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Generation of a Synthetic Human Chromosome with Two Centromeric Domains for Advanced Epigenetic Engineering Studies
[Image: see text] It is generally accepted that chromatin containing the histone H3 variant CENP-A is an epigenetic mark maintaining centromere identity. However, the pathways leading to the formation and maintenance of centromere chromatin remain poorly characterized due to difficulties of analysis...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951608/ https://www.ncbi.nlm.nih.gov/pubmed/29565577 http://dx.doi.org/10.1021/acssynbio.8b00018 |
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author | Pesenti, Elisa Kouprina, Natalay Liskovykh, Mikhail Aurich-Costa, Joan Larionov, Vladimir Masumoto, Hiroshi Earnshaw, William C. Molina, Oscar |
author_facet | Pesenti, Elisa Kouprina, Natalay Liskovykh, Mikhail Aurich-Costa, Joan Larionov, Vladimir Masumoto, Hiroshi Earnshaw, William C. Molina, Oscar |
author_sort | Pesenti, Elisa |
collection | PubMed |
description | [Image: see text] It is generally accepted that chromatin containing the histone H3 variant CENP-A is an epigenetic mark maintaining centromere identity. However, the pathways leading to the formation and maintenance of centromere chromatin remain poorly characterized due to difficulties of analysis of centromeric repeats in native chromosomes. To address this problem, in our previous studies we generated a human artificial chromosome (HAC) whose centromere contains a synthetic alpha-satellite (alphoid) DNA array containing the tetracycline operator, the alphoid(tetO)-HAC. The presence of tetO sequences allows the specific targeting of the centromeric region in the HAC with different chromatin modifiers fused to the tetracycline repressor. The alphoid(tetO)-HAC has been extensively used to investigate protein interactions within the kinetochore and to define the epigenetic signature of centromeric chromatin to maintain a functional kinetochore. In this study, we developed a novel synthetic HAC containing two alphoid DNA arrays with different targeting sequences, tetO, lacO and gal4, the alphoid(hybrid)-HAC. This new HAC can be used for detailed epigenetic engineering studies because its kinetochore can be simultaneously or independently targeted by different chromatin modifiers and other fusion proteins. |
format | Online Article Text |
id | pubmed-5951608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59516082018-05-15 Generation of a Synthetic Human Chromosome with Two Centromeric Domains for Advanced Epigenetic Engineering Studies Pesenti, Elisa Kouprina, Natalay Liskovykh, Mikhail Aurich-Costa, Joan Larionov, Vladimir Masumoto, Hiroshi Earnshaw, William C. Molina, Oscar ACS Synth Biol [Image: see text] It is generally accepted that chromatin containing the histone H3 variant CENP-A is an epigenetic mark maintaining centromere identity. However, the pathways leading to the formation and maintenance of centromere chromatin remain poorly characterized due to difficulties of analysis of centromeric repeats in native chromosomes. To address this problem, in our previous studies we generated a human artificial chromosome (HAC) whose centromere contains a synthetic alpha-satellite (alphoid) DNA array containing the tetracycline operator, the alphoid(tetO)-HAC. The presence of tetO sequences allows the specific targeting of the centromeric region in the HAC with different chromatin modifiers fused to the tetracycline repressor. The alphoid(tetO)-HAC has been extensively used to investigate protein interactions within the kinetochore and to define the epigenetic signature of centromeric chromatin to maintain a functional kinetochore. In this study, we developed a novel synthetic HAC containing two alphoid DNA arrays with different targeting sequences, tetO, lacO and gal4, the alphoid(hybrid)-HAC. This new HAC can be used for detailed epigenetic engineering studies because its kinetochore can be simultaneously or independently targeted by different chromatin modifiers and other fusion proteins. American Chemical Society 2018-03-22 2018-04-20 /pmc/articles/PMC5951608/ /pubmed/29565577 http://dx.doi.org/10.1021/acssynbio.8b00018 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Pesenti, Elisa Kouprina, Natalay Liskovykh, Mikhail Aurich-Costa, Joan Larionov, Vladimir Masumoto, Hiroshi Earnshaw, William C. Molina, Oscar Generation of a Synthetic Human Chromosome with Two Centromeric Domains for Advanced Epigenetic Engineering Studies |
title | Generation of a Synthetic Human Chromosome with Two
Centromeric Domains for Advanced Epigenetic Engineering Studies |
title_full | Generation of a Synthetic Human Chromosome with Two
Centromeric Domains for Advanced Epigenetic Engineering Studies |
title_fullStr | Generation of a Synthetic Human Chromosome with Two
Centromeric Domains for Advanced Epigenetic Engineering Studies |
title_full_unstemmed | Generation of a Synthetic Human Chromosome with Two
Centromeric Domains for Advanced Epigenetic Engineering Studies |
title_short | Generation of a Synthetic Human Chromosome with Two
Centromeric Domains for Advanced Epigenetic Engineering Studies |
title_sort | generation of a synthetic human chromosome with two
centromeric domains for advanced epigenetic engineering studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951608/ https://www.ncbi.nlm.nih.gov/pubmed/29565577 http://dx.doi.org/10.1021/acssynbio.8b00018 |
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