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Mol Cell Biol ; 35(24): 4199-211, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26438601

ABSTRACT

The lysine (K)-specific demethylase (LSD1) family of histone demethylases regulates chromatin structure and the transcriptional potential of genes. LSD1 is frequently deregulated in tumors, and depletion of LSD1 family members causes developmental defects. Here, we report that reductions in the expression of the Pumilio (PUM) translational repressor complex enhanced phenotypes due to dLsd1 depletion in Drosophila. We show that the PUM complex is a target of LSD1 regulation in fly and mammalian cells and that its expression is inversely correlated with LSD1 levels in human bladder carcinoma. Unexpectedly, we find that PUM posttranscriptionally regulates LSD1 family protein levels in flies and human cells, indicating the existence of feedback loops between the LSD1 family and the PUM complex. Our results highlight a new posttranscriptional mechanism regulating LSD1 activity and suggest that the feedback loop between the LSD1 family and the PUM complex may be functionally important during development and in human malignancies.


Subject(s)
Drosophila Proteins/metabolism , Feedback, Physiological , Oxidoreductases, N-Demethylating/metabolism , RNA-Binding Proteins/metabolism , Animals , Cell Line, Tumor , DNA-Binding Proteins/biosynthesis , Drosophila , Drosophila Proteins/biosynthesis , HeLa Cells , Histone Demethylases/metabolism , Humans , MCF-7 Cells , Mice , RNA Interference , RNA Processing, Post-Transcriptional , RNA, Messenger/genetics , RNA, Small Interfering , RNA-Binding Proteins/biosynthesis , Urinary Bladder Neoplasms/pathology
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