Por favor, use este identificador para citar o enlazar este ítem:http://uvadoc.uva.es/handle/10324/13278
Título
Splicing functional analysis of DNA variants within the breast cancer type 2 susceptibility gene (BRCA2), and its effect on hereditary breast and ovarian cancaer (HBOC): A hybrid minigene approach
Director o Tutor
Año del Documento
2015
Titulación
Máster en Investigación Biomédica
Resumen
We aim to assess exon 17 splicing variants involvement in the genetic susceptibility to HBOC, by a bioinformatic analysis and mRNA functional assays through a hybrid minigene strategy. 1) To select the candidate variants of the functional analysis based on a bioinformatic prediction, using online databases as BIC and algorithms as the presented on the Human Splicing Finder Database (HSF).
2) To construct and validate a wild type minigene that contains the 14-20 exons of BRCA2 and can be used as a vector of the functional analysis.
3) To generate each of the selected BRCA2 variants within the minigene. 4) To perform a functional analysis of the variants (driven in eukaryote cells), in order to evaluate its effect on the mRNA splicing.
5) To characterize the new-generated splicing patterns.
6) To contribute to the understanding of the HBOC genetic predisposition spectrum.
Materias (normalizadas)
Mamas - Cáncer - Diagnóstico
Idioma
spa
Derechos
openAccess
Aparece en las colecciones
- Trabajos Fin de Máster UVa [6334]
Ficheros en el ítem
![Attribution-NonCommercial-NoDerivatives 4.0 International](/themes/Mirage2//images/creativecommons/cc-by-nc-nd.png)