Schematic representation for loss of chromosome cohesion and the Biology Diagrams Segregation of chromosomes in mitosis is preceded by chromosome reorganization into the characteristic mitotic shapes observed in most animal cells. This chromosome reorganization takes place during early mitosis (prophase and prometaphase) and involves two major structural changes. First, sister chromatids are resolved from each other while both sister chromatid cohesion and DNA catenation During mitosis and meiosis sister chromatids are held together by protein complexes. This cohesion is important not only for pairwise alignment of chromosomes on the mitotic spindle but also for the generation of tension across centromeres - it counteracts the pulling force of spindle microtubules, which ensures the bipolar attachment of chromosomes. Chromosome cohesion thus enables accurate In mitosis, cohesin maintains sister chromatid cohesion mainly at centromeres, while most cohesin is removed from chromosome arms until metaphase (meta). Condensins I and II are recruited to the chromatid axes and participate to construct mitotic chromosomes.
Abstract The faithful segregation of genetic information requires highly orchestrated changes of chromosome structure during the mitotic cell cycle. The linkage between duplicated sister DNAs is established during S phase and maintained throughout G2 phase (cohesion). In early mitosis, dramatic structural changes occur to produce metaphase chromosomes, each consisting of a pair of compacted
Chromosome Cohesion, Condensation, and Separation Biology Diagrams
Preparations for mitotic chromosome segregation begin in the S phase of the cell cycle, as each chromosome is copied to generate two identical sister chromatids and cohesion is established between
Cohesin is a ring-shaped protein complex that organises the genome, enabling its condensation, expression, repair and transmission. In this Primer, Makrantoni and Marston summarise the molecular functions and regulation of cohesin that underlie its central role in chromosome segregation during mitosis. While one of the primary roles for chromosome cohesion in bi-orientation and mitotic chromosome segregation is well-established, the complexities of the regulation of cohesion are still being discovered. Proper mitotic chromosome structure is essential for faithful chromosome segregation. Mounting evidence suggests that mitotic chromosome assembly is a progressive, dynamic process that requires topoisomerase II, condensins and cohesin and the activity of several signalling molecules. Current results suggest how these different activities might interact to achieve the familiar form of the
