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The resulting structure has two branching "prongs", each one made up of a single strand of DNA. These two strands serve as the template for the leading and lagging strands, which will be created as DNA polymerase matches complementary nucleotides to the templates; the templates may be properly referred to as the leading strand template and the ...
A DNA polymerase is a member of a family of enzymes that catalyze the synthesis of DNA molecules from nucleoside triphosphates, the molecular precursors of DNA.These enzymes are essential for DNA replication and usually work in groups to create two identical DNA duplexes from a single original DNA duplex.
DNA gyrase is not the sole enzyme responsible for decatenation. In an experiment by Zechiedrich, Khodursky and Cozzarelli in 1997, it was found that topoisomerase IV is the only important decatenase of DNA replication intermediates in bacteria. [20] When DNA gyrase alone was inhibited, most of the catenanes were unlinked.
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.
DNA replication is a vital aspect of a cell's proliferation. Without replicating its DNA, a cell cannot divide and share its genetic information to progeny. In prokaryotes, like E. coli, DNA Pol III is the major polymerase involved with DNA replication. While DNA Pol II is not a major factor in chromosome replication, it has other roles to fill.
Required for initiation and elongation stages of DNA replication. Implicated in chromatin binding of Cdc45 and DNA polymerase α. Also required for stability of DNA polymerase α catalytic subunit in the budding yeast S. cerevisiae. Mrc1: Couple leading-strand synthesis with the CMG complex helicase activity. Metazoan homolog is known as Claspin.
Prokaryotic DNA Replication is the process by which a prokaryote duplicates its DNA into another copy that is passed on to daughter cells. [1] Although it is often studied in the model organism E. coli , other bacteria show many similarities. [ 2 ]
DnaA consists mainly in two different forms, the active ATP-form and the inactive ADP. [1] [3] The level of active DnaA within a cell is low immediately after a cell has divided. [1] Although the active form of DnaA requires ATP, the formation of the oriC/DnaA complex and subsequent DNA unwinding does not require ATP hydrolysis. [4]