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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...

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Autores principales: Pesenti, Elisa, Kouprina, Natalay, Liskovykh, Mikhail, Aurich-Costa, Joan, Larionov, Vladimir, Masumoto, Hiroshi, Earnshaw, William C., Molina, Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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