Scramblases are a family of single-pass plasma membrane proteins, identified by their purported ability to scramble phospholipids across the two layers of plasma membrane isolated from platelets and red blood cells. However, their true in vivo role has yet to be elucidated. We report the generation and isolation of null mutants of two Scramblases identified in Drosophila melanogaster. We demonstrate that flies lacking either or both of these Scramblases are not compromised in vivo in processes requiring scrambling of phospholipids. Instead, we show that D. melanogaster lacking both Scramblases have more vesicles and display enhanced recruitment from a reserve pool of vesicles and increased neurotransmitter secretion at the larval neuromuscular synapses. These defects are corrected by the introduction of a genomic copy of the Scramb 1 gene. The lack of phenotypes related to failure of scrambling and the neurophysiological analysis lead us to propose that Scramblases play a modulatory role in the process of neurotransmission.
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10 April 2006
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April 10 2006
Drosophila melanogaster Scramblases modulate synaptic transmission
Usha Acharya,
Usha Acharya
1Laboratory of Protein Dynamics and Signaling, National Cancer Institute Frederick, Frederick, MD 21702
2Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, MA 01605
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Michael Beth Edwards,
Michael Beth Edwards
1Laboratory of Protein Dynamics and Signaling, National Cancer Institute Frederick, Frederick, MD 21702
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Ramon A. Jorquera,
Ramon A. Jorquera
3Centro de Estudios Científicos, Valdivia 511-0246, Chile
5Universidad Austral de Chile, Valdivia 509-9200, Chile
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Hugo Silva,
Hugo Silva
3Centro de Estudios Científicos, Valdivia 511-0246, Chile
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Kunio Nagashima,
Kunio Nagashima
4EM Facility/Image Analysis Laboratory, Science Applications International Corporation Frederick, Frederick, MD 21702
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Pedro Labarca,
Pedro Labarca
3Centro de Estudios Científicos, Valdivia 511-0246, Chile
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Jairaj K. Acharya
Jairaj K. Acharya
1Laboratory of Protein Dynamics and Signaling, National Cancer Institute Frederick, Frederick, MD 21702
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Usha Acharya
1Laboratory of Protein Dynamics and Signaling, National Cancer Institute Frederick, Frederick, MD 21702
2Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, MA 01605
Michael Beth Edwards
1Laboratory of Protein Dynamics and Signaling, National Cancer Institute Frederick, Frederick, MD 21702
Ramon A. Jorquera
3Centro de Estudios Científicos, Valdivia 511-0246, Chile
5Universidad Austral de Chile, Valdivia 509-9200, Chile
Hugo Silva
3Centro de Estudios Científicos, Valdivia 511-0246, Chile
Kunio Nagashima
4EM Facility/Image Analysis Laboratory, Science Applications International Corporation Frederick, Frederick, MD 21702
Pedro Labarca
3Centro de Estudios Científicos, Valdivia 511-0246, Chile
Jairaj K. Acharya
1Laboratory of Protein Dynamics and Signaling, National Cancer Institute Frederick, Frederick, MD 21702
Correspondence to Jairaj K. Acharya: [email protected]
M.B. Edwards, R. Jorquera, and H. Silva contributed equally to this paper.
Abbreviations used in this paper: dsRNA, double-stranded RNA; ECP, exo/endo pool of SVs; EMS, ethyl methane sulfonate; GMR, glass multimer reporter; NMJ, neuromuscular junction; PS, phosphatidylserine; PTP, posttetanic potentiation; RP, reserve pool; S2 cells, Schneider cells; SV, synaptic vesicle; UAS, upstream activating sequence.
Received:
June 24 2005
Accepted:
March 08 2006
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2006
J Cell Biol (2006) 173 (1): 69–82.
Article history
Received:
June 24 2005
Accepted:
March 08 2006
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Citation
Usha Acharya, Michael Beth Edwards, Ramon A. Jorquera, Hugo Silva, Kunio Nagashima, Pedro Labarca, Jairaj K. Acharya; Drosophila melanogaster Scramblases modulate synaptic transmission . J Cell Biol 10 April 2006; 173 (1): 69–82. doi: https://doi.org/10.1083/jcb.200506159
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