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Functional genomics reveals genes involved in protein secretion and Golgi organization

Abstract

Yeast genetics and in vitro biochemical analysis have identified numerous genes involved in protein secretion1,2. As compared with yeast, however, the metazoan secretory pathway is more complex and many mechanisms that regulate organization of the Golgi apparatus remain poorly characterized. We performed a genome-wide RNA-mediated interference screen in a Drosophila cell line to identify genes required for constitutive protein secretion. We then classified the genes on the basis of the effect of their depletion on organization of the Golgi membranes. Here we show that depletion of class A genes redistributes Golgi membranes into the endoplasmic reticulum, depletion of class B genes leads to Golgi fragmentation, depletion of class C genes leads to aggregation of Golgi membranes, and depletion of class D genes causes no obvious change. Of the 20 new gene products characterized so far, several localize to the Golgi membranes and the endoplasmic reticulum.

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Figure 1: HRP secretion in Drosophila S2 cells.
Figure 2: Identification of the genes involved in HRP secretion.
Figure 3: Drosophila genes involved in Golgi organization.
Figure 4: Localization of the products of new genes regulating secretion.

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References

  1. Novick, P. & Schekman, R. Secretion and cell-surface growth are blocked in a temperature-sensitive mutant of Saccharomyces cerevisiae. Proc. Natl Acad. Sci. USA 76, 1858–1862 (1979)

    Article  CAS  ADS  Google Scholar 

  2. Rothman, J. E. Mechanisms of intracellular protein transport. Nature 372, 55–63 (1994)

    Article  CAS  ADS  Google Scholar 

  3. Nichols, B. J. & Pelham, H. R. SNAREs and membrane fusion in the Golgi apparatus. Biochim. Biophys. Acta 1404, 9–31 (1998)

    Article  CAS  Google Scholar 

  4. Duden, R., Allan, V. & Kreis, T. Involvement of β-COP in membrane traffic through the Golgi complex. Trends Cell Biol. 1, 14–19 (1991)

    Article  CAS  Google Scholar 

  5. Serafini, T. et al. A coat subunit of Golgi-derived non-clathrin-coated vesicles with homology to the clathrin-coated vesicle coat protein β-adaptin. Nature 349, 215–220 (1991)

    Article  CAS  ADS  Google Scholar 

  6. Boutros, M. et al. Genome-wide RNAi analysis of growth and viability in Drosophila cells. Science 303, 832–835 (2004)

    Article  CAS  ADS  Google Scholar 

  7. DasGupta, R., Kaykas, A., Moon, R. T. & Perrimon, N. Functional genomic analysis of the Wnt-wingless signalling pathway. Science 308, 826–833 (2005)

    Article  CAS  ADS  Google Scholar 

  8. Eggert, U. S. et al. Parallel chemical genetic and genome-wide RNAi screens identify cytokinesis inhibitors and targets. PLoS Biol. 2, e379 (2004)

    Article  Google Scholar 

  9. Kiger, A. A. et al. A functional genomic analysis of cell morphology using RNA interference. J. Biol. 2, 27 (2003)

    Article  CAS  Google Scholar 

  10. Stanley, H., Botas, J. & Malhotra, V. The mechanism of Golgi segregation during mitosis is cell type-specific. Proc. Natl Acad. Sci. USA 94, 14467–14470 (1997)

    Article  CAS  ADS  Google Scholar 

  11. Shorter, J. & Warren, G. Golgi architecture and inheritance. Annu. Rev. Cell. Dev. Biol. 18, 379–420 (2002)

    Article  CAS  Google Scholar 

  12. Uhlmann, F. Separase regulation during mitosis. Biochem. Soc. Symp. 70, 243–251 (2003)

    Article  CAS  Google Scholar 

  13. Sharp, D. J. Cell division: MAST sails through mitosis. Curr. Biol. 12, R585–R587 (2002)

    Article  CAS  Google Scholar 

  14. Snaith, H. A., Armstrong, C. G., Guo, Y., Kaiser, K. & Cohen, P. T. Deficiency of protein phosphatase 2A uncouples the nuclear and centrosome cycles and prevents attachment of microtubules to the kinetochore in Drosophila microtubule star (mts) embryos. J. Cell Sci. 109, 3001–3012 (1996)

    CAS  PubMed  Google Scholar 

  15. Dilcher, M. et al. Use1p is a yeast SNARE protein required for retrograde traffic to the ER. EMBO J. 22, 3664–3674 (2003)

    Article  CAS  Google Scholar 

  16. Chua, J. J., Ng, M. M. & Chow, V. T. The non-structural 3 (NS3) protein of dengue virus type 2 interacts with human nuclear receptor binding protein and is associated with alterations in membrane structure. Virus Res. 102, 151–163 (2004)

    Article  CAS  Google Scholar 

  17. De Langhe, S., Haataja, L., Senadheera, D., Groffen, J. & Heisterkamp, N. Interaction of the small GTPase Rac3 with NRBP, a protein with a kinase-homology domain. Int. J. Mol. Med. 9, 451–459 (2002)

    CAS  PubMed  Google Scholar 

  18. Connolly, C. N., Futter, C. E., Gibson, A., Hopkins, C. R. & Cutler, D. F. Transport into and out of the Golgi complex studied by transfecting cells with cDNAs encoding horseradish peroxidase. J. Cell Biol. 127, 641–652 (1994)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank members of the Malhotra laboratory for discussions; members of the DRSC for advice; the Institute for Chemistry and Cell Biology for use of their Cybio robot; and J. Feramisco and members of the UCSD Cancer Center imaging facility for help with microscopy. Work in the Malhotra laboratory is supported by NIH grants and a senior investigator award from Sandler's Program for Asthma Research. N.P. is a Howard Hughes investigator.

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Correspondence to Vivek Malhotra.

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Reprints and permissions information is available at npg.nature.com/reprintsandpermissions. The authors declare no competing financial interests.

Supplementary information

Supplementary Figure 1

Golgi fragmentation and block in HRP secretion are not due to an arrest in mitosis. (PDF 541 kb)

Supplementary Table 1

1133 dsRNAs inducing a significant inhibition of HRP secretion. (PDF 97 kb)

Supplementary Table 2

154 dsRNAs tested in secondary screens and reasons for their removal. (PDF 36 kb)

Supplementary Table 3

130 genes involved in secretion and Golgi membrane organization. (PDF 32 kb)

Supplementary Legends

Text to accompany the above Supplementary Figure and Supplementary Tables. (DOC 40 kb)

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Bard, F., Casano, L., Mallabiabarrena, A. et al. Functional genomics reveals genes involved in protein secretion and Golgi organization. Nature 439, 604–607 (2006). https://doi.org/10.1038/nature04377

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