Dr Jennifer Waby
Lecturer in Biomedical Science
Biomedical Sciences Group
Room number: 115
Department of Biological Sciences
The University of Hull
HU6 7RX UK
Tel:+44 (0)1482 46 2062
Fax: +44 (0)1482 46 5458
Email: j.waby@hull.ac.uk
Research Interests
My research interests focus on a family of
transcription factors known as the Sp family. The founder member of
this family, Sp1, is a ubiquitously expressed transcription factor
whose expression is reported to be upregulated in a number of
cancers. Sp1 regulates expression of genes involved in cell cycle
regulation, apoptosis, and lipid neogenesis, all important pathways
in cancer development and embryogenesis. The importance of Sp1 in
embryogenesis is highlighted by the observation that Sp1 knockdown
is embryonic lethal in mice. I am specifically interested in how
Sp1-mediated gene regulation is controlled in development and how
this correlates with Sp1 regulation in tumour progression. My
previous work has revealed that Sp1 acetylation attenuates Sp1
binding at the Bak and P21 promoters, which alters transcriptional
activation. The Sp1 acetylation site is highly conserved within the
Sp family and my current research aims to investigate the effects
of acetylation on the binding activities of other Sp-family members
and their potential roles in cancer.
Brief CV
- Postdoctoral Research
Associate (2006-2010), Human Nutrition Unit, University of
Sheffield. Employed by Dr. Bernard Corfe, working on BBSRC and FSA
funded projects.
- Ph.D. Neuroscience
(2002-2006), University of Sheffield.
- B.Sc. (Hons) Neuroscience (1999-2002), University of
Sheffield
Selected Publications
Waby JS,
Chirakkal H, Yu CW, Griffiths GJ, Benson RSP, Bingle CD, Corfe BM.
Sp1 acetylation results in loss of DNA binding at promoters
associated with cell cycle arrest and cell death in a colon cell
line. Molecular Cancer: In press.
Yu CW, Waby JS, Chirakkal H,
Staton CA and Corfe BM (2010). Butyrate suppresses expression of
neuropilin I in colorectal cell lines through inhibition of Sp1
transactivation. Molecular Cancer: In press.
Waby JS,
Bingle BD & Corfe BM (2008) Post-Translational Control of
Sp-Family Transcription Factors. Current Genomics 5:
301-311.
Chirakkal H, Leech SH,
Brookes KE, Prais AL, Waby JS, Corfe BM. (2006)
Upregulation of BAK by butyrate in the colon is associated with
increased Sp3 binding. Oncogene 25: 7192-200.
Ackerley S, Grierson AJ, Banner
S, Perkinton MS, Brownlees J, Byers HL, Ward M, Thornhill P,
Hussain K, Waby JS, Anderton BH, Cooper JD,
Dingwall C, Leigh PN, Shaw CE, Miller CC (2004). p38alpha
stress-activated protein kinase phosphorylates neurofilaments and
is associated with neurofilament pathology in amyotrophic lateral
sclerosis. Mol Cell Neurosci 26 (2): 354-64.
Teaching
|
Module number
|
Module name
|
Role
|
Level
|
| 58962 |
Advanced Reviews in Biomedical Science |
Module coordinator |
7 |
| 58278 |
Contemporary issues in Biology |
Facilitator |
5 |
| 58327 |
20 credit research project |
Supervisor |
6
|
| 58174 |
Skills for Biologists |
Tutor |
4 |
| 58271 |
Immunology & Proteomics |
Lecturer |
5 |
Administrative duties
Timetable officer
Page last updated by Jennifer Waby on
10/1/2010