Long non-coding RNA contributes to direct conversion reprogramming
| Autor(a) principal: | |
|---|---|
| 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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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 |
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info:eu-repo/semantics/masterThesis |
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masterThesis |
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publishedVersion |
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http://hdl.handle.net/10362/19464 |
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http://hdl.handle.net/10362/19464 |
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eng |
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eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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