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Detalle de: Cystatin D locates in the nucleus at sites of active transcription and modulates gene and protein expression

Title Cystatin D locates in the nucleus at sites of active transcription and modulates gene and protein expression
Abstract

Cystatin D is an inhibitor of lysosomal and secreted cysteine proteases. Strikingly, cystatin D has been found to inhibit proliferation, migration, and invasion of colon carcinoma cells indicating tumor suppressor activity that is unrelated to protease inhibition. Here, we demonstrate that a proportion of cystatin D locates within the cell nucleus at specific transcriptionally active chromatin sites. Consistently, transcriptomic analysis show that cystatin D alters gene expression, including that of genes encoding transcription factors such as RUNX1, RUNX2, and MEF2C in HCT116 cells. In concordance with transcriptomic data, quantitative proteomic analysis identified 292 proteins differentially expressed in cystatin D-expressing cells involved in cell adhesion, cytoskeleton, and RNA synthesis and processing. Furthermore, using cytokine arrays we found that cystatin D reduces the secretion of several protumor cytokines such as fibroblast growth factor-4, CX3CL1/fractalkine, neurotrophin 4 oncostatin-M, pulmonary and activation-regulated chemokine/CCL18, and transforming growth factor B3. These results support an unanticipated role of cystatin D in the cell nucleus, controlling the transcription of specific genes involved in crucial cellular functions, which may mediate its protective action in colon cancer.

Apa Reference Ferrer-Mayorga, G., Alvarez-Díaz, S., Valle, N., De Las Rivas, J., Mendes, M., Barderas, R., Canals, F., Tapia, O., Casal, J. I., Lafarga, M., & Muñoz, A. (2015). Cystatin D Locates in the Nucleus at Sites of Active Transcription and Modulates Gene and Protein Expression. Journal of Biological Chemistry, 290(44), 26533–26548. 10.1074/jbc.m115.660175
Doi 10.1074/jbc.M115.660175
Publication Date Oct 2015
Publication Type Article
Researcher Javier De Las Rivas
Ontology Transcriptomics, Expression Profiling, Regulatory biology, Proteomics, Drug Discovery and design, Behavioral Ecology
Research Groups Bioinformatics and Functional Genomics
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