Genomewide gain-of-function genetic screen identifies functionally active genes in mouse embryonic stem cells

Moshe Pritsker, Nicole R. Ford, Harry T. Jenq, Ihor R. Lemischka

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Embryonic stem (ES) cells hold great promise for the future of medicine. To elucidate the molecular mechanisms that control ES cell self-renewal and differentiation, a comprehensive knowledge of the molecules involved in these processes is required. Here we describe an effective approach for genomewide identification of functionally active genes in ES cells. This approach combines genetic screens based on cDNA libraries with microarray detection methods to permit high-throughput functional analyses. We implement this strategy to identify genes whose overexpression can maintain phenotypic properties of undifferentiated mouse ES cells under differentiation-inducing conditions, specifically in the absence of leukemia inhibitory factor. The identified genes encode a variety of regulatory proteins whose function in ES cells was previously unknown. Moreover, our approach is capable of detecting genes whose overexpression promote differentiation or cell death. Overall, our studies establish a methodology for highly sensitive identification of genes that confer particular phenotypes on ES cells. © 2006 by The National Academy of Sciences of the USA.
    Original languageEnglish
    Pages (from-to)6946-6951
    Number of pages5
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume103
    Issue number18
    DOIs
    Publication statusPublished - 2 May 2006

    Keywords

    • cDNA library
    • Differentiation
    • Microarray
    • Phenotype
    • Self-renewal

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