scholarly journals Rif1 Binding and Control of Chromosome-Internal DNA Replication Origins Is Limited by Telomere Sequestration

Cell Reports ◽  
2018 ◽  
Vol 23 (4) ◽  
pp. 983-992 ◽  
Author(s):  
Lukas Hafner ◽  
Aleksandra Lezaja ◽  
Xu Zhang ◽  
Laure Lemmens ◽  
Maksym Shyian ◽  
...  
Keyword(s):  
Dna Replication ◽  
Replication Origins ◽  
Dna Replication Origins ◽  
And Control

scholarly journals Functional analysis of plastid DNA replication origins in tobacco by targeted inactivation

2002 ◽  
Vol 32 (2) ◽  
pp. 175-184 ◽  
Author(s):  
Stefan K. Mühlbauer ◽  
Andreas Lössl ◽  
Lilia Tzekova ◽  
Zhurong Zou ◽  
Keyword(s):  
Functional Analysis ◽  
Dna Replication ◽  
Plastid Dna ◽  
Replication Origins ◽  
Dna Replication Origins ◽  
Targeted Inactivation

scholarly journals Accelerated growth in the absence of DNA replication origins

Nature ◽  
2013 ◽  
Vol 503 (7477) ◽  
pp. 544-547 ◽  
Author(s):  
Michelle Hawkins ◽  
Sunir Malla ◽  
Martin J. Blythe ◽  
Conrad A. Nieduszynski ◽  
Thorsten Allers
Keyword(s):  
Dna Replication ◽  
Replication Origins ◽  
Accelerated Growth ◽  
Dna Replication Origins

Method of mapping DNA replication origins

1985 ◽  
Vol 5 (1) ◽  
pp. 85-92
Author(s):  
L D Spotila ◽  
J A Huberman
Keyword(s):  
Dna Replication ◽  
Simian Virus 40 ◽  
Simian Virus ◽  
Replication Forks ◽  
Replication Origins ◽  
Chromosomal Dna ◽  
Dna Restriction Fragments ◽  
Dna Restriction ◽  
Dna Replication Origins

We have developed a method which allows determination of the direction in which replication forks move through segments of chromosomal DNA for which cloned probes are available. The method is based on the facts that DNA restriction fragments containing replication forks migrate more slowly through agarose gels than do non-fork-containing fragments and that the extent of retardation of the fork-containing fragments is a function of the extent of replication. The procedure allows the identification of DNA replication origins as sites from which replication forks diverge. In this paper we demonstrate the feasibility of this procedure, with simian virus 40 DNA as a model, and we discuss its applicability to other systems.

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