Cargando…
In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation
The chick embryo chorioallantoic membrane (CAM) represents a powerful in vivo model to study several physiological and pathological processes including inflammation and tumor progression. Nevertheless, the possibility of deepening the molecular processes in the CAM system is biased by the absence/sc...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720131/ https://www.ncbi.nlm.nih.gov/pubmed/33233345 http://dx.doi.org/10.3390/mps3040080 |
_version_ | 1783619804095053824 |
---|---|
author | Corsini, Michela Moroni, Emanuela Ravelli, Cosetta Grillo, Elisabetta Presta, Marco Mitola, Stefania |
author_facet | Corsini, Michela Moroni, Emanuela Ravelli, Cosetta Grillo, Elisabetta Presta, Marco Mitola, Stefania |
author_sort | Corsini, Michela |
collection | PubMed |
description | The chick embryo chorioallantoic membrane (CAM) represents a powerful in vivo model to study several physiological and pathological processes including inflammation and tumor progression. Nevertheless, the possibility of deepening the molecular processes in the CAM system is biased by the absence/scarcity of chemical and biological reagents, designed explicitly for avian species. This is particularly true for transcriptional factors, proteinaceous molecules that regulate various cellular responses, including proliferation, survival, and differentiation. Here, we propose a detailed antibody-independent protocol to visualize the activation and nuclear translocation of transcriptional factors in cells or in tissues of different animal species. As a proof of concept, DNA/cAMP response element-binding protein (CREB) interaction was characterized on the CAM tissue using oligonucleotides containing the palindromic binding sequence of CREB. Scrambled oligonucleotides were used as controls. In situ DNA/protein interaction protocol is a versatile method that is useful for the study of transcription factors in the cell and tissue of different origins. |
format | Online Article Text |
id | pubmed-7720131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77201312020-12-08 In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation Corsini, Michela Moroni, Emanuela Ravelli, Cosetta Grillo, Elisabetta Presta, Marco Mitola, Stefania Methods Protoc Protocol The chick embryo chorioallantoic membrane (CAM) represents a powerful in vivo model to study several physiological and pathological processes including inflammation and tumor progression. Nevertheless, the possibility of deepening the molecular processes in the CAM system is biased by the absence/scarcity of chemical and biological reagents, designed explicitly for avian species. This is particularly true for transcriptional factors, proteinaceous molecules that regulate various cellular responses, including proliferation, survival, and differentiation. Here, we propose a detailed antibody-independent protocol to visualize the activation and nuclear translocation of transcriptional factors in cells or in tissues of different animal species. As a proof of concept, DNA/cAMP response element-binding protein (CREB) interaction was characterized on the CAM tissue using oligonucleotides containing the palindromic binding sequence of CREB. Scrambled oligonucleotides were used as controls. In situ DNA/protein interaction protocol is a versatile method that is useful for the study of transcription factors in the cell and tissue of different origins. MDPI 2020-11-21 /pmc/articles/PMC7720131/ /pubmed/33233345 http://dx.doi.org/10.3390/mps3040080 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Corsini, Michela Moroni, Emanuela Ravelli, Cosetta Grillo, Elisabetta Presta, Marco Mitola, Stefania In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation |
title | In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation |
title_full | In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation |
title_fullStr | In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation |
title_full_unstemmed | In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation |
title_short | In Situ DNA/Protein Interaction Assay to Visualize Transcriptional Factor Activation |
title_sort | in situ dna/protein interaction assay to visualize transcriptional factor activation |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720131/ https://www.ncbi.nlm.nih.gov/pubmed/33233345 http://dx.doi.org/10.3390/mps3040080 |
work_keys_str_mv | AT corsinimichela insitudnaproteininteractionassaytovisualizetranscriptionalfactoractivation AT moroniemanuela insitudnaproteininteractionassaytovisualizetranscriptionalfactoractivation AT ravellicosetta insitudnaproteininteractionassaytovisualizetranscriptionalfactoractivation AT grilloelisabetta insitudnaproteininteractionassaytovisualizetranscriptionalfactoractivation AT prestamarco insitudnaproteininteractionassaytovisualizetranscriptionalfactoractivation AT mitolastefania insitudnaproteininteractionassaytovisualizetranscriptionalfactoractivation |