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De Novo Generation of Somatic Stem Cells by YAP/TAZ
Published on: May 7, 2018
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DNA binding partners of YAP/TAZ
Min-Kyu Kim1, Ju-Won Jang1, Suk-Chul Bae1
1Department of Biochemistry, College of Medicine, and Institute for Tumor Research, Chungbuk National University, Cheongju 28644, Korea.
BMB Reports
|January 26, 2018
Summary
The Hippo pathway regulates organ size and cancer by controlling YAP/TAZ proteins. YAP
Area of Science:
- Cell Biology
- Molecular Biology
- Cancer Research
Background:
- The Hippo signaling pathway is crucial for maintaining tissue homeostasis and organ size.
- It regulates the activity of transcriptional coactivators YES-associated protein (YAP) and PDZ-binding protein TAZ.
- Hippo signaling interacts with other pathways like WNT, BMPs, Notch, GPCRs, and Hedgehog.
Purpose of the Study:
- To summarize the roles of YAP based on its DNA-binding partners.
- To discuss the context-dependent functions of YAP and TAZ.
- To explore YAP's dual role as an oncogene or tumor suppressor.
Main Methods:
- Review of existing literature on Hippo signaling and YAP/TAZ.
- Analysis of YAP's interactions with various DNA-binding proteins.
- Discussion of experimental evidence supporting YAP's context-dependent functions.
Main Results:
- YAP and TAZ require DNA-binding partners to regulate gene expression.
- TEAD family members are key YAP/TAZ partners, often promoting proliferation (oncogenic role).
- YAP can also bind tumor suppressors like RUNXs and p73, suggesting a tumor-suppressive role.
Conclusions:
- YAP's function as an oncogene or tumor suppressor is determined by its binding partners.
- The context-dependent activity of YAP/TAZ is critical for understanding their roles in health and disease.
- Further research into YAP's interactions can reveal new therapeutic strategies for cancer.
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