| Literature DB >> 30176153 |
Sharad Awasthi1, Baskar Chakrapani1, Arun Mahesh1, Pavithra L Chavali2, Sreenivas Chavali2, Arunkumar Dhayalan1.
Abstract
DDX39B, a DExD RNA helicase, is known to be involved in various cellular processes such as mRNA export, splicing and translation. Previous studies showed that the overexpression of DDX39B promotes the global translation but inhibits the mRNA export in a dominant negative manner. This presents a conundrum as to how DDX39B overexpression would increase the global translation if it inhibits the nuclear export of mRNAs. We resolve this by showing that DDX39B affects the levels of pre-ribosomal RNA by regulating its stability as well as synthesis. Furthermore, DDX39B promotes proliferation and colony forming potential of cells and its levels are significantly elevated in diverse cancer types. Thus, increase in DDX39B enhances global translation and cell proliferation through upregulation of pre-ribosomal RNA. This highlights a possible mechanism by which dysregulation of DDX39B expression could lead to oncogenesis.Entities:
Keywords: RNA helicase; cancers; clonogenic capacity; pre-ribosomal RNA; translation
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Year: 2018 PMID: 30176153 PMCID: PMC6284572 DOI: 10.1080/15476286.2018.1517011
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652