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Efficient assembly of de novo human artificial chromosomes from large genomic loci
BACKGROUND: Human Artificial Chromosomes (HACs) are potentially useful vectors for gene transfer studies and for functional annotation of the genome because of their suitability for cloning, manipulating and transferring large segments of the genome. However, development of HACs for the transfer of...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182356/ https://www.ncbi.nlm.nih.gov/pubmed/15998466 http://dx.doi.org/10.1186/1472-6750-5-21 |
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author | Basu, Joydeep Compitello, George Stromberg, Gregory Willard, Huntington F Van Bokkelen, Gil |
author_facet | Basu, Joydeep Compitello, George Stromberg, Gregory Willard, Huntington F Van Bokkelen, Gil |
author_sort | Basu, Joydeep |
collection | PubMed |
description | BACKGROUND: Human Artificial Chromosomes (HACs) are potentially useful vectors for gene transfer studies and for functional annotation of the genome because of their suitability for cloning, manipulating and transferring large segments of the genome. However, development of HACs for the transfer of large genomic loci into mammalian cells has been limited by difficulties in manipulating high-molecular weight DNA, as well as by the low overall frequencies of de novo HAC formation. Indeed, to date, only a small number of large (>100 kb) genomic loci have been reported to be successfully packaged into de novo HACs. RESULTS: We have developed novel methodologies to enable efficient assembly of HAC vectors containing any genomic locus of interest. We report here the creation of a novel, bimolecular system based on bacterial artificial chromosomes (BACs) for the construction of HACs incorporating any defined genomic region. We have utilized this vector system to rapidly design, construct and validate multiple de novo HACs containing large (100–200 kb) genomic loci including therapeutically significant genes for human growth hormone (HGH), polycystic kidney disease (PKD1) and ß-globin. We report significant differences in the ability of different genomic loci to support de novo HAC formation, suggesting possible effects of cis-acting genomic elements. Finally, as a proof of principle, we have observed sustained ß-globin gene expression from HACs incorporating the entire 200 kb ß-globin genomic locus for over 90 days in the absence of selection. CONCLUSION: Taken together, these results are significant for the development of HAC vector technology, as they enable high-throughput assembly and functional validation of HACs containing any large genomic locus. We have evaluated the impact of different genomic loci on the frequency of HAC formation and identified segments of genomic DNA that appear to facilitate de novo HAC formation. These genomic loci may be useful for identifying discrete functional elements that may be incorporated into future generations of HAC vectors. |
format | Text |
id | pubmed-1182356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11823562005-08-04 Efficient assembly of de novo human artificial chromosomes from large genomic loci Basu, Joydeep Compitello, George Stromberg, Gregory Willard, Huntington F Van Bokkelen, Gil BMC Biotechnol Research Article BACKGROUND: Human Artificial Chromosomes (HACs) are potentially useful vectors for gene transfer studies and for functional annotation of the genome because of their suitability for cloning, manipulating and transferring large segments of the genome. However, development of HACs for the transfer of large genomic loci into mammalian cells has been limited by difficulties in manipulating high-molecular weight DNA, as well as by the low overall frequencies of de novo HAC formation. Indeed, to date, only a small number of large (>100 kb) genomic loci have been reported to be successfully packaged into de novo HACs. RESULTS: We have developed novel methodologies to enable efficient assembly of HAC vectors containing any genomic locus of interest. We report here the creation of a novel, bimolecular system based on bacterial artificial chromosomes (BACs) for the construction of HACs incorporating any defined genomic region. We have utilized this vector system to rapidly design, construct and validate multiple de novo HACs containing large (100–200 kb) genomic loci including therapeutically significant genes for human growth hormone (HGH), polycystic kidney disease (PKD1) and ß-globin. We report significant differences in the ability of different genomic loci to support de novo HAC formation, suggesting possible effects of cis-acting genomic elements. Finally, as a proof of principle, we have observed sustained ß-globin gene expression from HACs incorporating the entire 200 kb ß-globin genomic locus for over 90 days in the absence of selection. CONCLUSION: Taken together, these results are significant for the development of HAC vector technology, as they enable high-throughput assembly and functional validation of HACs containing any large genomic locus. We have evaluated the impact of different genomic loci on the frequency of HAC formation and identified segments of genomic DNA that appear to facilitate de novo HAC formation. These genomic loci may be useful for identifying discrete functional elements that may be incorporated into future generations of HAC vectors. BioMed Central 2005-07-05 /pmc/articles/PMC1182356/ /pubmed/15998466 http://dx.doi.org/10.1186/1472-6750-5-21 Text en Copyright © 2005 Basu et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Basu, Joydeep Compitello, George Stromberg, Gregory Willard, Huntington F Van Bokkelen, Gil Efficient assembly of de novo human artificial chromosomes from large genomic loci |
title | Efficient assembly of de novo human artificial chromosomes from large genomic loci |
title_full | Efficient assembly of de novo human artificial chromosomes from large genomic loci |
title_fullStr | Efficient assembly of de novo human artificial chromosomes from large genomic loci |
title_full_unstemmed | Efficient assembly of de novo human artificial chromosomes from large genomic loci |
title_short | Efficient assembly of de novo human artificial chromosomes from large genomic loci |
title_sort | efficient assembly of de novo human artificial chromosomes from large genomic loci |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182356/ https://www.ncbi.nlm.nih.gov/pubmed/15998466 http://dx.doi.org/10.1186/1472-6750-5-21 |
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