Primate-Specific ORF0 Contributes to Retrotransposon-Mediated Diversity

Authors
Ahmet M. Denli1, Iñigo Narvaiza1, Bilal E. Kerman1, Monique Pena1, Christopher Benner1, Maria C.N. Marchetto1, Jolene K. Diedrich5, Aaron Aslanian2, Jiao Ma3, 6, James J. Moresco5, Lynne Moore1, Tony Hunter2, 4, Alan Saghatelian3, Fred H. Gage1, 7, 8.
02-10-2016
12:00pm
PST
Categories
Interconnected RNA Processes
Speaker
Boris Reznik
Abstract
LINE-1 retrotransposons are fast-evolving mobile genetic entities that play roles in gene regulation, pathological conditions, and evolution. Here, we show that the primate LINE-1 50 UTR contains a primate-specific open reading frame (ORF) in the antisense orientation that we named ORF0. The gene product of this ORF localizes to promyelocytic leukemia-adjacent nuclear bodies. ORF0 is present in more than 3,000 loci across human and chimpanzee genomes and has a promoter and a conserved strong Kozak sequence that supports translation. By virtue of containing two splice donor sites, ORF0 can also form fusion proteins with proximal exons. ORF0 transcripts are readily detected in induced pluripotent stem (iPS) cells from both primate species. Capped and polyadenylated ORF0 mRNAs are present in the cytoplasm, and endogenous ORF0 peptides are identified upon proteomic analysis. Finally, ORF0 enhances LINE-1 mobility. Taken together, these results suggest a role for ORF0 in retrotransposon-mediated diversity.