bioRxivCancer BiologyPreprint
The PTPRT pseudo-phosphatase domain is a denitrase
Yiqing ZhaoiD, Shuliang Zhao, Yujun Hao, Benlian Wang, Peng Zhang, Xiujing Feng, Yicheng Chen, Jing Song, John Mieyal, Sanford Markowitz, Rob M. Ewing, Ronald A. Conlon, Masaru Miyagi, Zhenghe WangiD
Abstract
Protein tyrosine nitration occurs under both physiological and pathological conditions1. However, enzymes that remove this protein modification have not yet been identified. Here we report that the pseudo-phosphatase domain of protein tyrosine receptor T (PTPRT) is a denitrase that removes nitro-groups from tyrosine residues in paxillin. PTPRT normally functions as a tumor suppressor and is frequently mutated in a variety of human cancers including colorectal cancer2,3. We demonstrate that some of the tumor-derived mutations located in the pseudophosphatase domain impair the denitrase activity. Moreover, PTPRT mutant mice that inactivate the denitrase activity are susceptible to carcinogen-induced colon tumor formation. This study uncovers a novel enzymatic activity that is involved in tumor suppression.
- organism: mouse
- organism: human
- assay: proteomics
- research focus: cancer & tumor microenvironment
- approach: experimental assay
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