Search results
Results from the WOW.Com Content Network
In late mitosis and early G1 phase, a large complex of initiator proteins assembles into the pre-replication complex at particular points in the DNA, known as "origins". [11] [10] In E. coli the primary initiator protein is Dna A; in yeast, this is the origin recognition complex. [27]
The initiator proteins are the proteins that recognize a specific DNA sequence within the origin of replication. The origin of replication is the site where the helicase attaches to the template strand and starts to unwind the DNA into two strands.
More than five decades ago, Jacob, Brenner, and Cuzin proposed the replicon hypothesis to explain the regulation of chromosomal DNA synthesis in E. coli. [18] The model postulates that a diffusible, trans-acting factor, a so-called initiator, interacts with a cis-acting DNA element, the replicator, to promote replication onset at a nearby origin.
The replication initiator protein (Rep) plays a key role in initiation of replication in plasmids. In its monomer form, Rep binds an iteron and promotes replication. The protein itself is known to contain two independent N-terminal and C-terminal globular domains that subsequently bind to two domains of the iteron.
The major enzymatic functions carried out at the replication fork are well conserved from prokaryotes to eukaryotes, but the replication machinery in eukaryotic DNA replication is a much larger complex, coordinating many proteins at the site of replication, forming the replisome.
This may not come as too much of a surprise, since the packaging of DNA with proteins and RNA into chromatin takes place immediately after the DNA is synthesized. Therefore, replication timing dictates the time of assembly of chromatin. Less intuitive is the relationship between replication timing and the three-dimensional positioning of ...
DnaA protein plays a crucial role in the initiation of chromosomal DNA replication. [3] Bound to ATP, and with the assistance of bacterial histone-like proteins [HU] DnaA then unwinds an AT-rich region near the left boundary of oriC, which carries three 13-mer motifs, [4] and opens up the double-stranded DNA for entrance of other replication ...
In E. coli, there are 11 GATC sites in the oriC that undergo hemimethylation during DNA replication. The protein SeqA binds to these sites preventing remethylation and blocking the binding of DnaA to low affinity sites for approximately one third of the cell cycle. However, SeqA does not block DnaA from binding to the R1, R2, and R4 sites.