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  Genome-scale RNAi profiling of cell division in human tissue culture cells

Kittler, R., Pelletier, L., Heninger, A. K., Slabicki, M., Theis, M., Miroslaw, L., et al. (2007). Genome-scale RNAi profiling of cell division in human tissue culture cells. Nat Cell Biol, 9(12), 1401-12. doi:10.1038/ncb1659.

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Kittler, R., Author
Pelletier, L., Author
Heninger, A. K., Author
Slabicki, M., Author
Theis, M., Author
Miroslaw, L., Author
Poser, I., Author
Lawo, S.1, Author           
Grabner, H., Author
Kozak, K., Author
Wagner, J., Author
Surendranath, V., Author
Richter, C., Author
Bowen, W., Author
Jackson, A. L., Author
Habermann, B., Author
Hyman, A. A., Author
Buchholz, F., Author
Affiliations:
1CRISPR Screening, Core Facilities, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3394014              

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Free keywords: Cell Division/*physiology Gene Expression Profiling *Genome, Human HeLa Cells Humans *RNA Interference RNA, Small Interfering/metabolism
 Abstract: Cell division is fundamental for all organisms. Here we report a genome-scale RNA-mediated interference screen in HeLa cells designed to identify human genes that are important for cell division. We have used a library of endoribonuclease-prepared short interfering RNAs for gene silencing and have used DNA content analysis to identify genes that induced cell cycle arrest or altered ploidy on silencing. Validation and secondary assays were performed to generate a nine-parameter loss-of-function phenoprint for each of the genes. These phenotypic signatures allowed the assignment of genes to specific functional classes by combining hierarchical clustering, cross-species analysis and proteomic data mining. We highlight the richness of our dataset by ascribing novel functions to genes in mitosis and cytokinesis. In particular, we identify two evolutionarily conserved transcriptional regulatory networks that govern cytokinesis. Our work provides an experimental framework from which the systematic analysis of novel genes necessary for cell division in human cells can begin.

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 Dates: 2007-122007-11-13
 Publication Status: Issued
 Pages: -
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 Identifiers: Other: 17994010
DOI: 10.1038/ncb1659
ISSN: 1465-7392 (Print)1465-7392 (Linking)
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Title: Nat Cell Biol
Source Genre: Journal
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Pages: - Volume / Issue: 9 (12) Sequence Number: - Start / End Page: 1401 - 12 Identifier: -