Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/17759
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dc.coverage.spatialBiologyen_US
dc.date.accessioned2014-04-16T04:57:43Z-
dc.date.available2014-04-16T04:57:43Z-
dc.date.issued2014-04-16-
dc.identifier.urihttp://hdl.handle.net/10603/17759-
dc.description.abstractThe nuclear envelope forms a distinct boundary between the nucleus and newlinecytoplasm in all eukaryotic cells. It has a complex organization consisting of the inner and newlineouter nuclear membranes, nuclear pore complexes and the nuclear lamina. The nuclear lamina newlineis a fibrous network of proteins that lines the inner nuclear membrane and performs essential newlinefunctions during envelope disassembly and assembly at mitosis. The lamina also provides newlineattachment sites for the interphase chromatin. The pore complexes provide channels for newlinemolecular exchange between the nucleus and cytoplasm. newlineNuclear import of proteins is a selective and energy-dependent process, requiring newlinethe presence of a nuclear localization signal (NLS) on the karyophilic protein. Transport newlineoccurs in at least two steps. The first step, binding to the pore, is due to specific recognition newlineof the transport signal and does not require A TP. The second step, translocation through the newlinepore, is ATP-dependent. newlineThe major structural proteins of the nuclear lamina are the nuclear lamins. The newlinevertebrate lamins can be grouped into A-type and B-type lamins. While B-type lamins are newlineconstitutively expressed, the expression of A-type lamins is regulated during development. newlineThe purpose of undertaking this work was firstly, to identify membrane-anchorage newlinesites of the nuclear lamina using chemical cross-linking agents. Secondly, the nuclear newlineenvelope-associated ATPase was studied in relation to the effect of NLS-receptor interaction newlineon its activity. Thirdly, the expression oflamins during rat liver development was determined newlineusing an antibody raised against bacterially-expressed laminA protein. Finally, the expression newlineof a specific class of pore complex proteins during development was studied, and the ability newlineVll newlineof antibodies to these proteins to block transport of nuclear proteins was tested in an in vitro newlineassay. newlineThe thesis is divided into four chapters and the contents of each chapter, in brief, newlineare given below.en_US
dc.format.extent123p.en_US
dc.languageEnglishen_US
dc.relation-en_US
dc.rightsuniversityen_US
dc.titleThe nuclear lamina and pore complex organizationen_US
dc.title.alternative-en_US
dc.creator.researcherFatima, Soghraen_US
dc.subject.keywordMolecular Biologyen_US
dc.subject.keywordnuclear laminaen_US
dc.subject.keywordorganizationen_US
dc.subject.keywordpore complexen_US
dc.description.noteBibliography p.109-123en_US
dc.contributor.guidePatnaik, Veenaen_US
dc.publisher.placeDelhien_US
dc.publisher.universityJawaharlal Nehru Universityen_US
dc.publisher.institutionCentre for Cellular and Molecular Biologyen_US
dc.date.registeredn.d.en_US
dc.date.completed1995en_US
dc.date.awardedn.d.en_US
dc.format.dimensions-en_US
dc.format.accompanyingmaterialNoneen_US
dc.type.degreePh.D.en_US
dc.source.inflibnetINFLIBNETen_US
Appears in Departments:Centre for Cellular and Molecular Biology

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01_title.pdfAttached File20.58 kBAdobe PDFView/Open
02_certificate.pdf24 kBAdobe PDFView/Open
03_dedication.pdf15.07 kBAdobe PDFView/Open
04_acknowledgemets.pdf42.73 kBAdobe PDFView/Open
05_contents.pdf108.97 kBAdobe PDFView/Open
06_abstract.pdf134.17 kBAdobe PDFView/Open
07_list of publications.pdf21.06 kBAdobe PDFView/Open
08_list of figures.pdf48.81 kBAdobe PDFView/Open
09_list of tables.pdf17.15 kBAdobe PDFView/Open
10_list of abbreviations.pdf44.58 kBAdobe PDFView/Open
11_chapter 1.pdf1.46 MBAdobe PDFView/Open
12_chapter 2.pdf686.78 kBAdobe PDFView/Open
13_chapter 3.pdf10.4 MBAdobe PDFView/Open
14_references.pdf668.66 kBAdobe PDFView/Open


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