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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/1990
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dc.contributor.authorTare, Meghana-
dc.date.accessioned2021-09-09T03:26:03Z-
dc.date.available2021-09-09T03:26:03Z-
dc.date.issued2012-10-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/dvg.22355-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/1990-
dc.description.abstractGenetic mosaic approach is commonly used in the Drosophila eye by completely abolishing or misexpressing a gene within a subset of cells to unravel its role during development. Classical genetic mosaic approach involves random clone generation in all developing fields. Consequently, a large sample size needs to be screened to generate and analyze clones in specific domains of the developing eye. To address domain specific functions of genes during axial patterning, we have developed a system for generating mosaic clones by combining Gal4/UAS and flippase (FLP)/FRT system which will allow generation of loss-of-function as well as gain-of-function clones on the dorsal and ventral eye margins. We used the bifid-Gal4 driver to drive expression of UAS-FLP. This reagent can have multiple applications in (i) studying spatio-temporal function of a gene during dorso-ventral (DV) axis specification in the eye, (ii) analyzing genetic epistasis of genes involved in DV patterning, and (iii) conducting genome wide screens in a domain specific manner. genesis 51:68–74, 2013. © 2012 Wiley Periodicals, Inc.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectBiologyen_US
dc.subjectDorso-Ventral axisen_US
dc.subjectDrosophila Eyeen_US
dc.subjectpatterningen_US
dc.subjectGenetic mosaicen_US
dc.subjectGal4/UAS techniqueen_US
dc.titleDomain specific genetic mosaic system in the Drosophila eyeen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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