Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 902

The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.

Expression of Linear and Novel Circular Forms of an INK4/ARF-Associated Non-Coding RNA Correlates with Atherosclerosis Risk

Open access
Burd, Christin E., Jeck, William R., Liu, Yan, Sanoff, Hanna K., Wang, Zefeng, Sharpless, Norman E.·2010·PLoS Genetics

Abstract

Human genome-wide association studies have linked single nucleotide polymorphisms (SNPs) on chromosome 9p21.3 near the INK4/ARF (CDKN2a/b) locus with susceptibility to atherosclerotic vascular disease (ASVD). Although this locus encodes three well-characterized tumor suppressors, p16(INK4a), p15(INK4b), and ARF, the SNPs most strongly associated with ASVD are ∼120 kb from the nearest coding gene within a long non-coding RNA (ncRNA) known as ANRIL (CDKN2BAS). While individuals homozygous for the atherosclerotic risk allele show decreased expression of ANRIL and the coding INK4/ARF transcripts, the mechanism by which such distant genetic variants influence INK4/ARF expression is unknown. Here, using rapid amplification of cDNA ends (RACE) and analysis of next-generation RNA sequencing datasets, we determined the structure and abundance of multiple ANRIL species. Each of these species was present at very low copy numbers in primary and cultured cells; however, only the expression of ANRIL isoforms containing exons proximal to the INK4/ARF locus correlated with the ASVD risk alleles. Surprisingly, RACE also identified transcripts containing non-colinear ANRIL exonic sequences, whose expression also correlated with genotype and INK4/ARF expression. These non-polyadenylated RNAs resisted RNAse R digestion and could be PCR amplified using outward-facing primers, suggesting they represent circular RNA structures that could arise from by-products of mRNA splicing. Next-generation DNA sequencing and splice prediction algorithms identified polymorphisms within the ASVD risk interval that may regulate ANRIL splicing and circular ANRIL (cANRIL) production. These results identify novel circular RNA products emanating from the ANRIL locus and suggest causal variants at 9p21.3 regulate INK4/ARF expression and ASVD risk by modulating ANRIL expression and/or structure.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1371/journal.pgen.1001233

Cites

20 of 20 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

1 retracted

Show all 20 references

Research works printed but not linked: 61

  1. E Biros, 2010, Association of an allele on chromosome 9 and abdominal aortic aneurysm., Atherosclerosis
  2. MJ Bown, 2008, Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm., Circ Cardiovasc Genet, 1, 39, 10.1161/CIRCGENETICS.108.789727 · DOI
  3. AR Thompson, 2009, Sequence variant on 9p21 is associated with the presence of abdominal aortic aneurysm disease but does not have an impact on aneurysmal expansion., Eur J Hum Genet, 17, 391, 10.1038/ejhg.2008.196 · DOI
  4. A Helgadottir, 2008, The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm., Nat Genet, 40, 217, 10.1038/ng.72 · DOI · Paper page
  5. M Matarin, 2008, Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21., Stroke, 39, 1586, 10.1161/STROKEAHA.107.502963 · DOI · Paper page
  6. A Gschwendtner, 2009, Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke., Ann Neurol, 65, 531, 10.1002/ana.21590 · DOI
  7. JG Smith, 2009, Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study., Circ Cardiovasc Genet, 2, 159, 10.1161/CIRCGENETICS.108.835173 · DOI
  8. C Cluett, 2009, The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people., Circ Cardiovasc Genet, 2, 347, 10.1161/CIRCGENETICS.108.825935 · DOI
  9. S Ye, 2008, Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study., J Am Coll Cardiol, 52, 378, 10.1016/j.jacc.2007.11.087 · DOI
  10. HM Broadbent, 2008, Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p., Hum Mol Genet, 17, 806, 10.1093/hmg/ddm352 · DOI · Paper page
  11. SB Seidelmann, 2008, Athsq1 is an atherosclerosis modifier locus with dramatic effects on lesion area and prominent accumulation of versican., Arterioscler Thromb Vasc Biol, 28, 2180, 10.1161/ATVBAHA.108.176800 · DOI
  12. R Wessely, 2010, Atherosclerosis and cell cycle: put the brakes on! Critical role for cyclin-dependent kinase inhibitors., J Am Coll Cardiol, 55, 2269, 10.1016/j.jacc.2010.02.017 · DOI
  13. M Boehm, 2003, The cell cycle and cardiovascular diseases., Prog Cell Cycle Res, 5, 19
  14. F Gizard, 2005, PPAR alpha inhibits vascular smooth muscle cell proliferation underlying intimal hyperplasia by inducing the tumor suppressor p16INK4a., J Clin Invest, 115, 3228, 10.1172/JCI22756 · DOI
  15. H Gonzalez-Navarro, 2010, p19(ARF) deficiency reduces macrophage and vascular smooth muscle cell apoptosis and aggravates atherosclerosis., J Am Coll Cardiol, 55, 2258, 10.1016/j.jacc.2010.01.026 · DOI
  16. N Kalinina, 2004, Smad expression in human atherosclerotic lesions: evidence for impaired TGF-beta/Smad signaling in smooth muscle cells of fibrofatty lesions., Arterioscler Thromb Vasc Biol, 24, 1391, 10.1161/01.ATV.0000133605.89421.79 · DOI
  17. I Reynisdottir, 1995, Kip/Cip and Ink4 Cdk inhibitors cooperate to induce cell cycle arrest in response to TGF-beta., Genes Dev, 9, 1831, 10.1101/gad.9.15.1831 · DOI · Paper page
  18. DJ Grainger, 2004, Transforming growth factor beta and atherosclerosis: so far, so good for the protective cytokine hypothesis., Arterioscler Thromb Vasc Biol, 24, 399, 10.1161/01.ATV.0000114567.76772.33 · DOI · Paper page
  19. L Yvan-Charvet, 2010, ATP-binding cassette transporters and HDL suppress hematopoietic stem cell proliferation., Science, 328, 1689, 10.1126/science.1189731 · DOI · Paper page
  20. A Visel, 2010, Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice., Nature, 464, 409, 10.1038/nature08801 · DOI · Paper page
  21. E Pasmant, 2007, Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF., Cancer Res, 67, 3963, 10.1158/0008-5472.CAN-06-2004 · DOI · Paper page
  22. L Folkersen, 2009, Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants., PLoS One, 4, e7677, 10.1371/journal.pone.0007677 · DOI · Paper page
  23. T Kyriakou, 2009, ANRIL, The non-coding RNA present in the chromosome 9 CAD associated locus, has multiple splice variants and a potential regulatory role in CDKN2B expression., Atherosclerosis, 207, e3, 10.1016/j.atherosclerosis.2009.09.036 · doi:10.1016/j.atherosclerosis.2009.09.036
  24. O Jarinova, 2009, Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus., Arterioscler Thromb Vasc Biol, 29, 1671, 10.1161/ATVBAHA.109.189522 · DOI · Paper page
  25. S Dhawan, 2009, Bmi-1 regulates the Ink4a/Arf locus to control pancreatic beta-cell proliferation., Genes Dev, 23, 906, 10.1101/gad.1742609 · DOI · Paper page
  26. H Chen, 2009, Polycomb protein Ezh2 regulates pancreatic beta-cell Ink4a/Arf expression and regeneration in diabetes mellitus., Genes Dev, 23, 975, 10.1101/gad.1742509 · DOI · Paper page
  27. Y Kotake, 2007, pRB family proteins are required for H3K27 trimethylation and Polycomb repression complexes binding to and silencing p16INK4alpha tumor suppressor gene., Genes Dev, 21, 49, 10.1101/gad.1499407 · DOI · Paper page
  28. R Terranova, 2008, Polycomb group proteins Ezh2 and Rnf2 direct genomic contraction and imprinted repression in early mouse embryos., Dev Cell, 15, 668, 10.1016/j.devcel.2008.08.015 · DOI · Paper page
  29. JL Rinn, 2007, Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs., Cell, 129, 1311, 10.1016/j.cell.2007.05.022 · DOI · Paper page
  30. J Zhao, 2008, Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome., Science, 322, 750, 10.1126/science.1163045 · DOI · Paper page
  31. RR Pandey, 2008, Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation., Mol Cell, 32, 232, 10.1016/j.molcel.2008.08.022 · DOI · Paper page
  32. RA Gupta, 2010, Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis., Nature, 464, 1071, 10.1038/nature08975 · DOI · Paper page
  33. Y Liu, 2009, Expression of p16(INK4a) in peripheral blood T-cells is a biomarker of human aging., Aging Cell, 8, 439, 10.1111/j.1474-9726.2009.00489.x · DOI · Paper page
  34. E Hara, 1996, Regulation of p16CDKN2 expression and its implications for cell immortalization and senescence., Mol Cell Biol, 16, 859, 10.1128/MCB.16.3.859 · DOI · Paper page
  35. KF Au, 2010, Detection of splice junctions from paired-end RNA-seq data by SpliceMap., Nucleic Acids Res
  36. GP Nielsen, 1999, Immunohistochemical survey of p16INK4A expression in normal human adult and infant tissues., Lab Invest, 79, 1137
  37. M Schmid, 2000, A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer., Oncogene, 19, 5747, 10.1038/sj.onc.1203942 · DOI
  38. K Chen, 2009, BreakDancer: an algorithm for high-resolution mapping of genomic structural variation., Nat Methods, 6, 677, 10.1038/nmeth.1363 · DOI · Paper page
  39. PG Zaphiropoulos, 1996, Circular RNAs from transcripts of the rat cytochrome P450 2C24 gene: correlation with exon skipping., Proc Natl Acad Sci U S A, 93, 6536, 10.1073/pnas.93.13.6536 · DOI · Paper page
  40. H Suzuki, 2006, Characterization of RNase R-digested cellular RNA source that consists of lariat and circular RNAs from pre-mRNA splicing., Nucleic Acids Res, 34, e63, 10.1093/nar/gkl151 · DOI · Paper page
  41. RJ Dixon, 2005, A genome-wide survey demonstrates widespread non-linear mRNA in expressed sequences from multiple species., Nucleic Acids Res, 33, 5904, 10.1093/nar/gki893 · DOI
  42. Z Wang, 2004, Systematic identification and analysis of exonic splicing silencers., Cell, 119, 831, 10.1016/j.cell.2004.11.010 · DOI · Paper page
  43. WG Fairbrother, 2002, Predictive identification of exonic splicing enhancers in human genes., Science, 297, 1007, 10.1126/science.1073774 · DOI · Paper page
  44. Z Wang, 2008, Splicing regulation: from a parts list of regulatory elements to an integrated splicing code., Rna, 14, 802, 10.1261/rna.876308 · DOI · Paper page
  45. JM Nigro, 1991, Scrambled exons., Cell, 64, 607, 10.1016/0092-8674(91)90244-S · DOI · Paper page
  46. LM Holdt, 2010, ANRIL expression is associated with atherosclerosis risk at chromosome 9p21., Arterioscler Thromb Vasc Biol, 30, 620, 10.1161/ATVBAHA.109.196832 · DOI · Paper page
  47. MS Cunnington, 2010, Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression., PLoS Genet, 6, e1000899, 10.1371/journal.pgen.1000899 · DOI · Paper page
  48. SE Messaoudi-Aubert, 2010, Role for the MOV10 RNA helicase in polycomb-mediated repression of the INK4a tumor suppressor., Nat Struct Mol Biol, 17, 862, 10.1038/nsmb.1824 · DOI
  49. D Mancini-Dinardo, 2006, Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes., Genes Dev, 20, 1268, 10.1101/gad.1416906 · DOI · Paper page
  50. C Kanduri, 2006, The length of the transcript encoded from the Kcnq1ot1 antisense promoter determines the degree of silencing., Embo J, 25, 2096, 10.1038/sj.emboj.7601090 · DOI
  51. RJ Dixon, 2007, Complementary intron sequence motifs associated with human exon repetition: a role for intragenic, inter-transcript interactions in gene expression., Bioinformatics, 23, 150, 10.1093/bioinformatics/btl575 · doi:10.1093/bioinformatics/btl575
  52. C Cocquerelle, 1992, Splicing with inverted order of exons occurs proximal to large introns., Embo J, 11, 1095, 10.1002/j.1460-2075.1992.tb05148.x · DOI · Paper page
  53. L Bonen, 2001, The ins and outs of group II introns., Trends Genet, 17, 322, 10.1016/S0168-9525(01)02324-1 · DOI · Paper page
  54. A Kos, 1986, The hepatitis delta (delta) virus possesses a circular RNA., Nature, 323, 558, 10.1038/323558a0 · DOI · Paper page
  55. EM Tsagris, 2008, Viroids., Cell Microbiol, 10, 2168, 10.1111/j.1462-5822.2008.01231.x · DOI
  56. S Shete, 2009, Genome-wide association study identifies five susceptibility loci for glioma., Nat Genet, 41, 899, 10.1038/ng.407 · DOI · Paper page
  57. M Wrensch, 2009, Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility., Nat Genet, 41, 905, 10.1038/ng.408 · DOI · Paper page
  58. JX Bei, 2010, A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci., Nat Genet, 42, 599, 10.1038/ng.601 · DOI · Paper page
  59. E Emanuele, 2010, Preliminary evidence of a genetic association between chromosome 9p21.3 and human longevity., Rejuvenation Res, 13, 23, 10.1089/rej.2009.0970 · DOI
  60. AB Hanker, 2008, Tools to study the function of the Ras-related, estrogen-regulated growth inhibitor in breast cancer., Methods Enzymol, 439, 53, 10.1016/S0076-6879(07)00405-3 · doi:10.1016/s0076-6879(07)00405-3
  61. JM Shields, 2007, Lack of extracellular signal-regulated kinase mitogen-activated protein kinase signaling shows a new type of melanoma., Cancer Res, 67, 1502, 10.1158/0008-5472.CAN-06-3311 · DOI

Cited by

See all 902

Metadata

Authors
Burd, C. E., Jeck, W. R., Liu, Y., Sanoff, H. K., Wang, Z., & Sharpless, N. E.
Venue
PLoS Genetics
Published
2010-12-02
Volume
6
Issue
12
Pages
e1001233
ISSN
  • 1553-7390 (ISSN-L)
  • 1553-7404
OpenAlex
W1975909559
Cited by
902
References
20
FWCI
6.50
Type
journal article
Language
en
Open access
gold

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Expression of Linear and Novel Circular Forms of an INK4/ARF-Associated Non-Coding RNA Correlates with Atherosclerosis Risk. https://app.cochat.ai/papers/10.1371/journal.pgen.1001233
The paper
Burd, C. E., Jeck, W. R., Liu, Y., Sanoff, H. K., Wang, Z., & Sharpless, N. E. (2010). Expression of Linear and Novel Circular Forms of an INK4/ARF-Associated Non-Coding RNA Correlates with Atherosclerosis Risk. PLoS Genetics. https://doi.org/10.1371/journal.pgen.1001233

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.