Pre-mRNA splicing is an essential step of the expression of most metazoan protein-coding genes, which is often regulated in a cell type-specific or developmental manner. We have demonstrated previously that human DNA topoisomerase I, an extensively studied target for anticancer drugs, also has an intrinsic protein kinase activity that specifically phosphorylates proteins involved in splice site selection. Therefore, DNA topoisomerase I was recently shown to play a critical role in alternative splicing. Here, we have exploited these novel properties of DNA topoisomerase I to develop entirely novel diospyrin derivatives targeting its protein kinase activity and thereby modulating pre-mRNA splicing. Although some derivatives indeed inhibit kinase activity of topoisomerase I, they did not block reactions of topoisomerase I on DNA. However, these drugs interfere with camptothecin-dependent topoisomerase I-mediated DNA cleavage, implying that diospyrin derivatives mediate a conformational change of topoisomerase I. It is noteworthy that in vitro splicing reactions revealed that diospyrin derivatives alter various steps of splicing. Some diospyrin derivatives inhibit either the first or the second catalytic step of splicing but not spliceosome assembly, whereas diospyrin itself prevents the formation of full spliceosome. Our data revealed for the first time that diospyrin derivatives are able to stall the dynamic assembly of the spliceosome and open the exciting possibility of using these derivatives to correct aberrant splicing in human genetic diseases.
Selective inhibition of topoisomerase I and various steps of spliceosome assembly by diospyrin derivatives
Tazi, J.; Bakkour, N.; Soret, J.; Zekri, L.; Hazra, B.; Laine, W.; Baldeyrou, B.; Lansiaux, A.; Bailly, C.
2005-04 / vol 67 / pages 1186-1194
IGMM team(s) involved in this publication
spinal muscular-atrophy; antisense oligonucleotides; anticancer drugs; DNA-topoisomerase; kinase-activity; leishmania-donovani; small nuclear ribonucleoprotein; splicing factor; synthetic derivatives; terminal domain