{"id":772,"date":"2017-11-11T18:54:45","date_gmt":"2017-11-11T18:54:45","guid":{"rendered":"https:\/\/pressbooks.hcfl.edu\/bio1\/chapter\/the-eukaryotic-cell-cycle\/"},"modified":"2025-08-29T18:29:43","modified_gmt":"2025-08-29T18:29:43","slug":"the-eukaryotic-cell-cycle","status":"publish","type":"chapter","link":"https:\/\/pressbooks.hcfl.edu\/bio1\/chapter\/the-eukaryotic-cell-cycle\/","title":{"raw":"The Eukaryotic Cell Cycle","rendered":"The Eukaryotic Cell Cycle"},"content":{"raw":"Eukaryotes have two major types of cell division: mitosis and meiosis. Mitosis is used to produce new body cells for growth and healing, while meiosis is used to produce sex cells (eggs and sperm). Meiosis will be discussed in a later chapter.\n\nThe cell cycle <\/strong>is an ordered series of events involving cell growth and cell division that produces two new daughter cells via mitosis. The length of the cell cycle is highly variable even within the cells of an individual organism. In humans, the frequency of cell turnover ranges from a few hours in early embryonic development to an average of two to five days for epithelial cells, or to an entire human lifetime spent without dividing in specialized cells such as cortical neurons or cardiac muscle cells. There is also variation in the time that a cell spends in each phase of the cell cycle. When fast-dividing mammalian cells are grown in culture (outside the body under optimal growing conditions), the length of the cycle is approximately 24 hours. The timing of events in the cell cycle is controlled by mechanisms that are both internal and external to the cell.\n\nCells on the path to cell division proceed through a series of precisely timed and carefully regulated stages of growth, DNA replication, and division that produce two genetically identical cells. The cell cycle has two major phases: interphase and the mitotic phase (Figure 1<\/strong>). During interphase<\/strong>, the cell grows and DNA is replicated. During the mitotic phase<\/strong>, the replicated DNA and cytoplasmic contents are separated and the cell divides.\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"Cell Figure 1:<\/strong> A cell moves through a series of phases in an orderly manner. During interphase, G1 involves cell growth and protein synthesis, the S phase involves DNA replication and the replication of the centrosome, and G2 involves further growth and protein synthesis. The mitotic phase follows interphase. Mitosis is nuclear division during which duplicated chromosomes are segregated and distributed into daughter nuclei. Usually the cell will divide after mitosis in a process called cytokinesis in which the cytoplasm is divided and two daughter cells are formed.[\/caption]\n

Interphase<\/h1>\nDuring interphase, the cell undergoes normal processes while also preparing for cell division. For a cell to move from interphase to the mitotic phase, many internal and external conditions must be met.\u00a0The three stages of interphase are called G1<\/sub>, S, and G2<\/sub>.\n\n
\n

G1<\/sub> Phase (First Gap)<\/h2>\n

The first stage of interphase is called the G1<\/sub> phase (first gap) because, from a microscopic aspect, little change is visible. However, during the G1<\/sub> stage, the cell is quite active at the biochemical level. The cell is accumulating the building blocks of chromosomal DNA and the associated proteins as well as accumulating sufficient energy reserves to complete the task of replicating each chromosome in the nucleus.<\/p>\n\n<\/section>

\n

S Phase (Synthesis of DNA)<\/h2>\n

Throughout interphase, nuclear DNA remains in a semi-condensed chromatin configuration. In the S phase, DNA replication can proceed through the mechanisms that result in the formation of identical pairs of DNA molecules\u2014sister chromatids<\/strong>\u2014that are firmly attached to the centromeric region (Figure 2<\/strong>).<\/p>\n\n\n[caption id=\"attachment_761\" align=\"alignnone\" width=\"286\"]\"\" Figure 2<\/strong> DNA replication during S phase copies each linear chromosome. The chromosomes remain attached together at a region called the centromere. Photo credit: Lisa Bartee[\/caption]\n\nThe centrosome<\/strong> is also duplicated during the S phase. The two centrosomes will give rise to the mitotic spindle, the apparatus that orchestrates the movement of chromosomes during mitosis. At the center of each animal cell, the centrosomes of animal cells are associated with a pair of rod-like objects, the centrioles,<\/strong> which are at right angles to each other. Centrioles help organize cell division. Centrioles are not present in the centrosomes of other eukaryotic species, such as plants and most fungi.\n\n[caption id=\"attachment_761\" align=\"alignnone\" width=\"1024\"]\"\" Figure 3<\/strong> (a) Structure of the centrioles making up the centrosome. (b) Centrioles give rise to the mitotic spindle (grey threadlike structures). Photo credit: CNX OpenStax Microbiology<\/a>.[\/caption]\n\n<\/section>

\n

G2<\/sub> Phase (Second Gap)<\/h2>\n

In the G2<\/sub> phase, the cell replenishes its energy stores and synthesizes proteins necessary for chromosome manipulation. Some cell organelles are duplicated, and the cytoskeleton is dismantled to provide resources for the mitotic phase. There may be additional cell growth during G2<\/sub>. The final preparations for the mitotic phase must be completed before the cell is able to enter the first stage of mitosis.<\/p>\n\n<\/section>\n

The Mitotic Phase<\/h1>\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"mitosis\" Figure 4:<\/strong> Mitosis in onion root cells. The cells in this image are in various stages of mitosis. (Credit: Spike Walker. Wellcome Images<\/a> images@wellcome.ac.uk)[\/caption]\n\nTo make two daughter cells, the contents of the nucleus and the cytoplasm must be divided. The mitotic phase is a multistep process during which the duplicated chromosomes are aligned, separated, and moved to opposite poles of the cell, and then the cell is divided into two new identical daughter cells. The first portion of the mitotic phase, mitosis<\/strong>, is composed of five stages, which accomplish nuclear division (Figure 5<\/strong>). The second portion of the mitotic phase, called cytokinesis,<\/strong> is the physical separation of the cytoplasmic components into two daughter cells. Although the stages of mitosis are similar for most eukaryotes, the process of cytokinesis is quite different for eukaryotes that have cell walls, such as plant cells.\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"1600\"]\"\" Figure 5<\/strong> Summary of the process of mitosis. Photo credit Oganesson007<\/a>, Wikimedia.[\/caption]\n

Prophase<\/h2>\n

During prophase, the \u201cfirst phase,\u201d the nuclear envelope starts to dissociate into small vesicles, and the membranous organelles (such as the Golgi apparatus and endoplasmic reticulum), fragment and disperse toward the edges of the cell. The nucleolus disappears. The centrosomes begin to move to opposite poles of the cell. Microtubules that will form the mitotic spindle extend between the centrosomes, pushing them farther apart as the microtubule fibers lengthen. The sister chromatids begin to coil more tightly with the aid of condensin proteins and become visible under a light microscope.<\/p>\n\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"\" Figure 6<\/strong>\u00a0Prophase. Photo credit Kelvin13<\/a>; Wikimedia.[\/caption]\n

Prometaphase<\/h2>\nDuring prometaphase,<\/strong> the \u201cfirst change phase,\u201d many processes that were begun in prophase continue to advance. The remnants of the nuclear envelope fragment. The mitotic spindle continues to develop as more microtubules assemble and stretch across the length of the former nuclear area. Chromosomes become more condensed and discrete. Each sister chromatid develops a protein structure called a kinetochore<\/strong> in the centromeric region.\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"\" Figure 7<\/strong>\u00a0Prometaphase. Photo credit Kelvin13<\/a>; Wikimedia.[\/caption]\n\nThe proteins of the kinetochore attract and bind mitotic spindle microtubules. As the spindle microtubules extend from the centrosomes, some of these microtubules come into contact with and firmly bind to the kinetochores. Once a mitotic fiber attaches to a chromosome, the chromosome will be oriented until the kinetochores of sister chromatids face the opposite poles. Eventually, all the sister chromatids will be attached via their kinetochores to microtubules from opposing poles. Spindle microtubules that do not engage the chromosomes are called polar microtubules. These microtubules overlap each other midway between the two poles and contribute to cell elongation. Astral microtubules are located near the poles, aid in spindle orientation, and are required for the regulation of mitosis.\n\n[caption id=\"attachment_771\" align=\"aligncenter\" width=\"540\"]\"This Figure 8<\/strong>\u00a0During prometaphase, mitotic spindle microtubules from opposite poles attach to each sister chromatid at the kinetochore. In anaphase, the connection between the sister chromatids breaks down, and the microtubules pull the chromosomes toward opposite poles.[\/caption]\n
<\/figure>\n

Metaphase<\/h2>\n

During metaphase,<\/strong> the \u201cchange phase,\u201d all the chromosomes are aligned in a plane called the metaphase plate, or the equatorial plane, midway between the two poles of the cell. The sister chromatids are still tightly attached to each other by cohesin proteins. At this time, the chromosomes are maximally condensed.<\/p>\n\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"\" Figure 9<\/strong>\u00a0Metaphase. Photo credit Kelvin13<\/a>; Wikimedia.[\/caption]\n

Anaphase<\/h2>\n

During anaphase, the \u201cupward phase,\u201d the cohesin proteins degrade, and the sister chromatids separate at the centromere. Each chromatid, now called a chromosome, is pulled rapidly toward the centrosome to which its microtubule is attached. The cell becomes visibly elongated (oval shaped) as the polar microtubules slide against each other at the metaphase plate where they overlap.<\/p>\n\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"\" Figure 10<\/strong>\u00a0Anaphase. Photo credit Kelvin13<\/a>; Wikimedia.[\/caption]\n

Telophase<\/h2>\n

During telophase, the \u201cdistance phase,\u201d the chromosomes reach the opposite poles and begin to decondense (unravel), relaxing into a chromatin configuration. The mitotic spindles are depolymerized into tubulin monomers that will be used to assemble cytoskeletal components for each daughter cell. Nuclear envelopes form around the chromosomes, and nucleosomes appear within the nuclear area.<\/p>\n\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"\" Figure 11<\/strong>\u00a0Telophase. Photo credit Kelvin13<\/a>; Wikimedia.[\/caption]\n

Cytokinesis<\/h1>\n

Cytokinesis,<\/strong> or \u201ccell motion,\u201d is the second main stage of the mitotic phase during which cell division is completed via the physical separation of the cytoplasmic components into two daughter cells. Division is not complete until the cell components have been divided and completely separated into the two daughter cells. Although the stages of mitosis are similar for most eukaryotes, the process of cytokinesis is quite different for eukaryotes that have cell walls, such as plant cells.<\/p>\n

In cells such as animal cells that lack cell walls, cytokinesis follows the onset of anaphase. A contractile ring composed of actin filaments forms just inside the plasma membrane at the former metaphase plate (Figure 12<\/strong>). The actin filaments pull the equator of the cell inward, forming a fissure. This fissure, or \u201ccrack,\u201d is called the cleavage furrow. The furrow deepens as the actin ring contracts, and eventually the membrane is cleaved in two.<\/p>\n

In plant cells, a new cell wall must form between the daughter cells. During interphase, the Golgi apparatus accumulates enzymes, structural proteins, and glucose molecules prior to breaking into vesicles and dispersing throughout the dividing cell (Figure 12<\/strong>). During telophase, these Golgi vesicles are transported on microtubules to form a phragmoplast (a vesicular structure) at the metaphase plate. There, the vesicles fuse and coalesce from the center toward the cell walls; this structure is called a cell plate. As more vesicles fuse, the cell plate enlarges until it merges with the cell walls at the periphery of the cell. Enzymes use the glucose that has accumulated between the membrane layers to build a new cell wall. The Golgi membranes become parts of the plasma membrane on either side of the new cell wall.<\/p>\n\n\n[caption id=\"attachment_771\" align=\"alignnone\" width=\"300\"]\"\" Figure 12<\/strong>\u00a0During cytokinesis in animal cells, a ring of actin filaments forms at the metaphase plate. The ring contracts, forming a cleavage furrow, which divides the cell in two. In plant cells, Golgi vesicles coalesce at the former metaphase plate, forming a phragmoplast. A cell plate formed by the fusion of the vesicles of the phragmoplast grows from the center toward the cell walls, and the membranes of the vesicles fuse to form a plasma membrane that divides the cell in two.[\/caption]\n

Summary of Mitosis and Cytokinesis<\/h1>\n\"\"\n\nFigure 13<\/strong>\u00a0Mitosis is divided into five stages\u2014prophase, prometaphase, metaphase, anaphase, and telophase. The pictures at the bottom were taken by fluorescence microscopy of cells artificially stained by fluorescent dyes: blue fluorescence indicates DNA (chromosomes) and green fluorescence indicates microtubules (spindle apparatus). (credit \u201cmitosis drawings\u201d: modification of work by Mariana Ruiz Villareal; credit \u201cmicrographs\u201d: modification of work by Roy van Heesbeen; credit \u201ccytokinesis micrograph\u201d: Wadsworth Center\/New York State Department of Health; scale-bar data from Matt Russell)\n

G0 Phase<\/h1>\nNot all cells adhere to the classic cell-cycle pattern in which a newly formed daughter cell immediately enters interphase, closely followed by the mitotic phase. Cells in the G<\/strong>0 phase <\/strong>are not actively preparing to divide. The cell is in a quiescent (inactive) stage, having exited the cell cycle. Some cells enter G0 temporarily until an external signal triggers the onset of G1. Other cells that never or rarely divide, such as mature cardiac muscle and nerve cells, remain in G0 permanently).\n

References<\/h1>\nUnless otherwise noted, images on this page are licensed under CC-BY 4.0 by OpenStax.\n\nOpenStax, Biology. OpenStax CNX. May 27, 2016 http:\/\/cnx.org\/contents\/s8Hh0oOc@9.10:Vbi92lHB@9\/The-Cell-Cycle","rendered":"

Eukaryotes have two major types of cell division: mitosis and meiosis. Mitosis is used to produce new body cells for growth and healing, while meiosis is used to produce sex cells (eggs and sperm). Meiosis will be discussed in a later chapter.<\/p>\n

The cell cycle <\/strong>is an ordered series of events involving cell growth and cell division that produces two new daughter cells via mitosis. The length of the cell cycle is highly variable even within the cells of an individual organism. In humans, the frequency of cell turnover ranges from a few hours in early embryonic development to an average of two to five days for epithelial cells, or to an entire human lifetime spent without dividing in specialized cells such as cortical neurons or cardiac muscle cells. There is also variation in the time that a cell spends in each phase of the cell cycle. When fast-dividing mammalian cells are grown in culture (outside the body under optimal growing conditions), the length of the cycle is approximately 24 hours. The timing of events in the cell cycle is controlled by mechanisms that are both internal and external to the cell.<\/p>\n

Cells on the path to cell division proceed through a series of precisely timed and carefully regulated stages of growth, DNA replication, and division that produce two genetically identical cells. The cell cycle has two major phases: interphase and the mitotic phase (Figure 1<\/strong>). During interphase<\/strong>, the cell grows and DNA is replicated. During the mitotic phase<\/strong>, the replicated DNA and cytoplasmic contents are separated and the cell divides.<\/p>\n

\"Cell
Figure 1:<\/strong> A cell moves through a series of phases in an orderly manner. During interphase, G1 involves cell growth and protein synthesis, the S phase involves DNA replication and the replication of the centrosome, and G2 involves further growth and protein synthesis. The mitotic phase follows interphase. Mitosis is nuclear division during which duplicated chromosomes are segregated and distributed into daughter nuclei. Usually the cell will divide after mitosis in a process called cytokinesis in which the cytoplasm is divided and two daughter cells are formed.<\/figcaption><\/figure>\n

Interphase<\/h1>\n

During interphase, the cell undergoes normal processes while also preparing for cell division. For a cell to move from interphase to the mitotic phase, many internal and external conditions must be met.\u00a0The three stages of interphase are called G1<\/sub>, S, and G2<\/sub>.<\/p>\n

\n

G1<\/sub> Phase (First Gap)<\/h2>\n

The first stage of interphase is called the G1<\/sub> phase (first gap) because, from a microscopic aspect, little change is visible. However, during the G1<\/sub> stage, the cell is quite active at the biochemical level. The cell is accumulating the building blocks of chromosomal DNA and the associated proteins as well as accumulating sufficient energy reserves to complete the task of replicating each chromosome in the nucleus.<\/p>\n<\/section>\n

\n

S Phase (Synthesis of DNA)<\/h2>\n

Throughout interphase, nuclear DNA remains in a semi-condensed chromatin configuration. In the S phase, DNA replication can proceed through the mechanisms that result in the formation of identical pairs of DNA molecules\u2014sister chromatids<\/strong>\u2014that are firmly attached to the centromeric region (Figure 2<\/strong>).<\/p>\n

\"\"
Figure 2<\/strong> DNA replication during S phase copies each linear chromosome. The chromosomes remain attached together at a region called the centromere. Photo credit: Lisa Bartee<\/figcaption><\/figure>\n

The centrosome<\/strong> is also duplicated during the S phase. The two centrosomes will give rise to the mitotic spindle, the apparatus that orchestrates the movement of chromosomes during mitosis. At the center of each animal cell, the centrosomes of animal cells are associated with a pair of rod-like objects, the centrioles,<\/strong> which are at right angles to each other. Centrioles help organize cell division. Centrioles are not present in the centrosomes of other eukaryotic species, such as plants and most fungi.<\/p>\n

\"\"
Figure 3<\/strong> (a) Structure of the centrioles making up the centrosome. (b) Centrioles give rise to the mitotic spindle (grey threadlike structures). Photo credit: CNX OpenStax Microbiology<\/a>.<\/figcaption><\/figure>\n<\/section>\n
\n

G2<\/sub> Phase (Second Gap)<\/h2>\n

In the G2<\/sub> phase, the cell replenishes its energy stores and synthesizes proteins necessary for chromosome manipulation. Some cell organelles are duplicated, and the cytoskeleton is dismantled to provide resources for the mitotic phase. There may be additional cell growth during G2<\/sub>. The final preparations for the mitotic phase must be completed before the cell is able to enter the first stage of mitosis.<\/p>\n<\/section>\n

The Mitotic Phase<\/h1>\n
\"mitosis\"
Figure 4:<\/strong> Mitosis in onion root cells. The cells in this image are in various stages of mitosis. (Credit: Spike Walker. Wellcome Images<\/a> images@wellcome.ac.uk)<\/figcaption><\/figure>\n

To make two daughter cells, the contents of the nucleus and the cytoplasm must be divided. The mitotic phase is a multistep process during which the duplicated chromosomes are aligned, separated, and moved to opposite poles of the cell, and then the cell is divided into two new identical daughter cells. The first portion of the mitotic phase, mitosis<\/strong>, is composed of five stages, which accomplish nuclear division (Figure 5<\/strong>). The second portion of the mitotic phase, called cytokinesis,<\/strong> is the physical separation of the cytoplasmic components into two daughter cells. Although the stages of mitosis are similar for most eukaryotes, the process of cytokinesis is quite different for eukaryotes that have cell walls, such as plant cells.<\/p>\n

\"\"
Figure 5<\/strong> Summary of the process of mitosis. Photo credit Oganesson007<\/a>, Wikimedia.<\/figcaption><\/figure>\n

Prophase<\/h2>\n

During prophase, the \u201cfirst phase,\u201d the nuclear envelope starts to dissociate into small vesicles, and the membranous organelles (such as the Golgi apparatus and endoplasmic reticulum), fragment and disperse toward the edges of the cell. The nucleolus disappears. The centrosomes begin to move to opposite poles of the cell. Microtubules that will form the mitotic spindle extend between the centrosomes, pushing them farther apart as the microtubule fibers lengthen. The sister chromatids begin to coil more tightly with the aid of condensin proteins and become visible under a light microscope.<\/p>\n

\"\"
Figure 6<\/strong>\u00a0Prophase. Photo credit Kelvin13<\/a>; Wikimedia.<\/figcaption><\/figure>\n

Prometaphase<\/h2>\n

During prometaphase,<\/strong> the \u201cfirst change phase,\u201d many processes that were begun in prophase continue to advance. The remnants of the nuclear envelope fragment. The mitotic spindle continues to develop as more microtubules assemble and stretch across the length of the former nuclear area. Chromosomes become more condensed and discrete. Each sister chromatid develops a protein structure called a kinetochore<\/strong> in the centromeric region.<\/p>\n

\"\"
Figure 7<\/strong>\u00a0Prometaphase. Photo credit Kelvin13<\/a>; Wikimedia.<\/figcaption><\/figure>\n

The proteins of the kinetochore attract and bind mitotic spindle microtubules. As the spindle microtubules extend from the centrosomes, some of these microtubules come into contact with and firmly bind to the kinetochores. Once a mitotic fiber attaches to a chromosome, the chromosome will be oriented until the kinetochores of sister chromatids face the opposite poles. Eventually, all the sister chromatids will be attached via their kinetochores to microtubules from opposing poles. Spindle microtubules that do not engage the chromosomes are called polar microtubules. These microtubules overlap each other midway between the two poles and contribute to cell elongation. Astral microtubules are located near the poles, aid in spindle orientation, and are required for the regulation of mitosis.<\/p>\n

\"This
Figure 8<\/strong>\u00a0During prometaphase, mitotic spindle microtubules from opposite poles attach to each sister chromatid at the kinetochore. In anaphase, the connection between the sister chromatids breaks down, and the microtubules pull the chromosomes toward opposite poles.<\/figcaption><\/figure>\n
<\/figure>\n

Metaphase<\/h2>\n

During metaphase,<\/strong> the \u201cchange phase,\u201d all the chromosomes are aligned in a plane called the metaphase plate, or the equatorial plane, midway between the two poles of the cell. The sister chromatids are still tightly attached to each other by cohesin proteins. At this time, the chromosomes are maximally condensed.<\/p>\n

\"\"
Figure 9<\/strong>\u00a0Metaphase. Photo credit Kelvin13<\/a>; Wikimedia.<\/figcaption><\/figure>\n

Anaphase<\/h2>\n

During anaphase, the \u201cupward phase,\u201d the cohesin proteins degrade, and the sister chromatids separate at the centromere. Each chromatid, now called a chromosome, is pulled rapidly toward the centrosome to which its microtubule is attached. The cell becomes visibly elongated (oval shaped) as the polar microtubules slide against each other at the metaphase plate where they overlap.<\/p>\n

\"\"
Figure 10<\/strong>\u00a0Anaphase. Photo credit Kelvin13<\/a>; Wikimedia.<\/figcaption><\/figure>\n

Telophase<\/h2>\n

During telophase, the \u201cdistance phase,\u201d the chromosomes reach the opposite poles and begin to decondense (unravel), relaxing into a chromatin configuration. The mitotic spindles are depolymerized into tubulin monomers that will be used to assemble cytoskeletal components for each daughter cell. Nuclear envelopes form around the chromosomes, and nucleosomes appear within the nuclear area.<\/p>\n

\"\"
Figure 11<\/strong>\u00a0Telophase. Photo credit Kelvin13<\/a>; Wikimedia.<\/figcaption><\/figure>\n

Cytokinesis<\/h1>\n

Cytokinesis,<\/strong> or \u201ccell motion,\u201d is the second main stage of the mitotic phase during which cell division is completed via the physical separation of the cytoplasmic components into two daughter cells. Division is not complete until the cell components have been divided and completely separated into the two daughter cells. Although the stages of mitosis are similar for most eukaryotes, the process of cytokinesis is quite different for eukaryotes that have cell walls, such as plant cells.<\/p>\n

In cells such as animal cells that lack cell walls, cytokinesis follows the onset of anaphase. A contractile ring composed of actin filaments forms just inside the plasma membrane at the former metaphase plate (Figure 12<\/strong>). The actin filaments pull the equator of the cell inward, forming a fissure. This fissure, or \u201ccrack,\u201d is called the cleavage furrow. The furrow deepens as the actin ring contracts, and eventually the membrane is cleaved in two.<\/p>\n

In plant cells, a new cell wall must form between the daughter cells. During interphase, the Golgi apparatus accumulates enzymes, structural proteins, and glucose molecules prior to breaking into vesicles and dispersing throughout the dividing cell (Figure 12<\/strong>). During telophase, these Golgi vesicles are transported on microtubules to form a phragmoplast (a vesicular structure) at the metaphase plate. There, the vesicles fuse and coalesce from the center toward the cell walls; this structure is called a cell plate. As more vesicles fuse, the cell plate enlarges until it merges with the cell walls at the periphery of the cell. Enzymes use the glucose that has accumulated between the membrane layers to build a new cell wall. The Golgi membranes become parts of the plasma membrane on either side of the new cell wall.<\/p>\n

\"\"
Figure 12<\/strong>\u00a0During cytokinesis in animal cells, a ring of actin filaments forms at the metaphase plate. The ring contracts, forming a cleavage furrow, which divides the cell in two. In plant cells, Golgi vesicles coalesce at the former metaphase plate, forming a phragmoplast. A cell plate formed by the fusion of the vesicles of the phragmoplast grows from the center toward the cell walls, and the membranes of the vesicles fuse to form a plasma membrane that divides the cell in two.<\/figcaption><\/figure>\n

Summary of Mitosis and Cytokinesis<\/h1>\n

\"\"<\/p>\n

Figure 13<\/strong>\u00a0Mitosis is divided into five stages\u2014prophase, prometaphase, metaphase, anaphase, and telophase. The pictures at the bottom were taken by fluorescence microscopy of cells artificially stained by fluorescent dyes: blue fluorescence indicates DNA (chromosomes) and green fluorescence indicates microtubules (spindle apparatus). (credit \u201cmitosis drawings\u201d: modification of work by Mariana Ruiz Villareal; credit \u201cmicrographs\u201d: modification of work by Roy van Heesbeen; credit \u201ccytokinesis micrograph\u201d: Wadsworth Center\/New York State Department of Health; scale-bar data from Matt Russell)<\/p>\n

G0 Phase<\/h1>\n

Not all cells adhere to the classic cell-cycle pattern in which a newly formed daughter cell immediately enters interphase, closely followed by the mitotic phase. Cells in the G<\/strong>0 phase <\/strong>are not actively preparing to divide. The cell is in a quiescent (inactive) stage, having exited the cell cycle. Some cells enter G0 temporarily until an external signal triggers the onset of G1. Other cells that never or rarely divide, such as mature cardiac muscle and nerve cells, remain in G0 permanently).<\/p>\n

References<\/h1>\n

Unless otherwise noted, images on this page are licensed under CC-BY 4.0 by OpenStax.<\/p>\n

OpenStax, Biology. OpenStax CNX. May 27, 2016 http:\/\/cnx.org\/contents\/s8Hh0oOc@9.10:Vbi92lHB@9\/The-Cell-Cycle<\/p>\n","protected":false},"author":130,"menu_order":3,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":["lisa-bartee-09rjouu9wq","shriner-waiter-xmtcidqjfm","catherine-creech-2ehqxneuz4"],"pb_section_license":"cc-by"},"chapter-type":[],"contributor":[91,89,90],"license":[53],"class_list":["post-772","chapter","type-chapter","status-publish","hentry","contributor-catherine-creech-2ehqxneuz4","contributor-lisa-bartee-09rjouu9wq","contributor-shriner-waiter-xmtcidqjfm","license-cc-by"],"part":753,"_links":{"self":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/772","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/users\/130"}],"version-history":[{"count":1,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/772\/revisions"}],"predecessor-version":[{"id":773,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/772\/revisions\/773"}],"part":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/parts\/753"}],"metadata":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/772\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/media?parent=772"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapter-type?post=772"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/contributor?post=772"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/license?post=772"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}