Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7162
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dc.contributor.authorKilo, Lukas-
dc.date.accessioned2022-07-07T12:21:56Z-
dc.date.available2022-07-07T12:21:56Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7176-
dc.description.abstractThe diversity of voltage gated calcium channel (VGCC) functions greatly outnumbers the count of voltage gated calcium channel genes. One of the ways to increase VGCC functional diversity is alternative splicing. In this thesis I could show for the Drosophila VGCC cacophony, a homolog to the vertebrate Cav2 calcium channel family, that functional diversity is indeed linked to alternative splicing. By using CRISPR/Cas for exon excision as well as electrophysiological methods, confocal microscopy, and behavioral assays, both isoform-specific properties and degenerate functions of exon dependent isoform subsets could be identified. Two alternative exon pairs encoding part of the voltage sensor or accessory subunit binding sites, respectively, were investigated. Differences in isoform localization as well as channel kinetics suggest a division of labor in some parts of the nervous system. Indeed, some of the isoforms fulfill essential functions with behavioral relevance, while others function in a degenerate manner. Although, whether these degenerate ones also exert unique functions under specific conditions remains to be determined. In addition to this, a novel collaborative interaction between two isoforms of the same gene could be discovered. Specifically, lethality resulting from the deletion of one essential isoform and behavioral impairments resulting from the deletion from the other alternative isoform are both fully rescued in trans heterozygous flies carrying both deletions. Both alternative exons have rather similar channel properties but different global and subcellular localizations. They are both required in concert throughout the nervous system for survival and normal motor behavior.en_GB
dc.language.isoengde
dc.rightsInCopyright*
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subject.ddc500 Naturwissenschaftende_DE
dc.subject.ddc500 Natural sciences and mathematicsen_GB
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.subject.ddc590 Tiere (Zoologie)de_DE
dc.subject.ddc590 Zoological sciencesen_GB
dc.titleRedundant, exclusive, and cooperative functions of alternative exons in Drosophila Cav2 channelsen_GB
dc.typeDissertationde
dc.identifier.urnurn:nbn:de:hebis:77-openscience-6d45d5b8-9ca1-4b89-bea7-5df7855f9a3e1-
dc.identifier.doihttp://doi.org/10.25358/openscience-7162-
jgu.type.dinitypedoctoralThesisen_GB
jgu.type.versionOriginal workde
jgu.type.resourceTextde
jgu.date.accepted2022-03-
jgu.description.extentVII, 130 Seiten, Illustrationende
jgu.organisation.departmentFB 10 Biologiede
jgu.organisation.year2021-
jgu.organisation.number7970-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.organisation.placeMainz-
jgu.subject.ddccode500de
jgu.subject.ddccode570de
jgu.subject.ddccode590de
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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