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Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues

BACKGROUND: Whole genome amplification (WGA) and laser assisted micro-dissection represent two recently developed technologies that can greatly advance biological and medical research. WGA allows the analysis of multiple genomic loci from a single genome and has been performed on single cells from c...

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Autores principales: Frumkin, Dan, Wasserstrom, Adam, Itzkovitz, Shalev, Harmelin, Alon, Rechavi, Gideon, Shapiro, Ehud
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266725/
https://www.ncbi.nlm.nih.gov/pubmed/18284708
http://dx.doi.org/10.1186/1472-6750-8-17
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author Frumkin, Dan
Wasserstrom, Adam
Itzkovitz, Shalev
Harmelin, Alon
Rechavi, Gideon
Shapiro, Ehud
author_facet Frumkin, Dan
Wasserstrom, Adam
Itzkovitz, Shalev
Harmelin, Alon
Rechavi, Gideon
Shapiro, Ehud
author_sort Frumkin, Dan
collection PubMed
description BACKGROUND: Whole genome amplification (WGA) and laser assisted micro-dissection represent two recently developed technologies that can greatly advance biological and medical research. WGA allows the analysis of multiple genomic loci from a single genome and has been performed on single cells from cell suspensions and from enzymatically-digested tissues. Laser micro-dissection makes it possible to isolate specific single cells from heterogeneous tissues. RESULTS: Here we applied for the first time WGA on laser micro-dissected single cells from stained tissue sections, and developed a protocol for sequentially performing the two procedures. The combined procedure allows correlating the cell's genome with its natural morphology and precise anatomical position. From each cell we amplified 122 genomic and mitochondrial loci. In cells obtained from fresh tissue sections, 64.5% of alleles successfully amplified to ~700000 copies each, and mitochondrial DNA was amplified successfully in all cells. Multiplex PCR amplification and analysis of cells from pre-stored sections yielded significantly poorer results. Sequencing and capillary electrophoresis of WGA products allowed detection of slippage mutations in microsatellites (MS), and point mutations in P53. CONCLUSION: Comprehensive genomic analysis of single cells from stained tissue sections opens new research opportunities for cell lineage and depth analyses, genome-wide mutation surveys, and other single cell assays.
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spelling pubmed-22667252008-03-11 Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues Frumkin, Dan Wasserstrom, Adam Itzkovitz, Shalev Harmelin, Alon Rechavi, Gideon Shapiro, Ehud BMC Biotechnol Methodology Article BACKGROUND: Whole genome amplification (WGA) and laser assisted micro-dissection represent two recently developed technologies that can greatly advance biological and medical research. WGA allows the analysis of multiple genomic loci from a single genome and has been performed on single cells from cell suspensions and from enzymatically-digested tissues. Laser micro-dissection makes it possible to isolate specific single cells from heterogeneous tissues. RESULTS: Here we applied for the first time WGA on laser micro-dissected single cells from stained tissue sections, and developed a protocol for sequentially performing the two procedures. The combined procedure allows correlating the cell's genome with its natural morphology and precise anatomical position. From each cell we amplified 122 genomic and mitochondrial loci. In cells obtained from fresh tissue sections, 64.5% of alleles successfully amplified to ~700000 copies each, and mitochondrial DNA was amplified successfully in all cells. Multiplex PCR amplification and analysis of cells from pre-stored sections yielded significantly poorer results. Sequencing and capillary electrophoresis of WGA products allowed detection of slippage mutations in microsatellites (MS), and point mutations in P53. CONCLUSION: Comprehensive genomic analysis of single cells from stained tissue sections opens new research opportunities for cell lineage and depth analyses, genome-wide mutation surveys, and other single cell assays. BioMed Central 2008-02-20 /pmc/articles/PMC2266725/ /pubmed/18284708 http://dx.doi.org/10.1186/1472-6750-8-17 Text en Copyright © 2008 Frumkin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Frumkin, Dan
Wasserstrom, Adam
Itzkovitz, Shalev
Harmelin, Alon
Rechavi, Gideon
Shapiro, Ehud
Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
title Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
title_full Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
title_fullStr Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
title_full_unstemmed Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
title_short Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
title_sort amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266725/
https://www.ncbi.nlm.nih.gov/pubmed/18284708
http://dx.doi.org/10.1186/1472-6750-8-17
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