Skip Navigation


Human Molecular Genetics Advance Access originally published online on March 28, 2006
Human Molecular Genetics 2006 15(9):1513-1523; doi:10.1093/hmg/ddl072
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
15/9/1513    most recent
ddl072v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (6)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Van Raamsdonk, J. M.
Right arrow Articles by Hayden, M. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Van Raamsdonk, J. M.
Right arrow Articles by Hayden, M. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Body weight is modulated by levels of full-length Huntingtin

Jeremy M. Van Raamsdonk1,2, William T. Gibson1,2, Jacqueline Pearson1,2, Zoe Murphy1,2, Ge Lu1,2, Blair R. Leavitt1,2 and Michael R. Hayden1,2,*

1Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada V6T 1Z3 and 2Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, 980 West 28th Avenue, Vancouver, BC, Canada V5Z 4H4

* To whom correspondence should be addressed. Tel: +604 8753535; Fax: +604 8753819; Email: mrh{at}cmmt.ubc.ca

Received January 24, 2006; Accepted March 19, 2006

Huntington disease is an adult-onset neurodegenerative disorder that is caused by the expansion of a polyglutamine tract within the Huntingtin (htt) protein. Wild-type htt has been shown to be involved in transcription, transport and cell survival. Here, we demonstrate that increased expression of full-length wild-type htt in mice is associated with a dose-dependent increase in body weight which results from an increase in both total fat mass and fat-free mass. Conversely, we show that a reduction in the levels of wild-type htt is associated with decreased body weight. Examination of individual organ weights revealed that the weight of the heart, liver, kidneys, lungs and spleen increased with the over-expression of wild-type htt, whereas the brain and testis were unaltered. On the basis of these initial findings, we examined mice that over-express full-length mutant htt to determine the effect of polyglutamine expansion on this novel function of wild-type htt. We found that over-expression of full-length mutant htt, but not an N-terminal fragment of mutant htt, also increased body weight and organ weight, except in the brain and testis where mutant htt appears to be toxic. In these mice, the majority of weight gain could be accounted for by increases in total fat mass. Further investigation of the weight gain phenotype revealed that the increases in weight were not accounted for by increased food consumption relative to body weight. Overall, we demonstrate that increased levels of both wild-type and mutant full-length htt are associated with increased body weight.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Neurosci.Home page
Y. Dai, N. L. Dudek, Q. Li, S. C. Fowler, and N. A. Muma
Striatal Expression of a Calmodulin Fragment Improved Motor Function, Weight Loss, and Neuropathology in the R6/2 Mouse Model of Huntington's Disease
J. Neurosci., September 16, 2009; 29(37): 11550 - 11559.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
N. A. Aziz, J.M.M. van der Burg, G. B. Landwehrmeyer, P. Brundin, T. Stijnen, EHDI Study Group, and R. A.C. Roos
Weight loss in Huntington disease increases with higher CAG repeat number
Neurology, November 4, 2008; 71(19): 1506 - 1513.
[Abstract] [Full Text] [PDF]


Home page
Proc R Soc BHome page
K. Littin, A. Acevedo, W. Browne, J. Edgar, M. Mendl, D. Owen, C. Sherwin, H. Wurbel, and C. Nicol
Towards humane end points: behavioural changes precede clinical signs of disease in a Huntington's disease model
Proc R Soc B, August 22, 2008; 275(1645): 1865 - 1874.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Gray, D. I. Shirasaki, C. Cepeda, V. M. Andre, B. Wilburn, X.-H. Lu, J. Tao, I. Yamazaki, S.-H. Li, Y. E. Sun, et al.
Full-Length Human Mutant Huntingtin with a Stable Polyglutamine Repeat Can Elicit Progressive and Selective Neuropathogenesis in BACHD Mice
J. Neurosci., June 11, 2008; 28(24): 6182 - 6195.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.