Projects per year
Abstract / Description of output
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 alphoidtetO-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 alphoidtetO-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 alphoidhybrid-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.
Original language | English |
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Pages (from-to) | 1116-1130 |
Number of pages | 15 |
Journal | ACS Synthetic Biology |
Volume | 7 |
Issue number | 4 |
Early online date | 22 Mar 2018 |
DOIs | |
Publication status | Published - 20 Apr 2018 |
Keywords / Materials (for Non-textual outputs)
- centromere
- chromosome segregation
- human artificial chromosome
- kinetochore
- mitosis
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Dive into the research topics of 'Generation of a Synthetic Human Chromosome with Two Centromeric Domains for Advanced Epigenetic Engineering Studies'. Together they form a unique fingerprint.Projects
- 2 Finished
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SynthSys-Mammalian: Edinburgh Mammalian Synthetic Biology Research Centre
Rosser, S., Bird, A., Cai, Y., Earnshaw, B., Millar, A., Molina, N., Pilizota, T., Swain, P. & Waites, W.
14/11/14 → 31/03/22
Project: Research
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The role of non-histone proteins in chromosome structure and function during mitosis
1/01/11 → 30/09/16
Project: Research