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PMID: 19879847 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Analysis of cell fate from single-cell gene expression profiles in C. elegans.

Cell ·Vol. 139 ·No. 3 ·2009-10-30 ·Pages 623-33

Liu X, Long F, Peng H, Aerni SJ, Jiang M, Sánchez-Blanco A, Murray JI, Preston E, Mericle B, Batzoglou S, Myers EW, Kim SK

Abstract

The C. elegans cell lineage provides a unique opportunity to look at how cell lineage affects patterns of gene expression. We developed an automatic cell lineage analyzer that converts high-resolution images of worms into a data table showing fluorescence expression with single-cell resolution. We generated expression profiles of 93 genes in 363 specific cells from L1 stage larvae and found that cells with identical fates can be formed by different gene regulatory pathways. Molecular signatures identified repeating cell fate modules within the cell lineage and enabled the generation of a molecular differentiation map that reveals points in the cell lineage when developmental fates of daughter cells begin to diverge. These results demonstrate insights that become possible using computational approaches to analyze quantitative expression from many genes in parallel using a digital gene expression atlas.

MeSH Terms
Animals Caenorhabditis elegans/cytology,genetics,metabolism Caenorhabditis elegans Proteins Cell Differentiation Cell Lineage Gene Expression Profiling/methods
Chemicals
Caenorhabditis elegans Proteins
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Liu Xiao
Department of Developmental Biology, Stanford University Medical Center, Stanford, CA 94305, USA.
Long Fuhui
Peng Hanchuan
Aerni Sarah J
Jiang Min
Sánchez-Blanco Adolfo
Murray John I
Preston Elicia
Mericle Barbara
Batzoglou Serafim
Myers Eugene W
Kim Stuart K
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Article Info
Journal
Cell
Abbr.
Cell
ISSN
1097-4172
Published
2009-10-30
Pages
623-33
Language
English
Region
United States
NLM ID
0413066
PMCID
PMC4709123
Subset
IM
Grants
NIA NIH HHS · R01 AG025941 · United States
Howard Hughes Medical Institute · United States
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