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Publication Detail
Parallel RNAi screens across different cell lines identify generic and cell type-specific regulators of actin organization and cell morphology.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Journal Article
  • Authors:
    Liu T, Sims D, Baum B
  • Publication date:
    2009
  • Pagination:
    R26, ?
  • Journal:
    Genome Biol
  • Volume:
    10
  • Issue:
    3
  • Status:
    Published
  • Country:
    England
  • PII:
    gb-2009-10-3-r26
  • Language:
    eng
  • Keywords:
    Actins, Animals, Cell Line, Cell Shape, Cell Surface Extensions, Central Nervous System, Drosophila Proteins, Drosophila melanogaster, Gene Expression Profiling, Gene Expression Regulation, Genes, Insect, Genetic Testing, Hemocytes, Oligonucleotide Array Sequence Analysis, Organ Specificity, Phenotype, Protein-Serine-Threonine Kinases, RNA Interference
Abstract
BACKGROUND: In recent years RNAi screening has proven a powerful tool for dissecting gene functions in animal cells in culture. However, to date, most RNAi screens have been performed in a single cell line, and results then extrapolated across cell types and systems. RESULTS: Here, to dissect generic and cell type-specific mechanisms underlying cell morphology, we have performed identical kinome RNAi screens in six different Drosophila cell lines, derived from two distinct tissues of origin. This analysis identified a core set of kinases required for normal cell morphology in all lines tested, together with a number of kinases with cell type-specific functions. Most significantly, the screen identified a role for minibrain (mnb/DYRK1A), a kinase associated with Down's syndrome, in the regulation of actin-based protrusions in CNS-derived cell lines. This cell type-specific requirement was not due to the peculiarities in the morphology of CNS-derived cells and could not be attributed to differences in mnb expression. Instead, it likely reflects differences in gene expression that constitute the cell type-specific functional context in which mnb/DYRK1A acts. CONCLUSIONS: Using parallel RNAi screens and gene expression analyses across cell types we have identified generic and cell type-specific regulators of cell morphology, which include mnb/DYRK1A in the regulation of protrusion morphology in CNS-derived cell lines. This analysis reveals the importance of using different cell types to gain a thorough understanding of gene function across the genome and, in the case of kinases, the difficulties of using the differential gene expression to predict function.
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