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"MSH2 is also phosphorylated by NPM-ALK at tyrosine 238 by oncogenic fusion protein NPM-ALK, leading to impaired MMR in anaplastic large cell lymphoma.24 Histone deacetylase 6 (HDAC6) and HDAC10 were found to separately deacetylate MSH2 at distinct sites of its C-terminus and N-terminus, which increases MSH2 ubiquitination and degradation and ultimately reduces DNA MMR activities.25 26 Conversely, ubiquitin-specific peptidase 10 (USP10) deubiquitinates MSH2 and compromises DNA damage response and MMR activity.27Protein arginine methyltransferases (PRMTs) are a family of enzymes that catalyze protein arginine methylation."
"Here we report that ubiquitin-specific peptidase 10 (<span class="match term0">USP10</span>) interacts with and stabilizes <span class="match term1">MSH2</span>"