bioRxivCell Biology
Matrix metalloproteinase-2 mediates ribosomal RNA transcription by cleaving nucleolar histones
M. A. M. Ali, J. A. Garcia-Vilas, C. R. Cromwell, B. P. Hubbard, M. J. Hendzel, R. Schulz
Abstract
Cell proliferation and survival require continuous ribosome biogenesis and protein synthesis. Genes encoding ribosomal RNA (rRNA) are physically located in a specialized substructure within the nucleus known as the nucleolus, which has a central role in the biogenesis of ribosomes. Matrix metalloproteinase-2 (MMP-2) was previously detected in the nucleus. However, its role there is elusive. Herein we report that MMP-2 resides within the nucleolus to regulate rRNA transcription. MMP-2 is enriched at the promoter region of rRNA gene repeats and its inhibition downregulates pre-rRNA transcription. The N-terminal tail of histone H3 is clipped by MMP-2 in the nucleolus and is associated with increased rRNA transcription. Knocking down/out MMP-2 or inhibiting its activity prevents histone H3 cleavage and reduces both rRNA transcription and cell proliferation. In addition to the known extracellular roles of MMP-2 in tumor growth, our data reveal an epigenetic mechanism whereby intranucleolar MMP-2 regulates cell proliferation through histone proteolysis and facilitation of rRNA transcription.
- organism: human
- assay: DNA methylation
- assay: proteomics
- research focus: cell type annotation
- research focus: chromatin & epigenetic regulation
- research focus: cell signaling & trafficking
- approach: experimental assay
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