: Gonçalves, Mónica Silveira 
Orientador: Grazina, Maria Manuela Monteiro
Keywords: degeneração frontotemporal lobar; DNA mitocondrial; variações na sequência; o gene MT- CYB
Issue Date: 2014
Abstract: Frontotemporal lobar degeneration (FTLD) is the second most common cause for dementia before 65 years of age. FTLD comprises variants with a very diverging spectrum, regarding the clinical presentation, genetic features, and neuropathology. In the last decades remarkable progresses have been achieved in terms of genetic causes and their relation with neuropathology. Given the complexity of this disease, several aetiologies have been proposed. One of the theories includes variations in mitochondrial DNA (mtDNA) that affect the energy production in mitochondrial respiratory chain and consequently affect the tissue with higher energy demands, the central nervous system. The aim of our study is to identify variations of MT-CYB gene in 70 DNA samples of patients with probable diagnosis of FTLD. Total DNA of the samples was extracted from peripheral blood and MT-CYB gene was analysed and the sequence variations found were submitted to an in silico analysis. A total of 37 different sequence variations were identified in 44 patients (63%): 22 are synonymous, 2 are novel variations (m.15073C>T; m.15127C>T) that have not been reported to date in MITOMAP database and 15 are non-synonymous. The results of the in silico analysis suggested that 3 variations may be pathogenic: m.14927A>C affects protein function according to SIFT and the amino acid is conserved in all mammals; m.15164T>C is predicted to be deleterious by Provean, it is an alteration in a critical position and is totally conserved in all species studied, and m.15465T>C affects protein function according to Poly-Phen and SIFT and is highly conserved in mammals. Further investigation is important to clarify a possible relationship between mtDNA variations and pathophysiology of FTLD. However, our study represents a significant improvement in the complex field of dementia such like FTLD
Description: Trabalho final de mestrado integrado em Medicina (Genética), apresentado á Faculdade de Medicina da Universidade de Coimbra
URI: http://hdl.handle.net/10316/31098
Rights: openAccess
Appears in Collections:FMUC Medicina - Teses de Mestrado

Files in This Item:
File Description SizeFormat
Tese MSc MIM Mónica Gonçalves final MJ_RG_MG.pdf887.38 kBAdobe PDFView/Open
Show full item record

Page view(s) 5

946
checked on Sep 21, 2020

Download(s)

94
checked on Sep 21, 2020

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.