Dictionary:
cy·to·ki·ne·sis (sī'tō-kə-nē'sĭs, -kī-) ![]() |
The division of the cytoplasm of a cell following the division of the nucleus.
cytokinetic cy'to·ki·net'ic (-nĕt'ĭk) adj.
Dictionary:
cy·to·ki·ne·sis (sī'tō-kə-nē'sĭs, -kī-) ![]() |
The division of the cytoplasm of a cell following the division of the nucleus.
cytokinetic cy'to·ki·net'ic (-nĕt'ĭk) adj.| 5min Related Video: cytokinesis |
| Sci-Tech Encyclopedia: Cytokinesis |
The physical partitioning of a plant or animal cell into two daughter cells during cell reproduction. There are two modes of cytokinesis: by a constriction (the cleavage furrow in animal cells and some plant cells) or from within by an expanding cell plate (the phragmoplast of many plant cells). In either mode, cytokinesis requires only a few minutes, beginning at variable times after the segregation of chromosomes during mitosis (nuclear division). In the vast majority of cases the resulting daughter cells are completely separated. Since they are necessarily smaller cells as a result of cytokinesis, most cells grow in volume between divisions.
Occasionally, cytokinesis is only partial, permitting nutrients and metabolites to be shared between cells. Should cytokinesis fail to occur at all, mitosis may cause more than one nucleus to accumulate. Such a cell is a syncytium. Some tissues normally contain syncytia, for example, binucleate cells in the liver and multinucleate plant endosperm. Some whole organisms such as slime molds are syncytial.
Cytokinesis is precisely and indispensably linked to mitosis, yet the timing and actual mechanisms are distinct. The plane of cell partitioning is perpendicular to the axis of mitosis and coincides with the plane previously occupied by the chromosomes at metaphase. Despite the reliability of this correlation, the chromosomes themselves are not essential for cytokinesis. Experiments performed upon living cells have shown that it is the cell's machinery for chromosome separation, the mitotic apparatus, that provides the essential positional signal to other parts of the cytoplasm which initiates cytokinesis. Subsequently, the mitotic apparatus is no longer involved in cytokinesis and can be destroyed or even sucked out without affecting cytokinesis. See also Chromosome; Mitosis.
A cleavage furrow develops by circumferential contraction of the peripheral cytoplasm, usually at the cell's equator. The mechanism of furrowing is very similar among a wide diversity of cell types in lower and higher animals and certain plants. The physical forces of contraction exhibited by a cleavage furrow are evidently greater than the forces of resistance elsewhere. Electron microscopic analysis of the peripheral cytoplasm beneath the cleavage furrow consistently reveals a specialization called the contractile ring. This transient cell organelle is composed of numerous long, thin protein fibers oriented circumferentially within the plane of furrowing. These microfilaments are about 5 nanometers in thickness, appear to attach to the cell membrane, and are known to be composed of actin intermixed with myosin. Both of these proteins are intimately involved in force generation in muscle cells. Thus, the present theory of cytokinesis by furrowing implicates the contractile ring as a transient, localized intracellular “muscle” that squeezes the cell in two. See also Muscle proteins.
In plant cells the dominant mode of cytokinesis involves a phragmoplast, a structure composed of fibrous and vesicular elements that resemble parts of the mitotic apparatus. Microtubules (the fibers) appear to convey a stream of small membranous vesicles toward the midline where they fuse into a pair of partitioning cell membranes. Cellulose cell walls are subsequently secreted between these membranes to solidify the separation between daughter cells. This mode of cytokinesis is well suited to plant cells whose stiff cell walls cannot participate in furrowing. Surprisingly, however, there are instances among the algae where cleavage furrows are the normal mode of cytokinesis. Occasionally, both cleavage furrows and phragmoplasts are employed in the same cell. See also Cell walls (plant); Plant cell.
| Veterinary Dictionary: cytokinesis |
The division of the cytoplasm between daughter cells in mitosis or meiosis.
| Wikipedia: Cytokinesis |
Cytokinesis is the process in which the cytoplasm of a single eukaryotic cell is divided to form two daughter cells. It usually initiates during the late stages of mitosis, and sometimes meiosis, splitting a binucleate cell in two, to ensure that chromosome number is maintained from one generation to the next. In animal cells, one notable exception to the normal process of cytokinesis is oogenesis (the creation of an ovum in the ovarian follicle of the ovary), where the ovum takes almost all the cytoplasm and organelles, leaving very little for the resulting polar bodies, which then die. In plant cells, a dividing structure known as the cell plate forms across the centre of the cytoplasm and a new cell wall forms between the two daughter cells.
Cytokinesis is distinguished from the prokaryotic process of binary fission.
Contents |
During different proliferative divisions, animal cell cytokinesis begins shortly after the onset of sister chromatid separation in the anaphase of mitosis. A contractile ring, made of non-muscle myosin II and actin filaments, assembles equatorially (in the middle of the cell) at the cell cortex (adjacent to the cell membrane). Myosin II uses the free energy released when ATP is hydrolysed to move along these actin filaments, constricting the cell membrane to form a cleavage furrow. Continued hydrolysis causes this cleavage furrow to ingress (move inwards), a striking process that is clearly visible down a light microscope. Ingression continues until a so-called midbody structure (composed of electron-dense, proteinaceous material) is formed and the process of abscission then physically cleaves this midbody into two. Abscission depends on septin filaments beneath the cleavage furrow, which provide a structural basis to ensure completion of cytokinesis. After cytokinesis, non-kinetochore microtubules reorganize and disappear into a new cytoskeleton as the cell cycle returns to interphase (see also cell cycle).
The position at which the contractile ring assembles is dictated by the mitotic spindle[1]. This seems to depend upon the GTPase RhoA, which influences several downstream effectors (such as the protein kinases ROCK and citron) to promote myosin activation (by influencing the phosphorylation of Myosin regulatory light chain (rMLC)) and actin filament assembly (by regulating formin protein) at a particular region of the cell cortex.[2]
Simultaneous with contractile ring assembly during prophase, a microtubule based structure termed the central spindle (or spindle midzone) forms when non-kinetochore microtubule fibres are bundled between the spindle poles. A number of different species including H. sapiens, D. melanogaster and C. elegans require the central spindle in order to efficiently undergo cytokinesis, although the specific phenotype described when it is absent varies from one species to the next (for example, certain Drosophila cell types are incapable of forming a cleavage furrow without the central spindle, whereas in both C. elegans embryos and human tissue culture cells a cleavage furrow is observed to form and ingress, but then regress before cytokinesis is complete). Seemingly vital for the formation of the central spindle (and therefore efficient cytokinesis) is a heterotetrameric protein complex called centralspindlin. Along with associated factors (such as SPD-1 in C. elegans), centralspindlin plays a role in bundling microtubules to form the spindle midzone during anaphase.
Cytokinesis must be temporally controlled to ensure that it occurs only after sister chromatid separation during normal proliferative cell divisions. To achieve this, many components of the cytokinesis machinery are highly regulated to ensure that they are able to perform a particular function at only a particular stage of the cell cycle.[3][4]
Due to the presence of a cell wall, cytokinesis in plant cells is significantly different from that in animal cells. Rather than forming a contractile ring, plant cells construct a cell plate in the middle of the cell. The Golgi apparatus releases vesicles containing cell wall materials. These vesicles fuse at the equatorial plane and form a cell plate. The cell plate begins as a fusion tube network, which then becomes a tubulo-vesicular network (TVN) as more components are added. The TVN develops into a tubular network, which then becomes a fenestrated sheet which adheres to the existing plasma membrane.
In bacterial cells, a tubulin-like protein called FtsZ was observed to be distributed equally in the cell, but seen to be forming a ring when cytokinesis takes place. The FtsZ ring becomes narrower by GTP hydrolysis. FtsZ recruits other Fts proteins to the site, among other mureine transpeptidases. It is strongly suggested that the polar regions of a bacterium exclude FtsZ, thereby assuring that the contractile ring forms in the middle of the cell.[5]
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| -kinesis | |
| cell cycle (cell and molecular biology) | |
| cell plate (cell and molecular biology) |
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![]() | Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2007. Published by Houghton Mifflin Company. All rights reserved. Read more | |
![]() | Sci-Tech Encyclopedia. McGraw-Hill Encyclopedia of Science and Technology. Copyright © 2005 by The McGraw-Hill Companies, Inc. All rights reserved. Read more | |
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![]() | Wikipedia. This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Cytokinesis". Read more |
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