Journal article
Kaiso Directs the Transcriptional Corepressor MTG16 to the Kaiso Binding Site in Target Promoters
PloS one, Vol.7(12), pp.e51205-e51205
12/12/2012
DOI: 10.1371/journal.pone.0051205
PMCID: PMC3521008
PMID: 23251453
Abstract
Myeloid translocation genes (MTGs) are transcriptional corepressors originally identified in acute myelogenous leukemia that have recently been linked to epithelial malignancy with non-synonymous mutations identified in both MTG8 and MTG16 in colon, breast, and lung carcinoma in addition to functioning as negative regulators of WNT and Notch signaling. A yeast two-hybrid approach was used to discover novel MTG binding partners. This screen identified the Zinc fingers, C2H2 and BTB domain containing (ZBTB) family members ZBTB4 and ZBTB38 as MTG16 interacting proteins. ZBTB4 is downregulated in breast cancer and modulates p53 responses. Because ZBTB33 (Kaiso), like MTG16, modulates Wnt signaling at the level of TCF4, and its deletion suppresses intestinal tumorigenesis in the Apc(Min) mouse, we determined that Kaiso also interacted with MTG16 to modulate transcription. The zinc finger domains of Kaiso as well as ZBTB4 and ZBTB38 bound MTG16 and the association with Kaiso was confirmed using co-immunoprecipitation. MTG family members were required to efficiently repress both a heterologous reporter construct containing Kaiso binding sites (4xKBS) and the known Kaiso target, Matrix metalloproteinase-7 (MMP-7/Matrilysin). Moreover, chromatin immunoprecipitation studies placed MTG16 in a complex occupying the Kaiso binding site on the MMP-7 promoter. The presence of MTG16 in this complex, and its contributions to transcriptional repression both required Kaiso binding to its binding site on DNA, establishing MTG16-Kaiso binding as functionally relevant in Kaiso-dependent transcriptional repression. Examination of a large multi-stage CRC expression array dataset revealed patterns of Kaiso, MTG16, and MMP-7 expression supporting the hypothesis that loss of either Kaiso or MTG16 can de-regulate a target promoter such as that of MMP-7. These findings provide new insights into the mechanisms of transcriptional control by ZBTB family members and broaden the scope of co-repressor functions for the MTG family, suggesting coordinate regulation of transcription by Kaiso/MTG complexes in cancer.
Details
- Title: Subtitle
- Kaiso Directs the Transcriptional Corepressor MTG16 to the Kaiso Binding Site in Target Promoters
- Creators
- Caitlyn W. Barrett - Vanderbilt University Medical CenterJ. Joshua Smith - Vanderbilt UniversityLauren C. Lu - Vanderbilt UniversityNicholas Markham - Vanderbilt University Medical CenterKristy R. Stengel - Vanderbilt University Medical CenterSarah P. Short - Vanderbilt University Medical CenterBaolin Zhang - Vanderbilt UniversityAubrey A. Hunt - Vanderbilt University Medical CenterBarbara M. Fingleton - Vanderbilt UniversityRobert H. Carnahan - Vanderbilt UniversityMichael E. Engel - University of UtahXi Chen - Vanderbilt UniversityR. Daniel Beauchamp - Vanderbilt UniversityKeith T. Wilson - Vanderbilt University Medical CenterScott W. Hiebert - Vanderbilt UniversityAlbert B. Reynolds - Vanderbilt UniversityChristopher S. Williams - Vanderbilt University Medical Center
- Resource Type
- Journal article
- Publication Details
- PloS one, Vol.7(12), pp.e51205-e51205
- DOI
- 10.1371/journal.pone.0051205
- PMID
- 23251453
- PMCID
- PMC3521008
- NLM abbreviation
- PLoS One
- ISSN
- 1932-6203
- eISSN
- 1932-6203
- Publisher
- Public Library Science
- Number of pages
- 13
- Grant note
- UL1RR024975 / NATIONAL CENTER FOR RESEARCH RESOURCES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Center for Research Resources (NCRR) 2 UL1 TR000445-06 / National Center for Advancing Translational Sciences; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Center for Advancing Translational Sciences (NCATS) Veterans Administration; US Department of Veterans Affairs UL1TR000445 / NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Center for Advancing Translational Sciences (NCATS) P30DK058404 / NIH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA 1F31CA167920 / NCI sponsored fellowship; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI) P30DK058404 / NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK) R01AT004821 / National Center for Complementary & Integrative Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA I01BX001453 / Veterans Affairs; US Department of Veterans Affairs UL1 RR024975-01 / National Center for Research Resources; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Center for Research Resources (NCRR) K-08 (5K08DK080221) / NIDDK; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK) P30CA068485 / Vanderbilt Ingram Cancer Center shared resources P30CA068485 / NATIONAL CANCER INSTITUTE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI) T32GM008554 / NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of General Medical Sciences (NIGMS) NIH T32 GM08554 / Cellular and Biochemical and Molecular Sciences Training Program 116552 / American Cancer Society ACS-RSG; American Cancer Society
- Language
- English
- Date published
- 12/12/2012
- Academic Unit
- Hematology, Oncology, and Blood & Marrow Transplantation; Internal Medicine
- Record Identifier
- 9984420943902771
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