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© The Rockefeller University Press,
0021-9525/2000//905 $5.00
The Journal of Cell Biology, Volume 151, Number 4,
, 2000 905-918
Original Article |
Lava Lamp, a Novel Peripheral Golgi Protein, Is Required for Drosophila melanogaster Cellularization
Drosophila cellularization and animal cell cytokinesis rely on the coordinated functions of the microfilament and microtubule cytoskeletal systems. To identify new proteins involved in cellularization and cytokinesis, we have conducted a biochemical screen for microfilament/microtubule-associated proteins (MMAPs). 17 MMAPs were identified; seven have been previously implicated in cellularization and/or cytokinesis, including KLP3A, Anillin, Septins, and Dynamin. We now show that a novel MMAP, Lava Lamp (Lva), is also required for cellularization. Lva is a coiled-coil protein and, unlike other proteins previously implicated in cellularization or cytokinesis, it is Golgi associated. Our functional analysis shows that cellularization is dramatically inhibited upon injecting anti–Lva antibodies (IgG and Fab) into embryos. In addition, we show that brefeldin A, a potent inhibitor of membrane trafficking, also inhibits cellularization. Biochemical analysis demonstrates that Lva physically interacts with the MMAPs Spectrin and CLIP190. We suggest that Lva and Spectrin may form a Golgi-based scaffold that mediates the interaction of Golgi bodies with microtubules and facilitates Golgi-derived membrane secretion required for the formation of furrows during cellularization. Our results are consistent with the idea that animal cell cytokinesis depends on both actomyosin-based contraction and Golgi-derived membrane secretion.
Key Words: cytokinesis cytoskeleton Spectrin KLP3A and brefeldin A
© 2000 The Rockefeller University Press
Abbreviations used in this paper: ABP, actin-binding protein; BFA, brefeldin A; GST, glutathione-S-transferase; Lva, Lava Lamp; MHC, myosin heavy chain; MMAP, microfilament/microtubule-associated protein; MP, microprojection; MS/MS, tandem mass spectrometry analysis; MT, microtubule; Myo-GFP, myosin II–green fluorescent protein; PM, plasma membrane.
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