Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/67927
Title: Linking aberrant splicing to cardiac aging : unravelling SRPK2
Authors: Meroshini, M.
Keywords: DRNTU::Science
Issue Date: 2016
Abstract: The gradual and inevitable process of aging can lead to detrimental effects such as disruptions in cellular processes and accumulation of damage in cells. It has been shown that the number of alternatively spliced genes significantly increases with age, and that aberrant splicing is one of the major causes of a few age-related diseases such as Hutchinson-Gilford progeria syndrome (HGPS), frontotemporal lobar degeneration (FTLD), or Alzheimer's disease (AD). Identification of the key players in splicing can lead to a better understanding of the relationship between aberrant splicing and cardiac aging. One essential component of the splicing process is SRPK2, a member of the the Serine-Arginine Rich Protein Kinase (SRPK) family. A thorough understanding of SRPK2, its interactors, its regulatory mechanism, and its functions the aim of this project. With methods such as BioID proximity labelling, western blots, immunoprecipitation and real time PCR, a few possible interactors of SRPK2 have been short listed, and the regulatory mechanism of SRPK2 cellular levels have been proposed.
URI: http://hdl.handle.net/10356/67927
Rights: Nanyang Technological University
Fulltext Permission: restricted
Fulltext Availability: With Fulltext
Appears in Collections:SBS Student Reports (FYP/IA/PA/PI)

Files in This Item:
File Description SizeFormat 
Linking Aberrant Splicing to Cardiac Aging – Unravelling SRPK2.pdf
  Restricted Access
5.23 MBAdobe PDFView/Open

Google ScholarTM

Check

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.