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The identification of genetic loci that interact with the neural selector gene <italic>cut</italic> during wing margin development in <italic>Drosophila melanogaster</italic>.

dc.contributor.authorKrupp, Joshua J.
dc.contributor.advisorRaymond, Pamela A.
dc.contributor.advisorBodmer, Rolf A.
dc.date.accessioned2016-08-30T15:50:41Z
dc.date.available2016-08-30T15:50:41Z
dc.date.issued2005
dc.identifier.urihttp://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:3186674
dc.identifier.urihttps://hdl.handle.net/2027.42/125128
dc.description.abstractThe <italic>Drosophila melanogaster</italic> selector gene <italic>cut </italic> is a hierarchal regulator of external sensory organ identity, and is required to pattern sensory and non-sensory cells of the wing margin. <italic> cut</italic> performs the latter function, in part, by maintaining expression of the secreted morphogen encoded by <italic>wingless</italic>. I find that cut is required for wing margin sensory organ specification in addition to and independent of <italic>wingless</italic> maintenance. In addition, I performed a genetic modifier screen to identify other genes that interact with <italic> cut</italic> in the regulation of wing margin patterning. In total, 45 genetic loci (35 gain-of-function and 10 loss-of-function) were identified by virtue of their ability to suppress the wing margin defects resulting from <italic> gypsy</italic> retrotransposon-mediated insulation of the <italic>cut</italic> wing margin enhancer. Further genetic characterization identified several subgroups of candidate <italic>cut</italic> interacting loci. One group consists of putative regulators of <italic>gypsy</italic> insulator activity. A second group is potentially required for the regulation of cut expression and/or activity, which includes <italic>longitudinals lacking</italic>, a gene encoding for a BTB-domain zinc-finger transcription factor. A third group, which includes a component of the Brahma chromatin remodeling complex encoded by <italic> moira</italic>, affects the level of <italic>cut</italic> expression/activity in two opposing ways, by suppressing <italic>gypsy</italic>-mediated <italic> ct<super>K</super></italic> phenotype and enhancing the non-<italic>gypsy ct<super>53d</super></italic> phenotype. This suggests enhancer controlled transcription and gypsy mediated insulation, at least of the cut locus, may utilize common components to regulate gene expression.
dc.format.extent151 p.
dc.languageEnglish
dc.language.isoEN
dc.subjectCut
dc.subjectDevelopment
dc.subjectDrosophila
dc.subjectExternal Sensory Organs
dc.subjectGenetic
dc.subjectIdentification
dc.subjectInteract
dc.subjectLoci
dc.subjectMelanogaster
dc.subjectNeural Selector Gene
dc.subjectSelector Genes
dc.subjectWing Margin
dc.titleThe identification of genetic loci that interact with the neural selector gene <italic>cut</italic> during wing margin development in <italic>Drosophila melanogaster</italic>.
dc.typeThesis
dc.description.thesisdegreenamePhDen_US
dc.description.thesisdegreedisciplineBiological Sciences
dc.description.thesisdegreedisciplineGenetics
dc.description.thesisdegreedisciplineNeurosciences
dc.description.thesisdegreegrantorUniversity of Michigan, Horace H. Rackham School of Graduate Studies
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/125128/2/3186674.pdf
dc.owningcollnameDissertations and Theses (Ph.D. and Master's)


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