Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/28337
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dc.titleAsymmetric cell division in the drosophila embryonic neuroblast
dc.contributor.authorLEE SIEW CHING JOAN
dc.date.accessioned2011-11-08T18:04:30Z
dc.date.available2011-11-08T18:04:30Z
dc.date.issued2009-06-06
dc.identifier.citationLEE SIEW CHING JOAN (2009-06-06). Asymmetric cell division in the drosophila embryonic neuroblast. ScholarBank@NUS Repository.
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/28337
dc.description.abstractA novel coiled-coil protein, Spindle Miranda (Spim) or Drosophila CG9646 protein, was isolated from a microarray screen for potential effectors of telophase rescue in the insc mutant background. Both Spim and Insc are positively regulated by the Snail family of transcription factors. Single mutants of spim do not exhibit any defects in development or asymmetric division. Only spim insc double mutant embryos manifest abnormalities like delayed development and severe mislocalization of Mira/Pros to the mitotic spindle in mitotic metaphase NBs. These findings strongly support the existence of a genetic interaction between Spim and Insc in the NB, as Insc is specifically expressed in NBs. The genetic interaction between Spim and Insc is involved in targeting Mira/Pros to the basal cortex in mitotic NBs, possibly by stabilizing the actin cytoskeleton and interacting with Lgl and Non-muscle myosin II. The Spim-Insc genetic interaction is required for Pins expression and may also have role in cell cycle regulation and development.
dc.language.isoen
dc.subjectAsymmetric division, Drosophila neuroblast
dc.typeThesis
dc.contributor.departmentNUS GRAD SCH FOR INTEGRATIVE SCI & ENGG
dc.description.degreePh.D
dc.description.degreeconferredDOCTOR OF PHILOSOPHY
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Ph.D Theses (Open)

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