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/11375/9172
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorZhu, Xu-Dongen_US
dc.contributor.authorAsa, Taliaen_US
dc.date.accessioned2014-06-18T16:45:56Z-
dc.date.available2014-06-18T16:45:56Z-
dc.date.created2011-05-31en_US
dc.date.issued2010-07en_US
dc.identifier.otheropendissertations/4319en_US
dc.identifier.other5337en_US
dc.identifier.other2039702en_US
dc.identifier.urihttp://hdl.handle.net/11375/9172-
dc.description.abstract<p>Recent data suggest that protein arginine methyltransferase 1 (PRMT1) plays a role in telomere length maintenance and telomere stability. PRMT1 has been shown to methylate the basic domain of TRF2 and depletion of PRMT1 leads to the formation of telomere doublets in primary cells and telomere shortening in cancer cells. Additionally mass spectrometry data suggest candidate arginine residues in TRF1 and TRF2 that are mono- or di-methylated. These data suggest that arginine methylation and thus PRMT enzymes may playa role in telomere biology.</p> <p>Because PRMT1 has been shown to play a role in telomere maintenance, we decided to look for a role of another PRMT enzyme, coactivator associated arginine methyltransferase 1 (CARM1), on telomere biology. To determine if CARM1 plays a role in telomere length maintenance, hTERT-BJ cells were depleted for CARM1. Initially, a senescent phenotype was observed; however, this phenotype was not reproducible. Subsequently, I have shown that these cells do not accumulate telomere or genomic instability or a change in growth. To determine if CARM1 plays a role in telomere length maintenance, hTERT-BJ, HeLaII, and MCF-7 cells were depleted of CARM1 and cultured long term. Southern blot analysis indicated no change in telomere length dynamics over time upon depletion of CARM1 compared to control cells. Thus these results suggest that CARM1 does not playa role in telomere length maintenance.</p> <p>The laboratory of Linger identified telomeres to be transcribed into telomere repeat-containing RNA termed TERRA. The mechanism of TERRA regulation is still to be elucidated. Because CARM1 is a transcriptional coactivator, we hypothesized that CARM1 play a role in TERRA transcription. Northern blot analysis conducted in hTERT-BJ and MCF-7 cells depleted of CARM1 revealed no role for CARM1 in TERRA regulation.</p>en_US
dc.subjectBiologyen_US
dc.subjectBiologyen_US
dc.titleAnalysis of the role of CARM1 in telomere maintenanceen_US
dc.typethesisen_US
dc.contributor.departmentBiologyen_US
dc.description.degreeMaster of Science (MS)en_US
Appears in Collections:Open Access Dissertations and Theses

Files in This Item:
File SizeFormat 
fulltext.pdf
Open Access
36.82 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