TY - JOUR
T1 - Chromosomal Translocation Formation Is Sufficient to Produce Fusion Circular RNAs Specific to Patient Tumor Cells
AU - Babin, Loelia
AU - Piganeau, Marion
AU - Renouf, Benjamin
AU - Lamribet, Khadija
AU - Thirant, Cecile
AU - Deriano, Ludovic
AU - Mercher, Thomas
AU - Giovannangeli, Carine
AU - Brunet, Erika C.
N1 - Publisher Copyright:
© 2018 The Authors
PY - 2018/7/27
Y1 - 2018/7/27
N2 - Circular RNAs constitute a unique class of RNAs whose precise functions remain to be elucidated. In particular, cancer-associated chromosomal translocations can give rise to fusion circular RNAs that play a role in leukemia progression. However, how and when fusion circular RNAs are formed and whether they are being selected in cancer cells remains unknown. Here, we used CRISPR/Cas9 to generate physiological translocation models of NPM1-ALK fusion gene. We showed that, in addition to generating fusion proteins and activating specific oncogenic pathways, chromosomal translocation induced by CRISPR/Cas9 led to the formation of de novo fusion circular RNAs. Specifically, we could recover different classes of circular RNAs composed of different circularization junctions, mainly back-spliced species. In addition, we identified fusion circular RNAs identical to those found in related patient tumor cells providing evidence that fusion circular RNAs arise early after chromosomal formation and are not just a consequence of the oncogenesis process.
AB - Circular RNAs constitute a unique class of RNAs whose precise functions remain to be elucidated. In particular, cancer-associated chromosomal translocations can give rise to fusion circular RNAs that play a role in leukemia progression. However, how and when fusion circular RNAs are formed and whether they are being selected in cancer cells remains unknown. Here, we used CRISPR/Cas9 to generate physiological translocation models of NPM1-ALK fusion gene. We showed that, in addition to generating fusion proteins and activating specific oncogenic pathways, chromosomal translocation induced by CRISPR/Cas9 led to the formation of de novo fusion circular RNAs. Specifically, we could recover different classes of circular RNAs composed of different circularization junctions, mainly back-spliced species. In addition, we identified fusion circular RNAs identical to those found in related patient tumor cells providing evidence that fusion circular RNAs arise early after chromosomal formation and are not just a consequence of the oncogenesis process.
KW - Cancer
KW - Molecular Biology
KW - Molecular Genetics
UR - http://www.scopus.com/inward/record.url?scp=85065848079&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2018.06.007
DO - 10.1016/j.isci.2018.06.007
M3 - Article
AN - SCOPUS:85065848079
SN - 2589-0042
VL - 5
SP - 19
EP - 29
JO - iScience
JF - iScience
ER -