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  A genome-wide resource for the analysis of protein localisation in Drosophila.

Sarov, M., Barz, C., Jambor, H., Hein, M. Y., Schmied, C., Suchold, D., et al. (2016). A genome-wide resource for the analysis of protein localisation in Drosophila. eLife, 5: e12068.

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Sarov, Mihail1, Author           
Barz, Christiane, Author
Jambor, Helena1, Author           
Hein, Marco Y, Author
Schmied, Christopher2, Author           
Suchold, Dana3, Author
Stender, Bettina, Author
Janosch, Stephan1, Author           
Kj, Vinay Vikas, Author
Krishnan, R T, Author
Krishnamoorthy, Aishwarya, Author
Ferreira, Irene R S, Author
Ejsmont, Radoslaw K2, Author           
Finkl, Katja, Author
Hasse, Susanne1, Author           
Kämpfer, Philipp, Author
Plewka, Nicole, Author
Vinis, Elisabeth2, Author           
Schloissnig, Siegfried, Author
Knust, Elisabeth1, Author           
Hartenstein, Volker2, Author           Mann, Matthias, AuthorRamaswami, Mani, AuthorVijayRaghavan, K, AuthorTomancak, Pavel1, Author           Schnorrer, Frank3, Author more..
Affiliations:
1Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              
2External Organizations, ou_persistent22              
3Max Planck Society, ou_persistent13              

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 Abstract: The Drosophila genome contains >13,000 protein coding genes, the majority of which remain poorly investigated. Important reasons include the lack of antibodies or reporter constructs to visualise these proteins. Here we present a genome-wide fosmid library of 10,000 GFP-tagged clones, comprising tagged genes and most of their regulatory information. For 880 tagged proteins we created transgenic lines and for a total of 207 lines we assessed protein expression and localisation in ovaries, embryos, pupae or adults by stainings and live imaging approaches. Importantly, we visualised many proteins at endogenous expression levels and found a large fraction of them localising to subcellular compartments. By applying genetic complementation tests we estimate that about two-thirds of the tagged proteins are functional. Moreover, these tagged proteins enable interaction proteomics from developing pupae and adult flies. Taken together, this resource will boost systematic analysis of protein expression and localisation in various cellular and developmental contexts.

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 Dates: 2016
 Publication Status: Issued
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 Identifiers: eDoc: 732390
Other: 6441
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Title: eLife
Source Genre: Journal
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Pages: - Volume / Issue: 5 Sequence Number: e12068 Start / End Page: - Identifier: -