Skip navigation
  • Home
  • Browse
    • Communities
      & Collections
    • Browse Items by:
    • Publication Date
    • Author
    • Title
    • Subject
    • Department
  • Sign on to:
    • My MacSphere
    • Receive email
      updates
    • Edit Profile


McMaster University Home Page
  1. MacSphere
  2. Open Access Dissertations and Theses Community
  3. Open Access Dissertations and Theses
Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/8339
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorMak, S.en_US
dc.contributor.authorSchaller, Daniel Michaelen_US
dc.date.accessioned2014-06-18T16:42:37Z-
dc.date.available2014-06-18T16:42:37Z-
dc.date.created2010-11-25en_US
dc.date.issued1990-09en_US
dc.identifier.otheropendissertations/3551en_US
dc.identifier.other4568en_US
dc.identifier.other1662438en_US
dc.identifier.urihttp://hdl.handle.net/11375/8339-
dc.description.abstract<p>It is well documented that two regions of the human adenoviruses, each encoding multiple polypeptides, are responsible for the transforming activity of these viruses and that these genes are essential for the efficient production of virus in permissively infected cells. This study was undertaken to examine the importance of the individual proteins of one of these regions from adenovirus serotype 12 (Ad12), the E1b region, in lytic infection and transformation. Molecular defects have been identified in the smaller protein, the 19K, in two of the cytocidal (cyt) mutants of Ad12. Direct evidence has been obtained demonstrating that the point mutation in the 19K of one of the mutants is sufficient to cause the degradation of DNA in infected KB cells and reduce the transforming activity of the mutant virus and perhaps its tumourigenic potential, which are characteristic phenotypes of the cyt mutants. A mutation was also engineered in the larger, 55K E1b protein and was found to impair viral DNA replication, reduce the expression of the late, structural proteins of the virus and block the inhibition of cellular protein synthesis which is normally observed upon infection of KB cells with the wild type virus. The 55K was also found to be necessary for the efficient expression of the early genes of the virus, particularly the E2b gene, which encodes essential proteins for viral DNA replication. The multiplicity dependent leakiness of the DNA replication defect of this mutant was exploited to separate the DNA replication defect from the defects in late protein expression and shut off of host protein synthesis. The observation that this mutant exhibited 1% of the transforming activity of the wild type virus but that transformants were fully tumourigenic also separated a transformation function from a tumourigenic function of this protein.</p>en_US
dc.subjectBiologyen_US
dc.subjectBiologyen_US
dc.titleThe Role of the E1b Gene Products of Adenovirus Serotype 12 in Lytic Infection and Transformationen_US
dc.typethesisen_US
dc.contributor.departmentBiologyen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
Appears in Collections:Open Access Dissertations and Theses

Files in This Item:
File SizeFormat 
fulltext.pdf
Open Access
9.34 MBAdobe PDFView/Open
Show simple item record Statistics


Items in MacSphere are protected by copyright, with all rights reserved, unless otherwise indicated.

Sherman Centre for Digital Scholarship     McMaster University Libraries
©2022 McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L8 | 905-525-9140 | Contact Us | Terms of Use & Privacy Policy | Feedback

Report Accessibility Issue