Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1782151547999748096 |
---|---|
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. |
format | Text |
id | pubmed-2266725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT frumkindan amplificationofmultiplegenomiclocifromsinglecellsisolatedbylasermicrodissectionoftissues AT wasserstromadam amplificationofmultiplegenomiclocifromsinglecellsisolatedbylasermicrodissectionoftissues AT itzkovitzshalev amplificationofmultiplegenomiclocifromsinglecellsisolatedbylasermicrodissectionoftissues AT harmelinalon amplificationofmultiplegenomiclocifromsinglecellsisolatedbylasermicrodissectionoftissues AT rechavigideon amplificationofmultiplegenomiclocifromsinglecellsisolatedbylasermicrodissectionoftissues AT shapiroehud amplificationofmultiplegenomiclocifromsinglecellsisolatedbylasermicrodissectionoftissues |