Cell Cycle & Mitosis Flashcards
What are some key characteristics that all mammals share?
- Milk producing mammary glands
- three bones in the middle ear and one in the lower jaw
- fur or hair
- heterodont dentition (different kinds of teeth)
- both SEBACEOUS (oil-producing) and SUDORIFEROUS (sweat) glands
What are the two groups of mammals that birth their young differently?
- PROTOTHERIANS
* METATHERIANS
What are prototherians? How do they give birth?
- Also known as MONOTREMES and include the duck-billed platypus and echidna (spiny anteater)
- These mammals encase their developing embryos within hard-shelled amniotic eggs and lay them to be hatched, like reptiles
- This method of development is referred to as OVIPARITY
What are metatherians and how do they give birth?
- Metatherians, also known as MARSUPIALS, include koalas and kangaroos
- A typical meteatherian fetus undergoes SOME development in its mothers uterus and then climbs its way out of the birth canal and into her marsupium, or POUCH
In animals, what is the difference between autosomal cells and germ cells?
- Autosomal cells are said to be DIPLOID (2n), which means that they contain two copies of each chromosome
- GERM CELLS are HAPLOID (n), containing only one copy of each chromosome
- In humans, 2n=46, and n=23, meaning that we inherit 23 chromosomes from each parent
Generally, what is the cell cycle?
*EUKARYOTIC cells replicate through the cell cycle, a specific series of phases during which a cell GROWS, synthesizes DNA, and DIVIDES.
For actively dividing cells, the cell cycle consists of FOUR stages: G1, S, G2, and M.
Derangement of the cell cycle can lead to unchecked cell division, and may be responsible for the formation of cancer.
What is interphase in the cell cycle?
- The first three stages (G1, S, and G2) are known as INTERPHASE
- Interphase is the longest part of the cell cycle, even actively dividing cells spend about 90% of their time in interphase
What is the G0 part of the cell cycle?
- Cells that do NOT divide spend all of their time in an OFFSHOOT of G1 called G0
- During the G0 stage, the cell is simply living and serving its function, without any preparation for division
What is the difference between the configuration of DNA during interphase vs. during mitosis, and why?
- During INTERPHASE, individual chromosomes are not visible with LIGHT MICROSCOPY because they are in a less condensed form known as CHROMATIN. This is because the DNA must be available to RNA polymerase so that genes can be TRANSCRIBED
- During MITOSIS, however, it is preferable to condense the DNA into tightly coiled chromosomes to avoid losing any genetic material during cell division
What happens during the G1 phase? What happens at the END of the G1 phase?
- During the G1 phase, also known as the pre-synthetic GAP, cells create organelles for energy and protein production (mitochondria, ribosomes, and endoplasmic reticulum), while also increasing their size
- Passage into the S (synthesis) stage is governed by a RESTRICTION POINT
- In order to pass the restriction point, certain criteria, like containing the proper complement of DNA, must be met for the cell to pass the restriction pint and enter the next stage
What happens during the S stage?
- During the S phase, the cell REPLICATES ITS GENETIC MATERIAL so that each daughter cell will have identical copies
- After replication, each chromosome consists of two identical CHROMATIDS that are bound together at specialized regions known as the CENTROMERE
- The PLOIDY of the cell does NOT change even though the number of chromatids has doubled. Humans in this stage still only have 46 chromosomes, even though 92 chromatids are present
- Cells entering G2 have TWICE as much DNA as cells in G1
What does PLOIDY mean?
- Ploidy is the number of sets of chromosomes in a cell
- Usually a gamete (sperm or egg) carries a full set of chromosomes that include a single copy of each chromosome
- The gametic or haploid number (n) is the number of chromosomes in a gamete
- Two gametes form a DIPLOID ZYGOTE with twice this number (2n), meaning there are two copies of autosomal chromosomes
- For humans, a diploid species, n=23; this means a typical human somatic cell contains 46 chromosomes, composed of 2 complete haploid sets, which makes up 23 HOMOLOGOUS CHROMOSOME PAIRS
- Cells are described according to the number of chromosome sets present, known as the ploidy level: monoploid (1 set), diploid (2 set), tetraploid (4 set), etc.
What does chromatid mean? What about chromosome?
- Each chromatid is composed of a COMPLETE, double-stranded molecule of DNA
- Sister chromatids are IDENTICAL COPIES of each other
- CHROMOSOME may be used to refer to either a SINGLE CHROMATID before S phase or the PAIR of chromatids attached at the centromere after S phase
What happens during G2 phase?
- Also known as the POSTSYNTHETIC GAP
- During G2 phase, the cell passes through another quality control checkpoint
- DNA has already been dupliciated, and the cell checks to ensure that there are enough organelles and cytoplasm to divide between the two daughter cells
- The cell also checks to make sure that DNA replication proceeded CORRECTLY to avoid passing on an ERROR to daughter cells that may further replicate the error in their PROGENY
What happens during M stage (MITOSIS)?
*The M stage consists of MITOSIS itself along with CYTOKINESIS
*Mitosis is divided into four phases: prophase, metaphase, anaphase, and telophase
8Mitosis is the process by which TWO IDENTICAL daughter cells are created from a SINGLE CELL
*Mitosis occurs in SOMATIC CELLS, or cells that are NOT involved in sexual reproduction
*Cytokinesis is the SPLITTNG of the cytoplasm and organelles into two daughter cells
What is the difference between division in autosomal cells vs. germ cells?
- In autosomal cells, division results in TWO genetically identical daughter cells
- In germ cells, the daughter cells are NOT EQUIVALENT
What is the cell checking for at the G1/S checkpoint? What happens if the conditions to pass the checkpoint are not met?
- The cell is looking to see if the DNA is in good enough condition for SYNTHESIS
- This checkpoint is also known as the restriction point
- If there has been damage to the DNA, the cell cycle goes into arrest until the DNA has been repaired
- The main protein in control of this is known as p53
What is the cell checking for at the G2/M checkpoint?
- At this checkpoint, the cell is mainly concerned with ensuring that the cell has achieved adequate SIZE and the organelles have been properly replicated to support two daughter cells.
- P53 also plays a role here
What are the molecules responsible for the cell cycle?
- The molecules responsible for the cell cycle are known as CYCLINS and CYCLIN-DEPENDENT KINASES (CDK)
- In order to be activated, CDK’s require the right kind of cyclins to be present
- During the course of the cell cycle, concentrations of various cyclins increase and decrease during specific stages. These cyclins BIND to CDK’s, creating an activated CDK-cyclin complex
- The CDK-cyclin complex can then PHOSPHORYLATE transcription factors, and these transcription factors THEN promote transcription of genes required for the next stage of the cell cycle
What happens when the p53 gene, called TP53, is mutated?
- CANCER
- One of the most COMMON mutations found in cancer is mutation of the gene that produces p53, called TP53
- When this gene is mutated, the cell cycle is NOT stopped to repair damaged DNA, which allows for mutations to accumulate, eventually resulting in a CANCEROUS CELL that divides CONTINUOUSLY and without regard to the quality or quantity of the new cells produced
- Cancer cells will often rapidly divide, creating TUMORS
What is metastasis and how can it happen?
- If a cancerous cell (i.e. a cell with a mutated p53 gene) begins to produce the right factors, like proteases that can DIGEST basement membranes or factors that encourage blood vessel formation, the damaged cells are then able to reach other tissues
- This may include LOCAL invasion as well as DISTANT spread of cancerous cells throughout the bloodstream or lymphatic systems
- Metastasis is when the cancerous cells spread throughout the body
What are the two main kinds of cancer causing genes?
- ONCOGENES: genes that, when mutated, ACTIVELY promote cell division
- TUMOR SUPRESSOR GENES: genes that, when mutated, lose their ability to regulate or pause the cell cycle
- Different cancer types are often associated with specific mutations in either ONCOGENES or TUMOR SUPRESSOR GENES or BOTH
What happens during prophase?
o Prophase is the FIRST phase in mitosis
o First step in prophase involves CONDENSATION of the chromatin into CHROMOSOMES
o The centriole pairs separate and move toward opposite poles of the cell; these paired cylindrical organelles are located OUTSIDE the nucleus in a region known as the CENTROSOME and are responsible for the correct division of DNA
o Once the centrioles migrate to opposite poles of the cell, they begin to form SPINDLE FIBERS, which are made of microtubules
o Each of the spindle fibers radiate outward from the centrioles
o Some microtubules form ASTERS that anchor the centrioles to the cell membrane while others extend toward the middle of the cell
o The NUCLEAR MEMBRANE also dissolves during prophase, allowing the spindle fibers to make contact with the chromosomes
o The nucleoli becomes less distinct and may disappear completely
o Kinetochores appear at the centromere
What are kinetochores?
*Kinetochores are protein structures located on the centromeres that serve as attachment points for specific fibers of the spindle apparatus appropriately called kinetochore fibers
In general, what happens during each phase of mitosis to the chromosomes?
- Prophase: chromosomes CONDENSE, spindle apparatus forms
- Metaphase: chromosomes ALIGN
- Anaphase: sister chromatids separate
- Telophase: new nuclear membranes form
What happens during METAPHASE?
- During metaphase, the centriole pairs are now at opposite ends of the cell
- The kinetochore fibers interact with the fibers of the spindle apparatus to align the chromosomes at the metaphase plate (equatorial plate), which is equidistant between the two poles of the cell
What happens during anaphase?
- During anaphase, the centromeres SPLIT so that each chromatid has its own distinct centromere, thus allowing the sister chromatids to separate
- The sister chromatids are pulled toward the opposite poles of the cell by the shortening of the kinetochore fibers
What happens during telophase?
- Telophase is the reverse of prophase
- The spindle apparatus disappears
- A nuclear membrane reforms around each set of chromosomes, and the nucleoli reappear
- The chromosomes uncoil, resuming their interphase form
- Each of the two new nuclei has received a complete copy of the genome identical to the original genome and to each other
What is cytokinesis?
*At the end of telophase, cytokinesis is the separation of the cytoplasm and organelles so that each daughter cell has sufficient supplies to survive on its own
Typically how many times do human cells divide?
- Each cell undergoes a finite number of divisions before programmed death
- For human somatic cells, this is usually between 20 and 50
- After that, the cell can no longer divide continuously
Where does meiosis occur and what generally is it?
Meiosis occurs in gametocytes (GERM CELLS) and results in up to four nonidentical sex cells (GAMETES)
What are some similarities between meiosis and mitosis? What are some general differences?
SIMILARITIES: In both processes, genetic material must be duplicated, chromatin is condensed to form chromosomes, and microtubules emanating from centrioles are involved in dividing genetic material.
DIFFERENCES: mitosis consists of one round of replication and division while meiosis consists of one round of replication followed by TWO rounds of division
What are the two rounds of division in meiosis?
Meiosis I: results in homologous chromosomes being separated, generating haploid daughter cells (REDUCTIONAL DIVISION)
Meiosis II: similar to mitosis, in that it results in the separation of sister chromatids (EQUATIONAL DIVISION)
What is the difference between homologous pairs and sister chromatids?
The human genome is composed of 23 HOMOLOGOUS PAIRS of chromosomes (homologues), each of which contains ONE chromosome inherited from each parent.
Homologous pairs are considered SEPARATE CHROMOSOMES (i.e. material chromosome 15 and paternal chromosome 15).
SISTER CHROMATIDS are IDENTICAL STRANDS of DNA connected at the centromere.
After S Phase, there are 92 chromatids organized into 46 chromosomes, which are organized into 23 homologous pairs.
What happens during prophase I of meiosis? Specifically what is the state of the genetic information?
The chromatin condenses into CHROMOSOMES, the spindle apparatus forms, and the nucleoli and nuclear membrane disappear.
Homologous chromosomes come together and intertwine in a process called synapsis. Each chromosome consists of TWO SISTER CHROMATIDS, so each synaptic pair contains FOUR chromatids & is referred to as a tetrad.
What first major difference between meiosis and mitosis occurs during prophase I of meiosis?
HOMOLOGOUS CHROMOSOMES come together and intertwine in a process called SYNAPSIS.
What is the process of CROSSING OVER that often occurs during prophase I of meiosis?
Chromatids of homologous chromosomes may break at the point of synapsis, called the CHIASMA and exchange equivalent pieces of DNA, a process known as crossing over.
Crossing over occurs between HOMOLOGOUS chromosomes and NOT between sister chromatids of the same chromosome (sister chromatids are identical so crossing over wouldn’t produce any change)
Result of crossing over is an altered but structurally COMPLETE set of genes. Genetic recombination like crossing over can unlink linked genes, thereby increasing the variety of genetic combinations that can be produced via gametogenesis.
What does linkage mean in regards to genes?
Linkage refers to the tendency for genes to be inherited TOGETHER; genes that are located further from each other physically are less likely to be inherited together, and more likely to undergo crossing over relative to each other.
Why is genetic recombination a benefit in sexual reproduction, and how does this compare to asexual reproduction?
ASEXUAL reproduction produces IDENTICAL OFFSPRING.
Sexual reproduction provides the ADVANTAGE of GREAT GENETIC DIVERSITY, which is believed to increase the ability of a species to evolve and adapt to a changing environment.
Chiasma
A point at which paired chromosomes remain in contact during the first metaphase of meiosis, and at which crossing over and exchange of genetic material occur between the strands.
How can the distance between two genes on a chromosome be determined?
THE RATE of gene unlinking can be used to map differences between two genes on the same chromosome.
The farther apart two genes are, the more likely they are to become UNLINKED during crossing over. These statistics can then be used to determined the distance between genes on the chromosome, measured in units called CENTIMORGANS.
How does crossing over explain Mendel’s second law of independent assortment?
Mendel’s second law states that the INHERITANCE of one allele has no effect on the likelihood of inheriting certain alleles for other genes. It states that the alleles of one gene sort into the gametes independently of the alleles of another gene.
Because of crossing over, each daughter cell will have a UNIQUE POOL OF ALLELES (genes coding for alternative forms of a given trait) from a random mixture of maternal and paternal origin. Genes that are on the same chromosome can be inherited together, but crossing over during meiosis may separate them.
The principle or law of independent assortment is applicable to only those factors or genes which occur on different chromosomes. Actually, a chromosome bears hundreds of genes. All the genes or factors present on a chromosome are inherited together except when ‘crossing over’ takes place.
Why is Mendel’s Second Law not always valid for two or more phenotypical traits of an individual?
Mendel’s Second Law, or the law of the independent assortment, is valid for genes located in different chromosomes. These genes segregate independently during meiosis.
However, Mendel’s Second Law is not valid for phenotypical features conditioned by genes located in the same chromosome (genes under linkage), since these genes, known as linked genes, do not separate during meiosis (except for the phenomenon of crossing over).
What happens during metaphase I of meiosis?
During metaphase I, homologous pairs (TETRADS) align at the metaphase plate, and each pair attaches to a separate spindle fiber by its kinetochore.
How is metaphase I in meiosis distinct from metaphase in mitosis?
In mitosis, each CHROMOSOME is lined up on the metaphase plate by two spindle fibers (one from each pole–each spindle fiber connects to one sister chromatid)
In Meiosis, homologous chromosomes are lined up across from each other at the metaphase plate and held by ONE spindle fiber. (each chromosome is attached to one spindle fiber so the homologous chromosomes themselves can be separated)
What happens during anaphase I of meiosis?
During anaphase I, homologous pairs SEPARATE and are pulled to opposite poles of the cell–a process called DISJUNCTION and it accounts for Mendel’s FIRST LAW of segregation.
During disjunction, each chromosome of paternal origin separates (disjoins) from its homologue of maternal origin (so homologous pair separates), and either chromosome can end up in either daughter cell depending on how the homologous pair arranged on the metaphase plate. The distribution of homologous chromosomes to the two intermediate daughter cells is random with respect to parental origin. The separating of two homologous chromosomes is referred to as segregation.
How is meisis different from mitosis?
The chromosome number is HALVED (reductional division) in meiosis I, and the daughter cells produced have the HAPLOID number of chromosomes (23 chromosomes in humans), and each chromosome in the daughter cells is composed of two chromatids (sister chromatids), which are identical.
How is meiosis II similar to mitosis?
Sister chromatids are SEPARATED from one another so no change in ploidy is observed.
What happens during telophase I of meiosis?
During telophase I, a nuclear membrane forms around each new nucleus. Each chromosome still consists of TWO SISTER CHROMATIDS joined at the centromere.
The cells are now HAPLOID: once homologous chromosomes separate, only n chromosomes are found in each daughter cell (23 in humans).
The cell divides into two daughter cells by CYTOKINESIS. Between cell divisions, there may be a short REST period (INTERKINESIS) during which the chromosomes partially uncoil.
What happens if during either anaphase I or anaphase II of meiosis the homologous chromosomes (anaphase I) or sister chromatids (anaphase II) fail to separate?
One of the resulting gametes will have TWO copies of a particular chromosome and the other gamete will have NONE.
Subsequently during fertilization, the resulting ZYGOTE may have TOO MANY or TOO FEW copies of that chromosome.
Nondisjunction can affect bboth autosomal chromosomes (trisomy 21) and sex chromosomes (Klinefelter’s or Turner syndromes)
What happens during meiosis II?
Meiosis II is really similar to mitosis as sister chromatids (not homologues) are separated from each other.
What happens during prophase II?
The nuclear envelope dissolves, the nucleoli disappear, the centrioles migrate to opposite poles, and the spindle apparatus forms.