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Transcription Factor Analysis in Trypanosomatids

Known transcription factors of trypanosomatid organisms are extremely divergent in amino acid sequence to their counterparts in other eukaryotes. Sequence similarity is so limited that factors have been primarily identified by functional and structural studies. In addition, trypanosomatids may have...

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Autores principales: Günzl, Arthur, Srivastava, Ankita, Gosavi, Ujwala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337167/
https://www.ncbi.nlm.nih.gov/pubmed/32221925
http://dx.doi.org/10.1007/978-1-0716-0294-2_16
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author Günzl, Arthur
Srivastava, Ankita
Gosavi, Ujwala
author_facet Günzl, Arthur
Srivastava, Ankita
Gosavi, Ujwala
author_sort Günzl, Arthur
collection PubMed
description Known transcription factors of trypanosomatid organisms are extremely divergent in amino acid sequence to their counterparts in other eukaryotes. Sequence similarity is so limited that factors have been primarily identified by functional and structural studies. In addition, trypanosomatids may have evolved factors that are specific to this group of organisms. Under these circumstances, an in vitro transcription system is invaluable as it allows for unambiguous determination of a factor’s transcriptional role. Here we describe procedures for the preparation of transcriptionally active extracts, detail in vitro transcription reactions, and specify the particular strategy necessary to detect template-derived RNA in this system. As examples of how to use this system, we describe factor depletion from extract and antibody-mediated interference with a factor’s transcriptional function. Furthermore, we detail a promoter pull-down assay that makes use of the extracts and facilitates analysis of a factor’s interaction with promoter DNA.
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spelling pubmed-73371672020-07-06 Transcription Factor Analysis in Trypanosomatids Günzl, Arthur Srivastava, Ankita Gosavi, Ujwala Methods Mol Biol Article Known transcription factors of trypanosomatid organisms are extremely divergent in amino acid sequence to their counterparts in other eukaryotes. Sequence similarity is so limited that factors have been primarily identified by functional and structural studies. In addition, trypanosomatids may have evolved factors that are specific to this group of organisms. Under these circumstances, an in vitro transcription system is invaluable as it allows for unambiguous determination of a factor’s transcriptional role. Here we describe procedures for the preparation of transcriptionally active extracts, detail in vitro transcription reactions, and specify the particular strategy necessary to detect template-derived RNA in this system. As examples of how to use this system, we describe factor depletion from extract and antibody-mediated interference with a factor’s transcriptional function. Furthermore, we detail a promoter pull-down assay that makes use of the extracts and facilitates analysis of a factor’s interaction with promoter DNA. 2020 /pmc/articles/PMC7337167/ /pubmed/32221925 http://dx.doi.org/10.1007/978-1-0716-0294-2_16 Text en Open Access This chapter is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence and indicate if changes were made.
spellingShingle Article
Günzl, Arthur
Srivastava, Ankita
Gosavi, Ujwala
Transcription Factor Analysis in Trypanosomatids
title Transcription Factor Analysis in Trypanosomatids
title_full Transcription Factor Analysis in Trypanosomatids
title_fullStr Transcription Factor Analysis in Trypanosomatids
title_full_unstemmed Transcription Factor Analysis in Trypanosomatids
title_short Transcription Factor Analysis in Trypanosomatids
title_sort transcription factor analysis in trypanosomatids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337167/
https://www.ncbi.nlm.nih.gov/pubmed/32221925
http://dx.doi.org/10.1007/978-1-0716-0294-2_16
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