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Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster

Synaptic transmission of the single gene mutant, shibirets1 (shi), of Drosophila melanogaster is reversibly blocked by elevated temperature. The presynaptic mechanism of transmission was studied in the neuromuscular junction of the dorsal longitudinal flight muscle of this mutant. It was observed th...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1983
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112451/
https://www.ncbi.nlm.nih.gov/pubmed/6304107
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collection PubMed
description Synaptic transmission of the single gene mutant, shibirets1 (shi), of Drosophila melanogaster is reversibly blocked by elevated temperature. The presynaptic mechanism of transmission was studied in the neuromuscular junction of the dorsal longitudinal flight muscle of this mutant. It was observed that when the temperature was raised to 29 degrees C in shi flies, the amplitude of the excitatory junction potential (EJP) greatly diminished, the frequency of spontaneously released miniature excitatory junction potentials (MEJP's) was greatly reduced, and almost complete vesicle depletion was observed. These conditions were reversible if the temperature was lowered to 19 degrees C. These data suggest that the block in transmission is a result of vesicle depletion. It is suggested that depletion occurs not as a result of excessive release of transmitter but rather as a result of a block in the recycling of vesicles, which causes depletion as exocytosis (transmitter release) proceeds normally.
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spelling pubmed-21124512008-05-01 Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster J Cell Biol Articles Synaptic transmission of the single gene mutant, shibirets1 (shi), of Drosophila melanogaster is reversibly blocked by elevated temperature. The presynaptic mechanism of transmission was studied in the neuromuscular junction of the dorsal longitudinal flight muscle of this mutant. It was observed that when the temperature was raised to 29 degrees C in shi flies, the amplitude of the excitatory junction potential (EJP) greatly diminished, the frequency of spontaneously released miniature excitatory junction potentials (MEJP's) was greatly reduced, and almost complete vesicle depletion was observed. These conditions were reversible if the temperature was lowered to 19 degrees C. These data suggest that the block in transmission is a result of vesicle depletion. It is suggested that depletion occurs not as a result of excessive release of transmitter but rather as a result of a block in the recycling of vesicles, which causes depletion as exocytosis (transmitter release) proceeds normally. The Rockefeller University Press 1983-06-01 /pmc/articles/PMC2112451/ /pubmed/6304107 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster
title Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster
title_full Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster
title_fullStr Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster
title_full_unstemmed Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster
title_short Reversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster
title_sort reversible control of synaptic transmission in a single gene mutant of drosophila melanogaster
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112451/
https://www.ncbi.nlm.nih.gov/pubmed/6304107