TY - JOUR
T1 - RNase-dependent discontinuities associated with the crossovers of spontaneously formed joint DNA molecules in Physarum polycephalum
AU - Maric, Chrystelle
AU - Bénard, Marianne
AU - Pierron, Gérard
N1 - Funding Information:
Acknowledgments We thank members of the GDR 2915 “Replication of eukaryotic chromosomes and its checkpoints” and especially Etienne Schwob for helpful advice and discussions. We thank Rodney Rothstein for constructive discussions of our data and also Kathrin Marheineke for critical reading of the manuscript. This work was supported by a general funding from the CNRS, grant L494 from Association de la Recherche Contre le Cancer, and by grant ORC454 from Ligue Nationale Contre le Cancer.
PY - 2010/12/1
Y1 - 2010/12/1
N2 - Transient four stranded joint DNA molecules bridging sister chromatids constitute an intriguing feature of replicating genomes. Here, we studied their structure and frequency of formation in Physarum polycephalum. By "3D gels", we evidenced that they are not made of four continuous DNA strands. Discontinuities, which do not interfere with the unique propensity of the joint DNA molecules to branch migrate in vitro, are linked to the crossover, enhanced by RNaseA, and affect at most half of the DNA strands. We propose a structural model of joint DNA molecules containing ribonucleotides inserted within one strand, a gapped strand, and two continuous DNA strands. We further show that spontaneous joint DNA molecules are short-lived and are as abundant as replication forks. Our results emphasize the highly frequent formation of joint DNA molecules involving newly replicated DNA in an untreated cell and uncover a transitory mechanism connecting the sister chromatids during S phase.
AB - Transient four stranded joint DNA molecules bridging sister chromatids constitute an intriguing feature of replicating genomes. Here, we studied their structure and frequency of formation in Physarum polycephalum. By "3D gels", we evidenced that they are not made of four continuous DNA strands. Discontinuities, which do not interfere with the unique propensity of the joint DNA molecules to branch migrate in vitro, are linked to the crossover, enhanced by RNaseA, and affect at most half of the DNA strands. We propose a structural model of joint DNA molecules containing ribonucleotides inserted within one strand, a gapped strand, and two continuous DNA strands. We further show that spontaneous joint DNA molecules are short-lived and are as abundant as replication forks. Our results emphasize the highly frequent formation of joint DNA molecules involving newly replicated DNA in an untreated cell and uncover a transitory mechanism connecting the sister chromatids during S phase.
UR - http://www.scopus.com/inward/record.url?scp=78649294825&partnerID=8YFLogxK
U2 - 10.1007/s00412-010-0281-x
DO - 10.1007/s00412-010-0281-x
M3 - Article
C2 - 20607271
AN - SCOPUS:78649294825
SN - 0009-5915
VL - 119
SP - 601
EP - 611
JO - Chromosoma
JF - Chromosoma
IS - 6
ER -