Primate-specific ORF0 contributes to retrotransposon-mediated diversity
- PMID: 26496605
- DOI: 10.1016/j.cell.2015.09.025
Primate-specific ORF0 contributes to retrotransposon-mediated diversity
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 5'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.
Copyright © 2015 Elsevier Inc. All rights reserved.
Comment in
-
Much ado about zero.Cell. 2015 Oct 22;163(3):534-5. doi: 10.1016/j.cell.2015.10.033. Epub 2015 Oct 22. Cell. 2015. PMID: 26496595
Similar articles
-
Efficient translation initiation directed by the 900-nucleotide-long and GC-rich 5' untranslated region of the human retrotransposon LINE-1 mRNA is strictly cap dependent rather than internal ribosome entry site mediated.Mol Cell Biol. 2007 Jul;27(13):4685-97. doi: 10.1128/MCB.02138-06. Epub 2007 Apr 30. Mol Cell Biol. 2007. PMID: 17470553 Free PMC article.
-
Much ado about zero.Cell. 2015 Oct 22;163(3):534-5. doi: 10.1016/j.cell.2015.10.033. Epub 2015 Oct 22. Cell. 2015. PMID: 26496595
-
Analysis of full length ADAMTS6 transcript reveals alternative splicing and a role for the 5' untranslated region in translational control.Gene. 2005 Oct 10;359:99-110. doi: 10.1016/j.gene.2005.06.011. Gene. 2005. PMID: 16129570
-
A LINE element from the pufferfish (fugu) Fugu rubripes which shows similarity to the CR1 family of non-LTR retrotransposons.Gene. 1999 Feb 18;227(2):169-79. doi: 10.1016/s0378-1119(98)00600-3. Gene. 1999. PMID: 10023050
-
Some like it translated: small ORFs in the 5'UTR.Exp Cell Res. 2020 Nov 1;396(1):112229. doi: 10.1016/j.yexcr.2020.112229. Epub 2020 Aug 17. Exp Cell Res. 2020. PMID: 32818479 Review.
Cited by
-
Retrotransposons as regulators of gene expression.Science. 2016 Feb 12;351(6274):aac7247. doi: 10.1126/science.aac7247. Epub 2016 Feb 11. Science. 2016. PMID: 26912865 Free PMC article. Review.
-
Transposable elements in cancer.Nat Rev Cancer. 2017 Jul;17(7):415-424. doi: 10.1038/nrc.2017.35. Epub 2017 Jun 9. Nat Rev Cancer. 2017. PMID: 28642606 Review.
-
Transposable Elements, Inflammation, and Neurological Disease.Front Neurol. 2019 Aug 20;10:894. doi: 10.3389/fneur.2019.00894. eCollection 2019. Front Neurol. 2019. PMID: 31481926 Free PMC article. Review.
-
miR-128 Restriction of LINE-1 (L1) Retrotransposition Is Dependent on Targeting hnRNPA1 mRNA.Int J Mol Sci. 2019 Apr 21;20(8):1955. doi: 10.3390/ijms20081955. Int J Mol Sci. 2019. PMID: 31010097 Free PMC article.
-
Frequency and mechanisms of LINE-1 retrotransposon insertions at CRISPR/Cas9 sites.Nat Commun. 2022 Jun 27;13(1):3685. doi: 10.1038/s41467-022-31322-3. Nat Commun. 2022. PMID: 35760782 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources