This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Phesse, T. J.
Right arrow Articles by Clarke, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Phesse, T. J.
Right arrow Articles by Clarke, A. R.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, October 2008, p. 6094-6103, Vol. 28, No. 19
0270-7306/08/$08.00+0     doi:10.1128/MCB.00539-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Deficiency of Mbd2 Attenuates Wnt Signaling{triangledown} ,{dagger}

Toby J. Phesse,1,{ddagger} Lee Parry,1 Karen R. Reed,1 Kenneth B. Ewan,1 Trevor C. Dale,1 Owen J. Sansom,2 and Alan R. Clarke1*

Cardiff School of Biosciences, Cardiff University, Cardiff CF10 3US, United Kingdom,1 The Beatson Institute, Garscube Estate, Glasgow G61 1BD, United Kingdom2

Received 2 April 2008/ Returned for modification 2 June 2008/ Accepted 8 July 2008

We have previously shown that deficiency of the methyl binding domain protein Mbd2 dramatically reduces adenoma burden on an ApcMin/+ background. To investigate the mechanism underlying this phenomenon, we have determined the effect of Mbd2 deficiency upon the phenotypes imposed by the conditional deletion of Apc in the small intestine. Microarray analysis demonstrated a partial suppression of the Wnt pathway in the absence of Mbd2. Mbd2 deficiency also influenced one immediate cellular consequence of Apc loss, with normalization of Paneth cell positioning. From a mechanistic perspective, we show that deficiency of Mbd2 elevates levels of the known Wnt target Lect2, and we confirm here that Mbd2 binds the Lect2 promoter in association with NuRD. Furthermore, we show that Lect2 is capable of functioning as a Wnt pathway repressor. These results therefore provide a mechanistic basis for the epigenetic control of adenoma formation mediated through Mbd2.


* Corresponding author. Mailing address: Cardiff School of Biosciences, Cardiff University, Cardiff CF10 3US, United Kingdom. Phone: 011-44-02920 874609. Fax: 011-44-02920 874116. E-mail: clarkear{at}cf.ac.uk

{triangledown} Published ahead of print on 21 July 2008.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.

{ddagger} Present address: Ludwig Institute for Cancer Research, PO Royal Melbourne Hospital, Melbourne, VIC 3050, Australia.


Molecular and Cellular Biology, October 2008, p. 6094-6103, Vol. 28, No. 19
0270-7306/08/$08.00+0     doi:10.1128/MCB.00539-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Lukas, J., Mazna, P., Valenta, T., Doubravska, L., Pospichalova, V., Vojtechova, M., Fafilek, B., Ivanek, R., Plachy, J., Novak, J., Korinek, V. (2009). Dazap2 modulates transcription driven by the Wnt effector TCF-4. Nucleic Acids Res 37: 3007-3020 [Abstract] [Full Text]