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Ric-8 controls Drosophila neural progenitor asymmetric division by regulating heterotrimeric G proteins

Nature Cell Biology volume 7, pages 1091–1098 (2005)Cite this article

Abstract

Asymmetric division of Drosophila neuroblasts (NBs) and the Caenorhabditis elegans zygote uses polarity cues provided by the Par proteins, as well as heterotrimeric G-protein-signalling that is activated by a receptor-independent mechanism mediated by GoLoco/GPR motif proteins1,2. Another key component of this non-canonical G-protein activation mechanism is a non-receptor guanine nucleotide-exchange factor (GEF) for Gα, RIC-8, which has recently been characterized in C. elegans and in mammals3,4,5,6. We show here that the Drosophila Ric-8 homologue is required for asymmetric division of both NBs and pI cells. Ric-8 is necessary for membrane targeting of Gαi, Pins and Gβ13F, presumably by regulating multiple Gα subunit(s). Ric-8 forms an in vivo complex with Gαi and interacts preferentially with GDP–Gαi, which is consistent with Ric-8 acting as a GEF for Gαi. Comparisons of the phenotypes of Gαi, Ric-8, Gβ13F single and Ric-8;Gβ13F double loss-of-function mutants indicate that, in NBs, Ric-8 positively regulates Gαi activity. In addition, Gβγ acts to restrict Gαi (and GoLoco proteins) to the apical cortex, where Gαi (and Pins) can mediate asymmetric spindle geometry.

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Figure 1: Ric-8 interacts preferentially with GDP–Gαi and complexes with Gαi and Pins.
Figure 2: Ric-8 is required for the asymmetric division of NBs by regulating membrane localization of Gαi and Pins.
Figure 3: Ric-8 is required for the asymmetric division of pI cells and Ric-8 is distributed in the cytosol in both NBs and pI cells.
Figure 4: Ric-8 is required for cortical localization and stability of Gβ13F.
Figure 5: ric-8;Gβ13F double GLC NBs display defects similar to NBs lacking ric-8 or Gαi function.

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Acknowledgements

We thank H. Bellen, C.Q. Doe, D. Glover, Y.N. Jan, D. St Johnston, T. Kaufman, C. Klambt, J.A. Knoblich, E. Knust, F. Matsuzaki, S. Roth, F. Schweisguth, X. Yang, A. Wodarz, Developmental Studies Hybridoma Bank (University of Iowa) and the Bloomington Stock Center for generously providing antibodies and fly stocks. We thank F. S. Willard for discussion and support, and W. Chia thanks Y. Cai for stimulating discussions. This work was supported by Temasek Life Sciences Laboratory, Singapore Millennium Foundation (F. Y.) and Wellcome Trust (W. C.).

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Authors and Affiliations

  1. Temasek Life Sciences Laboratory, 1 Research Link, National University of Singapore, Singapore, 117604

    Hongyan Wang, Kian Hong Ng, Hongliang Qian, William Chia & Fengwei Yu

  2. Department of Pharmacology, Lineberger Comprehensive Cancer Center and UNC Neuroscience Center, The University of North Carolina at Chapel Hill, Chapel Hill, 27599, NC, USA

    David P. Siderovski

  3. Department of Biological Sciences, National University of Singapore, Singapore, 117604

    William Chia & Fengwei Yu

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Correspondence to William Chia or Fengwei Yu.

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Wang, H., Ng, K., Qian, H. et al. Ric-8 controls Drosophila neural progenitor asymmetric division by regulating heterotrimeric G proteins. Nat Cell Biol 7, 1091–1098 (2005). https://doi.org/10.1038/ncb1317

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