TY - JOUR
T1 - Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissues
AU - Frumkin, Dan
AU - Wasserstrom, Adam
AU - Itzkovitz, Shalev
AU - Harmelin, Alon
AU - Rechavi, Gideon
AU - Shapiro, Ehud
N1 - Funding Information:
The work was supported by Kahn Family Foundation, by The Israel Academy of Science and Humanities (Bikura), by The Yeshaya Horowitz association through the center for Complexity Science, by The Research Grant from Dr. Mordecai Roshwald, by The Grant from Kenneth and Sally Leaf-man Appelbaum Discovery Fund, by The Estate of Karl Felix Jakubskind and by The Clore Center for Biological Physics. Ehud Shapiro is the Incumbent of The Harry Weinrebe Professorial Chair of Computer Science and Biology and of The France Telecom – Orange Excellence Chair for Interdisciplinary Studies of the Paris "Centre de Recherche Interdisciplinaire" (FTO/ CRI). Flight Attendants Medical Research Institute (FAMRI). G.R. holds the Djerassi Chair in Oncology at the Sackler Faculty of Medicine, Tel-Aviv University.
PY - 2008/2/20
Y1 - 2008/2/20
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=40549127780&partnerID=8YFLogxK
U2 - 10.1186/1472-6750-8-17
DO - 10.1186/1472-6750-8-17
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AN - SCOPUS:40549127780
SN - 1472-6750
VL - 8
JO - BMC Biotechnology
JF - BMC Biotechnology
M1 - 17
ER -