Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies

Bibliographic Details
Main Author: Gouveia, Ana Maria Furtado
Publication Date: 2022
Format: Master thesis
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.22/21749
Summary: Herditary transthyretin-mediated amyloidosis (ATTRv) is a severe disease, dominat, autosomal amyloidois characterized by a progressive polyneuropathy, due to a point mutation in TTR gene, causing the deposition of amyloid fibrils in peripheric nerves. Due to wide variability in age-at-onset (AO), two main groups were stablished, early-onset (AO˂50 years) and late-onset (AO≥50 years). The main goal of this project was the analysis of RNA transcripts theta could act as modifiers of phenotypic variablility in ATTRv patient biopsies. Therefore, it was stablished wo main steps: (A) extraction and quantification of RNA from paraffin biopsies and (B) analysis of RNA transcripts that will allow to explain phenotypic variability in ATTRv. Five differentially expressed genes were identified in salivar gland samples. MGAM2 gene stood out between the other four genes due to its higher expression in the early AO group. This gene may be associated with the inhibition of a protectice factor that was not identified yet. Overall, our study may be a precursor to future exploration of proein-protein interactions, as well as the SNPs detection in differentially expressed genes that may modulate the phenotypic variability in ATTRv.
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spelling Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsiesHereditary transthyretin-mediated amyloidosisTransthyretinRNA transcriptsModifiers of phenotypic variabilityHerditary transthyretin-mediated amyloidosis (ATTRv) is a severe disease, dominat, autosomal amyloidois characterized by a progressive polyneuropathy, due to a point mutation in TTR gene, causing the deposition of amyloid fibrils in peripheric nerves. Due to wide variability in age-at-onset (AO), two main groups were stablished, early-onset (AO˂50 years) and late-onset (AO≥50 years). The main goal of this project was the analysis of RNA transcripts theta could act as modifiers of phenotypic variablility in ATTRv patient biopsies. Therefore, it was stablished wo main steps: (A) extraction and quantification of RNA from paraffin biopsies and (B) analysis of RNA transcripts that will allow to explain phenotypic variability in ATTRv. Five differentially expressed genes were identified in salivar gland samples. MGAM2 gene stood out between the other four genes due to its higher expression in the early AO group. This gene may be associated with the inhibition of a protectice factor that was not identified yet. Overall, our study may be a precursor to future exploration of proein-protein interactions, as well as the SNPs detection in differentially expressed genes that may modulate the phenotypic variability in ATTRv.Ferreira, Miguel AlvesCirnes, LuísGranja, SaraREPOSITÓRIO P.PORTOGouveia, Ana Maria Furtado2023-01-23T09:43:51Z2022-11-282022-11-28T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10400.22/21749urn:tid:203154258enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-07T10:29:01Zoai:recipp.ipp.pt:10400.22/21749Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T00:56:55.688940Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
title Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
spellingShingle Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
Gouveia, Ana Maria Furtado
Hereditary transthyretin-mediated amyloidosis
Transthyretin
RNA transcripts
Modifiers of phenotypic variability
title_short Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
title_full Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
title_fullStr Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
title_full_unstemmed Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
title_sort Transcripts as modifiers of phenotypic variability in hereditary transthyretin-mediated amyloidosis biopsies
author Gouveia, Ana Maria Furtado
author_facet Gouveia, Ana Maria Furtado
author_role author
dc.contributor.none.fl_str_mv Ferreira, Miguel Alves
Cirnes, Luís
Granja, Sara
REPOSITÓRIO P.PORTO
dc.contributor.author.fl_str_mv Gouveia, Ana Maria Furtado
dc.subject.por.fl_str_mv Hereditary transthyretin-mediated amyloidosis
Transthyretin
RNA transcripts
Modifiers of phenotypic variability
topic Hereditary transthyretin-mediated amyloidosis
Transthyretin
RNA transcripts
Modifiers of phenotypic variability
description Herditary transthyretin-mediated amyloidosis (ATTRv) is a severe disease, dominat, autosomal amyloidois characterized by a progressive polyneuropathy, due to a point mutation in TTR gene, causing the deposition of amyloid fibrils in peripheric nerves. Due to wide variability in age-at-onset (AO), two main groups were stablished, early-onset (AO˂50 years) and late-onset (AO≥50 years). The main goal of this project was the analysis of RNA transcripts theta could act as modifiers of phenotypic variablility in ATTRv patient biopsies. Therefore, it was stablished wo main steps: (A) extraction and quantification of RNA from paraffin biopsies and (B) analysis of RNA transcripts that will allow to explain phenotypic variability in ATTRv. Five differentially expressed genes were identified in salivar gland samples. MGAM2 gene stood out between the other four genes due to its higher expression in the early AO group. This gene may be associated with the inhibition of a protectice factor that was not identified yet. Overall, our study may be a precursor to future exploration of proein-protein interactions, as well as the SNPs detection in differentially expressed genes that may modulate the phenotypic variability in ATTRv.
publishDate 2022
dc.date.none.fl_str_mv 2022-11-28
2022-11-28T00:00:00Z
2023-01-23T09:43:51Z
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