Publication Date:
2002-08-06
Description:
A key goal of biology is to relate the expression of specific genes to a particular cellular phenotype. However, current assays for gene expression destroy the structural context. By combining advances in computational fluorescence microscopy with multiplex probe design, we devised technology in which the expression of many genes can be visualized simultaneously inside single cells with high spatial and temporal resolution. Analysis of 11 genes in serum-stimulated cultured cells revealed unique patterns of gene expression within individual cells. Using the nucleus as the substrate for parallel gene analysis, we provide a platform for the fusion of genomics and cell biology: "cellular genomics."〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levsky, Jeffrey M -- Shenoy, Shailesh M -- Pezo, Rossanna C -- Singer, Robert H -- GM54887/GM/NIGMS NIH HHS/ -- R33CA83208/CA/NCI NIH HHS/ -- T32GM07288/GM/NIGMS NIH HHS/ -- T32GM07491/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2002 Aug 2;297(5582):836-40.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12161654" target="_blank"〉PubMed〈/a〉
Keywords:
Adenocarcinoma/genetics
;
Cell Nucleus/genetics
;
Cells/*cytology/*metabolism
;
Colonic Neoplasms/genetics
;
Color
;
DNA Probes
;
Fibroblasts
;
Gene Expression Profiling/instrumentation/*methods
;
*Gene Expression Regulation
;
Genes
;
Genomics/instrumentation/methods
;
Humans
;
Microscopy, Fluorescence/instrumentation/*methods
;
Odds Ratio
;
RNA/genetics/metabolism
;
Sensitivity and Specificity
;
Time Factors
;
Transcription, Genetic
;
Tumor Cells, Cultured
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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