Long non-coding RNA contributes to direct conversion reprogramming

Detalhes bibliográficos
Autor(a) principal: Franco, António Duarte Zapico Bicho de Sousa
Data de Publicação: 2016
Tipo de documento: Dissertação
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10362/19464
Resumo: Over the last years, research led lncRNAs to go from transcriptional noise to important regulators of gene expression, being now known their association with many regulatory pathways by a wide set of mechanisms. Some of these RNAs play very important roles in cell differentiation, given their differential and temporal expression during tissue and organismal development. The discovery that terminally differentiated cells could revert to pluripotency or be redirected to multipotent progenitors of different lineages through forced expression of a specific onset of genes opened the way for direct conversion studies. The fact that various lncRNAs have been associated with differentiation, pluripotency and cancer indicates that these molecules might be useful tools in direct conversion. Manipulation of lncRNA expression during cell reprogramming could provide aid in overcoming current protocol limitations as the tumorigenic potential of iPSCs, low efficiencies and aging related epigenetic resistance. LncRNAs with influence in cell character transitions such as epithelial-mesenchymal transition (EMT) or mesenchymal-epithelial transition (MET) could contribute to direct conversion reprograming, as could lncRNAs that are specifically expressed in the reprogramming target cell line. We herein present two lncRNAs with the mentioned characteristics, Zeb2NAT and Pnky, respectively, as potential targets for improving fibroblast direct conversion reprogramming to multipotent hematopoietic and neural progenitors with a single pluripotency transcription factor (TF). Downregulation of Zeb2Nat during direct conversion seems to impair reprogramming efficiency, however if upregulating this lncRNA will have an improving effect is still under study. Getting unlimited patient-specific progenitor cells of different lineages from more accessible sources presents an enormous medical issue.
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spelling Long non-coding RNA contributes to direct conversion reprogrammingLncRNADirect reprogrammingMultipotencyZeb2NATPnkyDomínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e TecnologiasOver the last years, research led lncRNAs to go from transcriptional noise to important regulators of gene expression, being now known their association with many regulatory pathways by a wide set of mechanisms. Some of these RNAs play very important roles in cell differentiation, given their differential and temporal expression during tissue and organismal development. The discovery that terminally differentiated cells could revert to pluripotency or be redirected to multipotent progenitors of different lineages through forced expression of a specific onset of genes opened the way for direct conversion studies. The fact that various lncRNAs have been associated with differentiation, pluripotency and cancer indicates that these molecules might be useful tools in direct conversion. Manipulation of lncRNA expression during cell reprogramming could provide aid in overcoming current protocol limitations as the tumorigenic potential of iPSCs, low efficiencies and aging related epigenetic resistance. LncRNAs with influence in cell character transitions such as epithelial-mesenchymal transition (EMT) or mesenchymal-epithelial transition (MET) could contribute to direct conversion reprograming, as could lncRNAs that are specifically expressed in the reprogramming target cell line. We herein present two lncRNAs with the mentioned characteristics, Zeb2NAT and Pnky, respectively, as potential targets for improving fibroblast direct conversion reprogramming to multipotent hematopoietic and neural progenitors with a single pluripotency transcription factor (TF). Downregulation of Zeb2Nat during direct conversion seems to impair reprogramming efficiency, however if upregulating this lncRNA will have an improving effect is still under study. Getting unlimited patient-specific progenitor cells of different lineages from more accessible sources presents an enormous medical issue.Jesus, BrunoFonseca, Maria do CarmoRUNFranco, António Duarte Zapico Bicho de Sousa2016-11-25T15:45:29Z2016-092016-112016-09-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10362/19464enginfo: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:RCAAP2024-05-22T17:24:02Zoai:run.unl.pt:10362/19464Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T16:55:03.649635Repositórios 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 Long non-coding RNA contributes to direct conversion reprogramming
title Long non-coding RNA contributes to direct conversion reprogramming
spellingShingle Long non-coding RNA contributes to direct conversion reprogramming
Franco, António Duarte Zapico Bicho de Sousa
LncRNA
Direct reprogramming
Multipotency
Zeb2NAT
Pnky
Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias
title_short Long non-coding RNA contributes to direct conversion reprogramming
title_full Long non-coding RNA contributes to direct conversion reprogramming
title_fullStr Long non-coding RNA contributes to direct conversion reprogramming
title_full_unstemmed Long non-coding RNA contributes to direct conversion reprogramming
title_sort Long non-coding RNA contributes to direct conversion reprogramming
author Franco, António Duarte Zapico Bicho de Sousa
author_facet Franco, António Duarte Zapico Bicho de Sousa
author_role author
dc.contributor.none.fl_str_mv Jesus, Bruno
Fonseca, Maria do Carmo
RUN
dc.contributor.author.fl_str_mv Franco, António Duarte Zapico Bicho de Sousa
dc.subject.por.fl_str_mv LncRNA
Direct reprogramming
Multipotency
Zeb2NAT
Pnky
Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias
topic LncRNA
Direct reprogramming
Multipotency
Zeb2NAT
Pnky
Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias
description Over the last years, research led lncRNAs to go from transcriptional noise to important regulators of gene expression, being now known their association with many regulatory pathways by a wide set of mechanisms. Some of these RNAs play very important roles in cell differentiation, given their differential and temporal expression during tissue and organismal development. The discovery that terminally differentiated cells could revert to pluripotency or be redirected to multipotent progenitors of different lineages through forced expression of a specific onset of genes opened the way for direct conversion studies. The fact that various lncRNAs have been associated with differentiation, pluripotency and cancer indicates that these molecules might be useful tools in direct conversion. Manipulation of lncRNA expression during cell reprogramming could provide aid in overcoming current protocol limitations as the tumorigenic potential of iPSCs, low efficiencies and aging related epigenetic resistance. LncRNAs with influence in cell character transitions such as epithelial-mesenchymal transition (EMT) or mesenchymal-epithelial transition (MET) could contribute to direct conversion reprograming, as could lncRNAs that are specifically expressed in the reprogramming target cell line. We herein present two lncRNAs with the mentioned characteristics, Zeb2NAT and Pnky, respectively, as potential targets for improving fibroblast direct conversion reprogramming to multipotent hematopoietic and neural progenitors with a single pluripotency transcription factor (TF). Downregulation of Zeb2Nat during direct conversion seems to impair reprogramming efficiency, however if upregulating this lncRNA will have an improving effect is still under study. Getting unlimited patient-specific progenitor cells of different lineages from more accessible sources presents an enormous medical issue.
publishDate 2016
dc.date.none.fl_str_mv 2016-11-25T15:45:29Z
2016-09
2016-11
2016-09-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
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url http://hdl.handle.net/10362/19464
dc.language.iso.fl_str_mv eng
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dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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