TY - JOUR
T1 - Site-specific initiation of DNA replication within the non-transcribed spacer of Physarum rDNA
AU - Bénard, Marianne
AU - Lagnel, Claire
AU - Pierron, Gérard
N1 - Funding Information:
We thank Richard Braun (Bern, Switzerland) for providing us with plasmids containing rDNA fragments, Olivier Hyrien (Paris, France) for hybridization quantitation on Phosphorlmager, Jacqueline P6dron for expert technical assistance and Dominick Pallotta (Quebec, Canada) for critical reading of the manuscript. This work was supported by general funding of the CNRS and by grant 1301 of Asssociation de la Recherche sur le Cancer, Villejuif.
PY - 1995/5/11
Y1 - 1995/5/11
N2 - Physarum polycephalum rRNA genes are found on extrachromosomal 60 kb linear palindromlc DNA molecules. Previous work using electron microscope visualization suggested that these molecules are duplicated from one of four potential replication origins located in the 24 kb central non-transcribed spacer [Vogt and Braun (1977) Eur. J. Blochem., 80, 557-566]. Considering the controversy on the nature of the replication origins in eukaryotic cells, where both site-specific or delocallzed Initiations have been described, we study here Physarum rDNA replication by two dimensional agarose gel electrophoresls and compare the results to those obtained by electron microscopy. Without the need of cell treatment or enrichment in replication Intermediates, we detect hybridization signals corresponding to replicating rDNA fragments throughout the cell cycle, confirming that the synthesis of rDNA molecules is not under the control of S-phase. The patterns of replication intermediates along rDNA minichromosomes are consistent with the existence of four site-specific replication origins, whose localization in the central non-transcribed spacer is in agreement with the electron microscope mapping. It Is also shown that, on a few molecules, at least two origins are active simultaneously.
AB - Physarum polycephalum rRNA genes are found on extrachromosomal 60 kb linear palindromlc DNA molecules. Previous work using electron microscope visualization suggested that these molecules are duplicated from one of four potential replication origins located in the 24 kb central non-transcribed spacer [Vogt and Braun (1977) Eur. J. Blochem., 80, 557-566]. Considering the controversy on the nature of the replication origins in eukaryotic cells, where both site-specific or delocallzed Initiations have been described, we study here Physarum rDNA replication by two dimensional agarose gel electrophoresls and compare the results to those obtained by electron microscopy. Without the need of cell treatment or enrichment in replication Intermediates, we detect hybridization signals corresponding to replicating rDNA fragments throughout the cell cycle, confirming that the synthesis of rDNA molecules is not under the control of S-phase. The patterns of replication intermediates along rDNA minichromosomes are consistent with the existence of four site-specific replication origins, whose localization in the central non-transcribed spacer is in agreement with the electron microscope mapping. It Is also shown that, on a few molecules, at least two origins are active simultaneously.
UR - http://www.scopus.com/inward/record.url?scp=0029070940&partnerID=8YFLogxK
U2 - 10.1093/nar/23.9.1447
DO - 10.1093/nar/23.9.1447
M3 - Article
C2 - 7784195
AN - SCOPUS:0029070940
SN - 0305-1048
VL - 23
SP - 1447
EP - 1453
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 9
ER -