TY - JOUR
T1 - A replicase clamp-binding dynamin-like protein promotes colocalization of nascent DNA strands and equipartitioning of chromosomes in E.coli
AU - Ozaki, Shogo
AU - Matsuda, Yusaku
AU - Keyamura, Kenji
AU - Kawakami, Hironori
AU - Noguchi, Yasunori
AU - Kasho, Kazutoshi
AU - Nagata, Komomo
AU - Masuda, Tamami
AU - Sakiyama, Yukari
AU - Katayama, Tsutomu
N1 - Funding Information:
We thank Hironori Niki for helpful discussions, Jun-ichi Kato and NBRP-NIG for the E. coli strains, the Kyushu University Research Support Center for sequencing, and Urs Jenal for suggestions and support to S.O. in his laboratory during the revision of the manuscript. This study was supported by KAKENHI (no. 17080005, 22370064, and 25117516) from MEXT of Japan. K. Kasho received a predoctoral fellowship from JSPS.
PY - 2013/5/12
Y1 - 2013/5/12
N2 - In Escherichia coli, bidirectional chromosomal replication is accompanied by the colocalization of sister replication forks. However, the biological significance of this mechanism and the key factors involved are still largely unknown. In this study, we found that a protein, termed CrfC, helps sustain the colocalization of nascent DNA regions of sister replisomes and promote chromosome equipartitioning. CrfC formed homomultimers that bound to multiple molecules of the clamp, a replisome subunit that encircles DNA, and colocalized with nascent DNA regions in a clamp-binding-dependent manner in living cells. CrfC is a dynamin homolog; however, it lacks the typical membrane-binding moiety and instead possesses a clamp-binding motif. Given that clamps remain bound to DNA after Okazaki fragment synthesis, we suggest that CrfC sustains the colocalization of sister replication forks in a unique manner by linking together the clamp-loaded nascent DNA strands, thereby laying the basis for subsequent chromosome equipartitioning
AB - In Escherichia coli, bidirectional chromosomal replication is accompanied by the colocalization of sister replication forks. However, the biological significance of this mechanism and the key factors involved are still largely unknown. In this study, we found that a protein, termed CrfC, helps sustain the colocalization of nascent DNA regions of sister replisomes and promote chromosome equipartitioning. CrfC formed homomultimers that bound to multiple molecules of the clamp, a replisome subunit that encircles DNA, and colocalized with nascent DNA regions in a clamp-binding-dependent manner in living cells. CrfC is a dynamin homolog; however, it lacks the typical membrane-binding moiety and instead possesses a clamp-binding motif. Given that clamps remain bound to DNA after Okazaki fragment synthesis, we suggest that CrfC sustains the colocalization of sister replication forks in a unique manner by linking together the clamp-loaded nascent DNA strands, thereby laying the basis for subsequent chromosome equipartitioning
UR - http://www.scopus.com/inward/record.url?scp=84884129678&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84884129678&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2013.07.040
DO - 10.1016/j.celrep.2013.07.040
M3 - Article
C2 - 23994470
AN - SCOPUS:84884129678
SN - 2211-1247
VL - 4
SP - 985
EP - 995
JO - Cell Reports
JF - Cell Reports
IS - 5
ER -