Learning Objectives Associated with 2020_SS1_Bis2a_Facciotti_Reading_26
The cell cycle is an orderly sequence of events used by biological systems to coordinate cell division. In eukaryotes, asexual cell division proceeds via a cell cycle that includes multiple spatially and temporally coordinated events. These include a long preparatory period called interphase, and a mitotic phase called M phase. Interphase is often further divided into distinguishable subphases called G1, S, and G2 phases. Mitosis is
In asexually reproducing eukaryotic cells, one “turn” of the cell cycle
The first stage of interphase
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
Throughout interphase, nuclear DNA remains in a semi-condensed chromatin configuration. In S phase (synthesis phase), DNA replication results in the formation of two identical copies of each chromosome—sister chromatids—that
In cells using the organelles called centrosomes,
During the G2 phase, or second gap, the cell replenishes its energy stores and synthesizes the proteins necessary for chromosome manipulation. Some cell organelles
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 G0 phase 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.
A Quick Aside: Structure of Chromosomes During the Cell Cycle
If we lay out the DNA from all 46 chromosomes end to end, it would measure approximately two meters; however, its diameter would be only 2
Double-stranded DNA wraps around histone proteins to form nucleosomes that appear like “beads on a string.”
Mitosis and Cytokinesis
During the mitotic phase, a cell undergoes two major processes. First, it completes mitosis, during which the contents of the nucleus
The major phases of Mitosis are visually distinct from one another and
The stages of cell division oversee the separation of identical genetic material into two new nuclei, followed by the division of the cytoplasm.
Prophase is the first phase of mitosis, during which the loosely packed chromatin coils and condenses into visible chromosomes. During prophase, each chromosome becomes visible with its identical partner (sister chromatid) attached, forming the familiar X-shape of sister chromatids. The nucleolus disappears early during this phase, and the nuclear envelope also disintegrates.
A major occurrence during prophase concerns a very important structure that contains the origin site for microtubule growth. Cellular structures called centrioles that serve as origin points from which microtubules extend. These tiny structures also play a very important role during mitosis. A centrosome is a pair of centrioles together. The cell contains two centrosomes side-by-side, which
Near the end of prophase there is an invasion of the nuclear area by microtubules from the mitotic spindle. The nuclear membrane has disintegrated, and the microtubules attach themselves to the centromeres that adjoin pairs of sister chromatids. The kinetochore is a protein structure on the centromere that is the point of attachment between the mitotic spindle and the sister chromatids.
Metaphase is the second stage of mitosis. During this stage, the sister chromatids, with their attached microtubules, line up along a linear plane in the middle of the cell. A metaphase plate forms between the centrosomes that
Anaphase is the third stage of mitosis. Anaphase takes place over a few minutes, when the pairs of sister chromatids
Telophase is the final stage of mitosis.
Cytokinesis is the second part of the mitotic phase during which cell division
In cells such as animal cells that
In plant cells, a cleavage furrow is not possible because of the rigid cell walls surrounding the plasma membrane. 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 up into vesicles and dispersing throughout the dividing cell. During telophase, these Golgi vesicles move on microtubules to collect at the metaphase plate. There, the vesicles fuse from the center toward the cell walls; this structure
In part (a), a cleavage furrow forms at the former metaphase plate in the animal cell.
It is essential that daughter cells be nearly exact duplicates of the parent cell. Mistakes in the duplication or distribution of the chromosomes lead to mutations that may pass forward to every new cell produced from the abnormal cell. To prevent a compromised cell from continuing to divide, there are internal control mechanisms that operate at three main cell cycle checkpoints at which
The G1 checkpoint determines whether all conditions are favorable for cell division to proceed into S phase where DNA replication occurs. The G1 checkpoint, also called the restriction point, is the point at which the cell irreversibly commits to the cell-division process. Besides adequate reserves and cell size, there is a check for damage to the genomic DNA at the G1 checkpoint.
The G2 checkpoint bars
The M checkpoint occurs near the end of the metaphase stage of mitosis.
Watch what occurs at the G1, G2, and M checkpoints by visiting this animation of the cell cycle.
When the Cell Cycle gets out of Control
Most people understand that cancer or tumors
The process of a cell escaping its normal control system and becoming cancerous may
Homeostatic Imbalances: Cancer Arises from Homeostatic Imbalances
These two contrasting classes of genes, proto-oncogenes and tumor suppressor genes, are like the accelerator and brake pedal of the cell’s own “cruise control system,” respectively. Under normal conditions, these stop and go
A delicate homeostatic balance between the many proto-oncogenes and tumor suppressor genes delicately controls the cell cycle and ensures that only healthy cells replicate. Therefore, a disruption of this homeostatic balance can cause aberrant cell division and cancerous growths.
Sexual reproduction was an early evolutionary innovation after the appearance of eukaryotic cells. That most eukaryotes reproduce sexually is evidence of its evolutionary success. In many animals, it is the only mode of reproduction. And yet, scientists recognize some real disadvantages to sexual reproduction. On the surface, offspring that are genetically identical to the parent may appear to be more
However, multicellular organisms that
So why is sexual reproduction so common?
This is one of the important questions in biology and has been the focus of much research from the latter half of the twentieth century until now. A likely explanation is that the variation that sexual reproduction creates among offspring is very important to the survival and reproduction of those offspring. The only source of genetic variation in asexual organisms is mutation. In sexually reproducing organisms, mutations
The Red Queen Hypothesis
Each tiny advantage gained by favorable variation gives a species an edge over close competitors, predators, parasites, or even prey. The only method that will allow a
Sexual reproduction requires fertilization, the union of two cells from two individual organisms. If those two cells each contain one set of chromosomes, then the resulting cell contains two sets of chromosomes. Haploid cells contain one set of chromosomes, diploid cells contain two sets of chromosomes. The number of sets of chromosomes in a cell
The nuclear division that forms haploid cells, which
Early in prophase I, before the chromosomes can
As the nuclear envelope
Early in prophase I, homologous chromosomes come together to form a synapse.
The crossover events are the first source of genetic variation in the nuclei produced by meiosis. A single crossover event between homologous non-sister chromatids leads to a reciprocal exchange of equivalent DNA between a maternal chromosome and a paternal chromosome. Now, when that sister chromatid
Crossover occurs between non-sister chromatids of homologous chromosomes. The result is an exchange of genetic material between homologous chromosomes.
Possible NB Discussion Point
What are the major differences between Prophase I of Meiosis and Prophase of Mitosis? Why are these distinctions so significant?
The key event in prometaphase I
This randomness is the physical basis for the creation of the second form of genetic variation in offspring. Consider that the homologous chromosomes of a sexually reproducing organism
This event—the random (or independent) assortment of homologous chromosomes at the metaphase plate—is the second mechanism that introduces variation into the gametes or spores. In each cell that undergoes meiosis, the arrangement of the tetrads is different. The number of variations
To summarize the genetic consequences of meiosis I, the maternal and paternal genes
Random, independent assortment during
In anaphase I, the microtubules pull the linked chromosomes apart. The sister chromatids remain tightly bound
Telophase I and Cytokinesis
In telophase, the separated chromosomes arrive at opposite poles. The
Two haploid cells are the
In some species, cells enter a brief interphase, or interkinesis, before entering meiosis II. Interkinesis lacks an S phase, so
If the chromosomes
The nuclear envelopes
The sister chromatids are maximally condensed and aligned at the equator of the cell.
The sister chromatids
The process of chromosome alignment differs between meiosis I and meiosis II. In prometaphase
Telophase II and Cytokinesis
The chromosomes arrive at opposite poles and begin to
An animal cell with a diploid number of four (2n = 4) proceeds through the stages of meiosis to form four haploid daughter cells.
Possible NB Discussion Point
Have you ever enjoyed the convenience of a seedless fruit? If you’ve eaten the modern day banana, then you have consumed a triploid fruit. While the wild fruit is diploid and can sexually reproduce, seedless bananas arise from mutations, planned hybridizations, and can propagate asexually. Explain why triploid organisms are incapable of successfully undergoing meiosis. Can you think of any benefits to being triploid instead of diploid?
Comparing Mitosis and Meiosis
Mitosis and meiosis are both forms of division of the nucleus in eukaryotic cells. They share some similarities, but also exhibit distinct differences that lead to very different outcomes. Mitosis is a single nuclear division that results in two nuclei that
The main differences between mitosis and meiosis occur in meiosis I, which is a very different nuclear division than mitosis. In meiosis I, the homologous chromosome pairs become associated with each other,
When the chiasmata resolve and the tetrad
Meiosis II is much more analogous to a mitotic division.
Meiosis and mitosis are both preceded by one round of DNA replication; however, meiosis includes two nuclear divisions. The four daughter cells resulting from meiosis are haploid and genetically distinct. The daughter cells resulting from mitosis are diploid and identical to the parent cell.
The Mystery of the Evolution of Meiosis
Some characteristics of organisms are so widespread and fundamental that it is sometimes difficult to remember that they evolved like other simpler traits. Meiosis is such an extraordinarily complex series of cellular events that biologists have had trouble hypothesizing and testing how it may have evolved. Although meiosis
Meiosis and mitosis share obvious cellular
There are other approaches to understanding the evolution of meiosis in progress. Different
Link to Learning
Click through the steps of this interactive animation to compare the meiotic process of cell division to that of mitosis: How Cells Divide.
- Leigh Van Valen, “A new evolutionary law,” Evolutionary Theory 1 (1973): 1–30.
- Adam S. Wilkins and Robin Holliday, “The Evolution of Meiosis from Mitosis,” Genetics 181 (2009): 3–12.
- Marilee A. Ramesh,
Shehre-Banoo Malik and John M. Logsdon, Jr, “A Phylogenetic Inventory of Meiotic Genes: Evidence for Sex in Giardia and an Early Eukaryotic Origin of Meiosis,” Current Biology 15 (2005):185–91.