Search results
Results from the WOW.Com Content Network
Eukaryotes initiate DNA replication at multiple points in the chromosome, so replication forks meet and terminate at many points in the chromosome. Because eukaryotes have linear chromosomes, DNA replication is unable to reach the very end of the chromosomes. Due to this problem, DNA is lost in each replication cycle from the end of the chromosome.
Required for initiation and elongation steps of DNA replication. A part of the Mcm2-7 helicase complex. Required after pre-RC step for loading of various proteins for initiation and elongation. Cdc45-Mcm-GINS (CMG) complex: Functional DNA helicase in eukaryotic cells Cdc6: Required for assembly of Mcm2-7 complex at ORC, in conjunction with Cdt1 .
The eukaryotic cell cycle consists of four distinct phases: G 1 phase, S phase (synthesis), G 2 phase (collectively known as interphase) and M phase (mitosis and cytokinesis). M phase is itself composed of two tightly coupled processes: mitosis, in which the cell's nucleus divides, and cytokinesis, in which the cell's cytoplasm and cell membrane divides forming two daughter cells.
Each D-loop contains an origin of replication for the heavy strand. Full circular DNA replication is initiated at that origin and replicates in only one direction. The middle strand in the D-loop can be removed and a new one will be synthesized that is not terminated until the heavy strand is fully replicated, or the middle strand can serve as a primer for the heavy strand replication.
Steps in DNA synthesis Throughout M phase and G1 phase, cells assemble inactive pre-replication complexes (pre-RC) on replication origins distributed throughout the genome. [ 4 ] During S-phase, the cell converts pre-RCs into active replication forks to initiate DNA replication. [ 4 ]
Studies in Xenopus revealed the Mcm2-7 complex is a critical component of DNA replication machinery. [6] Inactivation of temperature sensitive mutants of any of the Mcm proteins in "S. cerevisiae" caused DNA replication to halt if inactivation occurred during S phase, and prevented initiation of replication if inactivation occurred earlier. [6]
The DNA re-replication response is different from the response taken when damage is due to oxygen radical generation. Damage from oxygen radical generations leads to a response from the Myc oncogene, which phosphorylates p53 and H2AX. [16] The ATM/ATR DNA damage network will also respond to cases where there is an overexpression of Cdt1.
mismatch of bases, due to errors in DNA replication, in which the wrong DNA base is stitched into place in a newly forming DNA strand, or a DNA base is skipped over or mistakenly inserted. Monoadduct damage cause by change in single nitrogenous base of DNA; Di adduct damage; Damage caused by exogenous agents comes in many forms. Some examples are: