| Literature DB >> 32286153 |
Hagen Schwenzer1, Mai Abdel Mouti1, Pia Neubert1, Josephine Morris1, Joanne Stockton2, Sarah Bonham3, Martin Fellermeyer1, James Chettle1, Roman Fischer3, Andrew D Beggs2, Sarah P Blagden1.
Abstract
LARP1 is an oncogenic RNA-binding protein required for ribosome biogenesis and cancer cell survival. From published in vitro studies, there is disparity over which of two different LARP1 protein isoforms (termed the long LI-LARP1 and short SI-LARP1) is the canonical. Here, after conducting a series of biochemical and cellular assays, we conclude that LI-LARP1 (NM_033551.3 > NP_056130.2) is the dominantly expressed form. We observe that SI-LARP1 (NM_015315.5> NP_056130.2) is epigenetically repressed and that this repression is evolutionarily conserved in all but a small subclade of mammalian species. As with other LARP family members, there are multiple potential LARP1 mRNA isoforms that appear to be censored within the nucleus. The capacity of the cell to modulate splicing and expression of these apparently 'redundant' mRNAs hints at contextually specific mechanisms of LARP1 expression.Entities:
Keywords: LARP1; RNA Binding Proteins; alternative protein isoforms; cancer
Year: 2020 PMID: 32286153 PMCID: PMC7928056 DOI: 10.1080/15476286.2020.1744320
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652