No retraction, correction or concern found when last checked on Nov 1, 2026.
eccDNAs are apoptotic products with high innate immunostimulatory activity
Yuangao Wang, Meng Wang, Mohamed Nadhir Djekidel and 4 more
Nature · 2021
doi:10.1038/s41586-021-04009-w
Abstract
Extrachromosomal circular DNA elements (eccDNAs) have been described in the literature for several decades, and are known for their broad existence across different species1,2. However, their biogenesis and functions are largely unknown. By developing a new circular DNA enrichment method, here we purified and sequenced full-length eccDNAs with Nanopore sequencing. We found that eccDNAs map across the entire genome in a close to random manner, suggesting a biogenesis mechanism of random ligation of genomic DNA fragments. Consistent with this idea, we found that apoptosis inducers can increase eccDNA generation, which is dependent on apoptotic DNA fragmentation followed by ligation by DNA ligase 3. Importantly, we demonstrated that eccDNAs can function as potent innate immunostimulants in a manner that is independent of eccDNA sequence but dependent on eccDNA circularity and the cytosolic DNA sensor Sting. Collectively, our study not only revealed the origin, biogenesis and immunostimulant function of eccDNAs but also uncovered their sensing pathway and potential clinical implications in immune response. By developing a new eccDNA purification and profiling method, the study revealed close-to-random genomic origination, mechanism of biogenesis and function of eccDNAs.
Shown for reading. Its publisher allows quoting it, not republishing it.
References 53
- 1.
Paulsen T, Kumar P, Koseoglu MM & Dutta A. Discoveries of Extrachromosomal Circles of DNA in Normal and Tumor Cells. Trends Genet 34, 270–278, doi: (2018 ).
Not in our library10.1016/j.tig.2017.12.010
- 2.
Gaubatz JW. Extrachromosomal circular DNAs and genomic sequence plasticity in eukaryotic cells. Mutat Res 237, 271–292, doi: (1990 ).
Not in our library10.1016/0921-8734(90)90009-g
- 3.
Hotta Y. & Bassel A. Molecular Size and Circularity of DNA in Cells of Mammals and Higher Plants. Proc Natl Acad Sci U S A 53, 356–362, doi: (1965 ).
Not in our library10.1073/pnas.53.2.356
- 4.
- 5.
- 6.
Hull RM. Transcription-induced formation of extrachromosomal DNA during yeast ageing. PLoS Biol 17, e3000471, doi: (2019 ).
Not in our library10.1371/journal.pbio.3000471
- 7.
Gresham D. Adaptation to diverse nitrogen-limited environments by deletion or extrachromosomal element formation of the GAP1 locus. Proc Natl Acad Sci U S A 107, 18551–18556, doi: (2010 ).
Not in our library10.1073/pnas.1014023107
- 8.
Sinclair DA. & Guarente L. Extrachromosomal rDNA circles--a cause of aging in yeast. Cell 91, 1033–1042, doi: (1997 ).
Not in our library10.1016/s0092-8674(00)80493-6
- 9.
Shibata Y. Extrachromosomal microDNAs and chromosomal microdeletions in normal tissues. Science 336, 82–86, doi: (2012 ).
Not in our library10.1126/science.1213307
- 10.
Zhu J. Molecular characterization of cell-free eccDNAs in human plasma. Sci Rep 7, 10968, doi: (2017 ).
Not in our library10.1038/s41598-017-11368-w
- 11.
Cloninger C, Felton M, Paul B, Hirakawa Y. & Metzenberg S. Control of pH during plasmid preparation by alkaline lysis of Escherichia coli. Anal Biochem 378, 224–225, doi: (2008 ).
Not in our library10.1016/j.ab.2008.04.017
- 12.
DeLap RJ, Rush MG, Zouzias D. & Khan S. Isolation and preliminary characterization of the small circular DNA present in African green monkey kidney (BSC-1) cells. Plasmid 1, 508–521, doi: (1978 ).
Not in our library10.1016/0147-619x(78)90008-2
- 13.
- 14.
Tichy ED. Mechanisms maintaining genomic integrity in embryonic stem cells and induced pluripotent stem cells. Exp Biol Med (Maywood) 236, 987–996, doi: (2011 ).
Not in our library10.1258/ebm.2011.011107
- 15.
- 16.
Joffroy B, Uca YO, Presern D, Doye JPK. & Schmidt TL. Rolling circle amplification shows a sinusoidal template length-dependent amplification bias. Nucleic Acids Res 46, 538–545, doi: (2018 ).
Not in our library10.1093/nar/gkx1238
- 17.
Soh YQ. Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes. Cell 159, 800–813, doi: (2014 ).
Not in our library10.1016/j.cell.2014.09.052
- 18.
Sakahira H, Enari M. & Nagata S. Cleavage of CAD inhibitor in CAD activation and DNA degradation during apoptosis. Nature 391, 96–99, doi: (1998 ).
Not in our library10.1038/34214
- 19.
Li LY, Luo X. & Wang X. Endonuclease G is an apoptotic DNase when released from mitochondria. Nature 412, 95–99, doi: (2001 ).
Not in our library10.1038/35083620
- 20.
Shiokawa D, Kobayashi T. & Tanuma S. Involvement of DNase gamma in apoptosis associated with myogenic differentiation of C2C12 cells. J Biol Chem 277, 31031–31037, doi: (2002 ).
Not in our library10.1074/jbc.m204038200
- 21.
Arakawa H. Functional redundancy between DNA ligases I and III in DNA replication in vertebrate cells. Nucleic Acids Res 40, 2599–2610, doi: (2012 ).
Not in our library10.1093/nar/gkr1024
- 22.
Lu G. Ligase I and ligase III mediate the DNA double-strand break ligation in alternative end-joining. Proc Natl Acad Sci U S A 113, 1256–1260, doi: (2016 ).
Not in our library10.1073/pnas.1521597113
- 23.
Simsek D. Crucial role for DNA ligase III in mitochondria but not in Xrcc1-dependent repair. Nature 471, 245–248, doi: (2011 ).
Not in our library10.1038/nature09794
- 24.
Marichal T. DNA released from dying host cells mediates aluminum adjuvant activity. Nat Med 17, 996–1002, doi: (2011 ).
Not in our library10.1038/nm.2403
- 25.
Li Y, Berke IC. & Modis Y. DNA binding to proteolytically activated TLR9 is sequence-independent and enhanced by DNA curvature. EMBO J 31, 919–931, doi: (2012 ).
Not in our library10.1038/emboj.2011.441
- 26.
Lange SS. & Vasquez KM. HMGB1: the jack-of-all-trades protein is a master DNA repair mechanic. Mol Carcinog 48, 571–580, doi: (2009 ).
Not in our library10.1002/mc.20544
- 27.
Wang Z. Regulation of innate immune responses by DAI (DLM-1/ZBP1) and other DNA-sensing molecules. Proc Natl Acad Sci U S A 105, 5477–5482, doi: (2008 ).
Not in our library10.1073/pnas.0801295105
- 28.
Green DR, Ferguson T, Zitvogel L. & Kroemer G. Immunogenic and tolerogenic cell death. Nat Rev Immunol 9, 353–363, doi: (2009 ).
Not in our library10.1038/nri2545
- 29.
Sundaresan R, Parameshwaran HP, Yogesha SD, Keilbarth MW. & Rajan R. RNA-Independent DNA Cleavage Activities of Cas9 and Cas12a. Cell Rep 21, 3728–3739, doi: (2017 ).
Not in our library10.1016/j.celrep.2017.11.100
- 30.
Putney SD, Benkovic SJ. & Schimmel PR. A DNA fragment with an alpha-phosphorothioate nucleotide at one end is asymmetrically blocked from digestion by exonuclease III and can be replicated in vivo. Proc Natl Acad Sci U S A 78, 7350–7354, doi: (1981 ).
Not in our library10.1073/pnas.78.12.7350
- 31.
Sauer JD. The N-ethyl-N-nitrosourea-induced Goldenticket mouse mutant reveals an essential function of Sting in the in vivo interferon response to Listeria monocytogenes and cyclic dinucleotides. Infect Immun 79, 688–694, doi: (2011 ).
Not in our library10.1128/iai.00999-10
- 32.
Hou B, Reizis B. & DeFranco AL. Toll-like receptors activate innate and adaptive immunity by using dendritic cell-intrinsic and -extrinsic mechanisms. Immunity 29, 272–282, doi: (2008 ).
Not in our library10.1016/j.immuni.2008.05.016
- 33.
Oberhammer F. Apoptotic death in epithelial cells: cleavage of DNA to 300 and/or 50 kb fragments prior to or in the absence of internucleosomal fragmentation. EMBO J 12, 3679–3684 (1993 ).
Not in our library10.1002/j.1460-2075.1993.tb06042.x
- 34.
Shiokawa D. & Tanuma S. Differential DNases are selectively used in neuronal apoptosis depending on the differentiation state. Cell Death Differ 11, 1112–1120, doi: (2004 ).
Not in our library10.1038/sj.cdd.4401454
- 35.
Wang H. DNA ligase III as a candidate component of backup pathways of nonhomologous end joining. Cancer Res 65, 4020–4030, doi: (2005 ).
Not in our library10.1158/0008-5472.can-04-3055
- 36.
Cox D, Yuncken C. & Spriggs AI. Minute Chromatin Bodies in Malignant Tumours of Childhood. Lancet 1, 55–58, doi: (1965 ).
Not in our library10.1016/s0140-6736(65)90131-5
- 37.
Turner KM. Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity. Nature 543, 122–125, doi: (2017 ).
Not in our library10.1038/nature21356
- 38.
Li XD. Pivotal roles of cGAS-cGAMP signaling in antiviral defense and immune adjuvant effects. Science 341, 1390–1394, doi: (2013 ).
Not in our library10.1126/science.1244040
- 39.
Andreeva L. cGAS senses long and HMGB/TFAM-bound U-turn DNA by forming protein-DNA ladders. Nature 549, 394–398, doi: (2017 ).
Not in our library10.1038/nature23890
- 40.
Tovey MG, Lallemand C. & Thyphronitis G. Adjuvant activity of type I interferons. Biol Chem 389, 541–545, doi: (2008 ).
Not in our library10.1515/bc.2008.051
Cited by papers we hold 1
- Targeted profiling of human extrachromosomal DNA by CRISPR-CATCH · 2022No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.