Complex interactomes and post-translational modifications of the regulatory proteins HABP4 and SERBP1 suggest pleiotropic cellular functions
| Autor: | Ângela Saito, Flávia Regina Moraes da Silva, Talita Diniz Melo-Hanchuk, Jörg Kobarg, Carolina Colleti |
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| Rok vydání: | 2019 |
| Předmět: |
0301 basic medicine
Regulation of gene expression Messenger RNA Cell signaling SUMO protein Protein interactions Review Biology Interactome Cell biology Protein–protein interaction 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Regulatory protein 030220 oncology & carcinogenesis RNA splicing Transcriptional regulation Cellular localization Cancer Post-translational modifications |
| Zdroj: | World Journal of Biological Chemistry |
| ISSN: | 1949-8454 |
| Popis: | The 57 kDa antigen recognized by the Ki-1 antibody, is also known as intracellular hyaluronic acid binding protein 4 and shares 40.7% identity and 67.4% similarity with serpin mRNA binding protein 1, which is also named CGI-55, or plasminogen activator inhibitor type-1-RNA binding protein-1, indicating that they might be paralog proteins, possibly with similar or redundant functions in human cells. Through the identification of their protein interactomes, both regulatory proteins have been functionally implicated in transcriptional regulation, mRNA metabolism, specifically RNA splicing, the regulation of mRNA stability, especially, in the context of the progesterone hormone response, and the DNA damage response. Both proteins also show a complex pattern of post-translational modifications, involving Ser/Thr phosphorylation, mainly through protein kinase C, arginine methylation and SUMOylation, suggesting that their functions and locations are highly regulated. Furthermore, they show a highly dynamic cellular localization pattern with localizations in both the cytoplasm and nucleus as well as punctuated localizations in both granular cytoplasmic protein bodies, upon stress, and nuclear splicing speckles. Several reports in the literature show altered expressions of both regulatory proteins in a series of cancers as well as mutations in their genes that may contribute to tumorigenesis. This review highlights important aspects of the structure, interactome, post-translational modifications, sub-cellular localization and function of both regulatory proteins and further discusses their possible functions and their potential as tumor markers in different cancer settings. |
| Databáze: | OpenAIRE |
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