Author/Authors :
Ghadiri, Hamed Faculty of Biological Sciences - Tarbiat Modares University, Tehran 14115-175, Iran , Alavi, Sana Faculty of Biological Sciences - Tarbiat Modares University, Tehran 14115-175, Iran , Dabirmanesh, Bahareh Faculty of Biological Sciences - Tarbiat Modares University, Tehran 14115-175, Iran , Moriyama, Kenji Department of Genome Medicine - Tokyo Metropolitan Institute of Medical Science, Setagaya-ku, Japan , Khajeh, Khosro Faculty of Biological Sciences - Tarbiat Modares University, Tehran 14115-175, Iran , Masai, Hisao Faculty of Biological Sciences - Tarbiat Modares University, Tehran 14115-175, Iran
Abstract :
DNA replication starts from a specific point on the
chromosome that is called the origin of replication. In
contrast to prokaryotes in which DNA replication starts
from a single origin, eukaryotic DNA replication starts
from many origins scattered along the chromosomes.
Budding yeast contains 300 origins, whereas fission yeast
has 1,100, and the numbers of replication origins for
human increase to over 20,000. These origins are fired in
a coordinated manner, and there are spatial and temporal
disciplines for this process, which happens in the S phase
of the cell cycle. It was known that eukaryotic cells
prepare all these potential origins during the G1 phase of
the cell cycle but utilize only a portion of these origins
during S phase. Furthermore, firing some of these origins
are delayed until the mid and late phases of the S phase.
Coordinated activation of these origins occurs under
“Replication Timing Program”. The segments of the
chromosome containing co-regulated origins that fire
simultaneously are named “Replication Timing
Domains”, ranging in size from 100 kb to 1 Mb.
Replication timing is determined at a specific time in the
early G1 phase that is called Timing Decision Point
(TDP). Studies have shown that major chromosome
repositioning occurs at TDP. Generally, replication timing
domains are classified into three classes including Early,
Mid and Late.