Meiosis and Mitosis Flashcards

(50 cards)

1
Q

How do eukaryotic cells reproduce? What are the general phases of this?

A

All cells have a cell cycle, which represents the life of a cell from the moment it is created from a parent cell until it divides to produce daughter cells (or dies).

The cell cycle consists of 2 consecutive, continuous phases: the mitotic (M) phase and interphase. Interphase involves 3 stages: G1, S and G2.

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2
Q

What is interphase? How long does it last? Can you see the chromosomes during this phase?

A

When a cell is in the mitotic phase it is undergoing cell division. By contrast, interphase is not considered part of cell division – rather preparatory.

Interphase sees the cell engaged in its normal metabolic activities whilst also preparing for its subsequent division by activities such as DNA replication and organelle duplication.

Approx 90% of a cell cycle is spent in interphase; for some adult mammalian cells this phase lasts for about 20 hours.

It is not usually possible to see individual chromosomes within the nucleus during interphase; this is only possible in the early mitotic stages once the genetic material has condensed.

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3
Q

What happens during interphase - G1 (first gap)

A

Cell recovers from previous division
Cell grows and increases in volume; high amount of protein synthesis
Organelles, such as the mitochondria and ribosomes are duplicated
Materials needed for DNA replication are accumulated
G1 checkpoint takes place to check that DNA is suitable for replication

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4
Q

What is interphase - S (synthesis)

A

DNA is replicated, resulting in two identical copies (or sister chromatids) of each chromosome joined at the centromere. Another name for replicated is synthesised, hence the name of the stage
Cell continues to grow and replicate organelles, the centrosome (in animal cells) is also duplicated
Specialised chromatin structures (such as sister-chromatid cohesions made from cohesin protein complexes) are constructed to prepare chromosomes for separated in M phase
S checkpoint to ensure DNA replication is complete

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5
Q

What is interphase - G2 (2nd gap)

A

Cell continues to grow and increase in volume; proteins required for chromosome manipulation are produced
Cytoskeletal filaments change; these will later aid in the movement of chromosomes during the mitotic phase and cell shape changes
G2 checkpoint takes place to check that DNA has replicated correctly

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6
Q

What is mitosis? What does it produce? What are the 5 stages?

A

Process by which one single cell divides to produce 2 genetically identical daughter cells. During mitosis, cells divide their nucleus and replicated chromosomes and their organelles before dividing their cytoplasm to form the 2 daughter cells.

There are 5 stages to mitosis: prophase, prometaphase, metaphase, anaphase and telophase. An additional stage of cytoplasmic division then occurs – cytokinesis.

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7
Q

What is prophase? (nucleolus, chromatins, centrosomes, mitotic spindle)

A

The nucleolus disappears, the nuclear envelope starts to fragment, and the DNA and associated proteins found within a cell, known as chromatins, start to coil up and condense.

The process of chromatin coiling up makes the DNA molecules more compact until they have condensed to a point at which they become visible through a light microscope.

During prophase, organelles called centrosomes (in animal cells) move to the opposite poles of the cell and make a series of long tubulin filaments, a form of microtubule. These microtubules are polar, with the minus ends embedded in the spindle pole in the centrosome and the plus ends pointing outward.

Collectively, these filaments form the mitotic spindle, the structure that will eventually be responsible for separating and moving the chromosomes into the new daughter cells.

Microtubules are dynamic polymers that constantly grow and shrink: this lengthening and shortening of the mitotic spindle is an essential element of cell division.

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8
Q

What is prometaphase? (kinetochores, cohesin)

A

Prometaphase follows prophase. During prometaphase, in cells other than fungal cells, the nuclear membrane breaks down fully, releasing DNA into the cytoplasm of the cell.

The microtubules produced during prophase now extend and attach to the chromosome centromeres at regions called the kinetochores in a process called search and capture.

The kinetochores feature molecular motor proteins that along with changes to the microtubules themselves, provide the pulling force to separate and move sister chromatids.

The size and complexity of kinetochores varies among different species. In higher eukaryotic cells they are multi-layered protein complexes that form at the centromere and can each bind 20-40 microtubules. Once these microtubules have attached to the kinetochores, the chromosomes can then begin the movement needed for the subsequent stages of mitosis.

During both prometaphase and metaphase (which follows), the chromosomes undergo dramatic structural changes as they condense, which help with their later separation.

Sister chromatids are held together by a type of protein called cohesin. During these stages, most cohesin complexes are lost from the arms, but remain at the centromeres. As a result, the centromeres become the only locations at which the chromatids are joined.

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9
Q

What is metaphase? What does the metaphase checkpoint?

A

Metaphase is the middle stage of mitosis, during which the replicated chromosomes line up along the equator of the dividing cell.

The spindle fibres which attached to the kinetochores of the replicated chromosomes during prophase, contract and relax and in doing so they draw the replicated chromosomes to the centre of the cell so that they line up along a region known as the metaphase plate.

Each sister chromatid is attached via the kinetochore to a spindle fibre. Sister chromatids are attached to spindle fibres that originate from opposite poles of the cells.

This arrangement of the chromosomes helps ensure that the 2 new daughter cells will each receive one copy of each of the chromosomes. A form of molecular ‘safety’ check called the metaphase checkpoint also confirms correct attachment of the kinetochores to the spindle, again to help ensure that the separation of chromosomes into the daughter cells happens as it should.

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10
Q

What is anaphase?

A

During anaphase, the replicated chromosomes are separated by cleavage of the cohesins that remain at the centromeres, through which the sister chromatids remain bound. Consequently, the sister chromatids are no longer physically associated.

The spindle fibre, which connect the kinetochores of the replicated chromosomes with one of the poles of the cell, shorten. Now that the chromosomes are no longer tethered to one another, the shortening of the spindle fibres pull them apart.

The spindle fibres continue to shorten, drawing the chromosome to which they are attached towards one of the poles of the cell. This ensures that each pole recieves the same kind and number of chromosomes as the original parent cell.

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11
Q

What is telophase?

A

By the time telophase is reached, the 2 complete sets of genetic information are situated at opposite poles of the dividing cell. During telophase these individual, separated chromosomes being to disperse and decondense, reforming the relaxed chromatin; at this point they are no longer visible under a light microscope.

A new nuclear membrane forms around each set of chromosomes and the spindle fibres disappear as they are dismantled. It may also be possible to see the cytoplasm of the cell starting to prepare for division during this stage.

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12
Q

What is cytokinesis?

A

Cytokinesis is the final stage of cell division, during which the cytoplasm is divided to produce the daughter cells. Cytokinesis proceeds differently in plant cells compared to animal cells.

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13
Q

How does cytokinesis occur in animal cells? (cleavage furrow)

A

In animal cells, a contractile ring of actin and myosin filaments forms around the centre of the cell, forming a cleavage furrow which becomes smaller in diameter until the cell is pinched into two, forming 2 daughter cells.

Each daughter cell contains a full complement of organelles and one nucleus with a complete set of chromosomes.

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14
Q

How does cytokinesis occur in plant cells?

A

Plant cells need to separate and rebuild a section of their cell wall, in addition to the cell membrane, to create daughter cells.

This rebuilding happens when modified vesicles from the golgi apparatus form across the previous cell plate until they eventually fuse together and with the plasma membrane. A new cell wall forms between these new membranes and division of the parent cell occurs.

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15
Q

When should mitosis occur? What is G0 state? How is mitosis triggered?

A

It is important that a cell undergoes mitosis only when new daughter cells are required. Mitosis should occur at the right time and in the right place. Normal, healthy eukaryotic cells will not undergo mitosis unless they receive signals, such as growth factors, telling them to grow and divide.

When they are not undergoing mitosis, cells exist in a non-dividing but viable state called G0. Mitosis can then be intiated by binding of growth factors to cell surface receptors, which span the plasma membrane. This binding triggers the activation of cell signalling pathways, which in turn trigger an increase in the amount of cyclin D proteins present.

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16
Q

What are D-type cyclins? What are checkpoints?

A

The D-type cyclins are members of one of 2 key groups of proteins that control the various stages of the cell cycle, and which also ensure that the stages occur in the correct order. The key regulatory proteins are the cyclin dependent kinases (CDK’s or CDC’s) and the cyclins.

Control is exerted at certain ‘checkpoints’ within the cell cycle. The checkpoints involves a combination of cyclins and CDKs although the identity of the proteins is specific to each checkpoint.

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17
Q

What happens at Checkpoint Restriction (R) or G1 to S

A

Checks for cell size, availability of nutrients, signals (positive growth cues), DNA damage
CDK 4,6,2
Cylin D, E

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18
Q

What happens at checkpoint G2?

A

Checks for DNA damage, DNA replication completeness
CDK 2
Cylcin A

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19
Q

What happens at checkpoint M?

A

Checks for chromosome attachment to spindle at metaphase plate
CDK 1
Cylin B

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20
Q

How do CDKs and cyclin binding partners work?

A

The cyclin-dependent kinases (CDKs) are inactive without a cyclin binding partner. So when the growth factor induced expression of the D cyclins raises their concentration, they can bind with either CDK 4 or 6.

CDK 4 and 6 are then able to phosphorylate their target proteins, ultimately leading to the transcription and expression of proteins required for DNA replication during S phase. Cyclin E is also epxpressed at this point, together with its partner CDK 2 it can help the cell to progress into S phase.

When DNA replication is completed, CDK 2 changes cyclin partner, from E to A. This results in a change of protein targets that CDK 2 can phosphorylate. For example, CDK2/cylinA phosphorylates a protein called DP1, causing it to be deactivated. DP1 is an important part of a transcription complex that helps drive S phase. So, by inhibiting this DP1 protein, S phase is brough to an end.

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21
Q

What do CDK 1 and cyclin B do?q

A

Further checks and DNA repair processes are carried out before the cell enters M phase. Here CDK 1 and cyclin B are important, particularly to check the correct attachment of chromosomes to the spindle. A single unattached kinetochore in the cell can block anaphase. The degradation of cyclin B is the signal for the final part of mitosis to occur.

22
Q

How do CDKs and cyclins change to ensure stages in the cell cycle occur in the correct order?

A

The various CDKs are present throughout the cell cycle, whereas the cyclins change in concentration, as their name implies. It is the sequential and cyclic increase and decrease in different cyclin proteins and their binding to the CDKs that ensures the various stages in the cell cycle occur in the correct order – for example that M phase or cell division only occurs after DNA replication in S phase and G2 has taken place.

The cyclins control the activity of their CDK binding partners. However, the progression and control of the cell cycle is not as simple as this. The CDKs need activating by being phosphorylated, and for any inhibitory phosphates being removed, before they can act on their targets.

23
Q

How are CDKs inhibited? What does this cause?

A

They are also subject to inhibition by families of proteins collectively known as the cyclon-dependent kinase inhibitors (CDKIs, also sometimes known as CKIs). Mutations in any of these important families of proteins (such as amplification or too much cyclin or CDK, or loss of one of the CDKIs) could result in mitosis occurring when it should not. This could lead to too many cells being produced, one key characteristic of a group of diseases known as cancers.

24
Q

What is the main error that can occur with mitosis?

A

Despite there being a number of checks to ensure cell division occurs correctly, the process can still go wrong. One problem that can occur is called non-disjunction, whereby the chromosomes fail to segregate properly. This results in the daughter cells receiving an incorrect number of chromosomes.

25
What is aneuploidy, monosomy and trisomy?
If the number of chromosomes in a cell is not an exact multiple of the haploid number, the cell exhibits a condition called aneuploidy. If only one copy of a chromosome is present – such that a whole chromosome is missing – the condition is referred to as monosomy. By contrast, if an additional chromosome is present the condition is termed trisomy, whereby a cell has 3 copies of a chromosome. These sorts of numerical chromosome aberrations can be observed in cancer cells (eg trisomy 12 in chronic lymphocytic leukaemia) alongside other structural changes to the chromosomes.
26
What is meisosis? What are haploid numbers?
The majority of animal and plant cells contain 2 complete sets of chromosomes within their nucleus, known as the diploid number of chromosomes. In humans this diploid number is 46 chromosomes, organised as 23 chromosome pairs. One of each of these chromosome pairs is inherited from the mother and one is inherited from the father. This means that for each gene that a diploid cell contains there are two copies of that gene. All organisms also contain some cells that possess only one copy of each chromosome, known as the haploid number of chromosomes. In animal cells, the only haploid cells are the gametes, the sperm and egg cells. When a sperm cell fuses with an egg cell during fertilisation, the two haploid gametes each pass on their single set of chromosomes so that the fertlised egg contains 2 full sets of chromosomes; it is diploid. Meiosis is a special form of cell division that occurs during the formation of gametes; gametes are sex cells (eg sperm, eggs and pollen)
27
Why do germline cells need different division from somatic cells?
The cells destined to become gametes (germline stem cells) undergo a different form of division from somatic cells (which only undergo mitosis) as they need to contain half the amount of genetic information that somatic cells contain: they need to be haploid rather than diploid. When fertilisation occurs during sexual reproduction, the 2 sets of haploid chromosomes – one set from the sperm and one from the egg (in case of non-plant reproduction) - come together so that the fertilised egg has a full quota of chromosomes: diploid. The reduction happens because meiosis comprises 2 nuclear divisions (meiosis I and meiosis II) to produce the haploid daughter cells. This is in contrast to the one division seen in mitosis.
28
Compare and contrast mitosis and meiosis?
Mitosis sees one diploid parent cell undergoing one nucleic division to produce two genetically identical daughter cells. The process of cell division is usually undertaken by somatic cells for growth of the organism, repair of damaged tissues or for sexual reproduction. By contrast, the process of meiosis involves one diploid parent cell undergoing two nuclear divisions, the first being a reduction division, the final objective being to produce 4 genetically different haploid daughter cells. This process is undertaken by eukaryotic organisms during the production of gametes.
29
What happens in meiosis I? What is the main event and why is it important?
Meiosis I is a reduction division; it separates the homologous pairs of chromosomes and in doing so, halves the number of chromosomes within the resulting daughter cells. It is also during this division that recombination (crossing over) occurs, leading to an increase in genetic variation.
30
What happens in meiosis II?
By contrast, meiosis II occurs in a similar manner to mitosis: replicated chromosomes (sister chromatids) separate and move into the final daughter cells (in this case, the gametes).
31
What is the main difference between genetic material in mitosis and meiosis?
This process of meiosis also differs from mitosis because it allows the alleles to be swapped between similar chromosomes during a process known as crossing over. This introduces genetic variation during the process of gamete production and is central to the differences exhibited by offspring compared with their parents.
32
What happens during the meiotic S phase?
Before meiosis can begin the meiotic S phase takes place, during which the DNA is replicated and the chromosomes are loaded with a meiosis-specific cohesin complex, which keeps the sister chromatids together until anaphase of meiosis II.
33
What happens in prophase I? (Bivalent synapsis, synapsis, synaptonemal complex, chiasmata, post-synapsis homologous)
As with the prophase seen during mitosis, prophase I of meiosis sees the nucleolus disappear, microtubules that will form the spindle begin to form and there is coiling up and condensing of the chromatin. While this occurs, the proteins that help to form these condensed chromosomes bring the members of each homologous pair (bivalent) close together; this tight pairing is called a synapsis. During synapsis, the two members of a homologous pair are precisely lined up with each other so that the corresponding genes on each chromosome align. The homologous pair are initially linked tightly together along their entire length by a protein scaffold for the synaptonemal complex to bind to. This tight interaction between the homologous pairs means that sections of non-sister chromatids may exchange with each other through a process known as crossing over. These sites of crossing over are seen visually as chiasmata (singular: chiasma) as the synaptonemal complex dissolves. The number of chiasmata varies with the length of the chromosome involved and the species of organism Post-synapsis homologous chromosomes contain different combinations of genetic information to each other and to the original parent chromosomes. These individuals chromatids, which carry genetic information from both the paternal and maternal chromosomes, known as recombinants. Crossing over recombines the genetic information found in the homologous pairs of chromosomes in many different ways. As such, it is a fundamental way of introducing diversity to any population of sexually reproducing organisms.
34
What is prometaphase I?
As the stage of prophase I continues into prometaphase I, the homologous pairs of chromosomes are no longer as closely associated to eachother: they are held together only by the chiasmata. The microtubules that form the spindle fibres connect to the kinetochores of the homologous chromosomes as well as the poles of the cell. By this stage, the nuclear membrane of the cell has fully broken down so that the spindle fibres are able to move the chromosomes within the cell.
35
What is metaphase I? What is the key event?
As the cell progresses to metaphase I, the spindle fibres contract and relx in sequence until the homologues are lined up across the equator of the cell. The pairs are orientated randomly across the centre of the cell with the kinetochores on either side facing opposite poles. This random arrangement of the homologous pairs is known as independent assortment; it is another fundamental process that results in genetic variation within populations. When considering the combined effect of both crossing over and independent assortment in terms of variation introduced, it becomes extremely unlikely that any two haploid gametes resulting from meiosis will contain identical genetic information.
36
What is anaphase I?
During anaphase I, contraction of the spindle fibres separates the homologues (the chiasmata are broken) and draws them towards the opposite poles of the cell. At this point the genetic material still takes the form of a pair of replicated sister chromatids joined together at the centromere by cohesin proteins. This is different to mitosis where the sister chromatids are separated during anaphase.
37
What is anaphase I?
During anaphase I, contraction of the spindle fibres separates the homologues (the chiasmata are broken) and draws them towards the opposite poles of the cell. At this point the genetic material still takes the form of a pair of replicated sister chromatids joined together at the centromere by cohesin proteins. This is different to mitosis where the sister chromatids are separated during anaphase.
38
What is telophase I?
The final stage of the first meiotic division is telophase I. During telophase the spindle fibres that complete the movement of the replicated chromosomes so that each pole of the parent cell contains one full set of replicated chromosomes; although there are sister chromatids at this point, it is considered a haploid set. Around each set of chromosomes, a nuclear envelope may reform, and the chromosome may decondense (depending on the species). The microtubules that had formed the spindle disappear.
39
What happens during cytokinesis in meiosis?
Cytokinesis then occurs in the same manner as described for mitosis. This time, 2 non-identical daughter cells are formed.
40
What happens during meiosis II?
Meiosis II starts with each of the daughter cells from meiosis I containing chromosomes made up of 2 sister chromatids joined together at the centromere. By the end of the second meiotic division there will be 4 non identical haploid daughter cells.
41
What happens during prophase II?
Prophase II starts with chromosomes condensing again (if they condensed in telophase I) and with the nuclear membrane fragmenting (if it had reformed during telophase I). As seen with the prophase stages of other cell divisions, the centrosomes move towards the opposite poles of the cell and the spindle fibre microtubules reform.
42
What happens during prometaphase II? What happens during anaphase II?
By prometaphase II, the nuclear envelopes have completely disintegrated and meiotic spindle in each cell is fully formed. The microtubules of the spindle attach to kinetochores of each of the sister chromatids to link them to the centrosomes at each pole of the cell. Once again, the spindle fibres contract and relax to manoevre the sister chromatids to the equator of the cell, where they line up prior to being pulled apart by the action of the spindle fibres in anaphase II.
43
What happens in telophase II and cytokinesis?
The sister chromatids which are now separate, migrates towards the opposite poles of the cells such as by telophase II, each pole the cell contains a single haploid set of chromosomes. Once again, a nuclear envelope forms around the haploid set of chromosomes and cytokinesis takes place. Each of the four daughter cells produced as a result of the two divisions of meiosis is genetically different to the others and to the original parent cell.
44
How is meiosis controlled?
A number of regulatory controls points also operate during the production of the haploid gametes to both initiate meiosis and to regulate the various steps through the 2 cells divisions.
45
What has to happen in order for meiosis to take place in males and females?
The germline stem cell first has to leave the mitotic cell cycle and enter the meiotic cell cycle (a step called the mitosis/meiosis decision). In the female mammalian species (including humans), meiosis starts just a few months after conception in the fetal ovary. Meiosis is then halted at metaphase II until the individual reaches puberty, when one or a few of the oocytes are released from the ovary at a time. If the oocyte then meets a sperm, meiosis is completed and fertilisation occurs. In males, in contrast, meiosis is all postnatal.
46
What is the main controller of both mitosis and meiosis? What part of meiosis requires specific regulation?
The basic cell cycle machinery responsible for the control of the mitotic cell cycle (the CDKs and cyclins) is also in control of the main steps of the meiotic cell cycle. However, the lack of an S phase between meiosis I and II and the recombination events requires specific regulation. The overall frequency of recombination as well as crossing over at particular region of the chromosomes is regulated.Additional checkpoints, such as the meiotic recombination checkpoint are present to ensure recombination is complete. If not, meiotic division is arrested or delayed, thus preventing the formation of defective gametes. Other steps of meiosis such as chromosomes separation are regulated.
47
What are inherited diseases from errors in meiosis the result of?
Errors that arise during meiosis can result in inherited diseases. These can be a result of numerical aberrations (too many or too few chromosomes, aneuploidy) or structural changes to the chromosomes (including partial duplications, deletions, inversions and translocations).
48
What is aneuploidy?
Aneuploidy is often the result of a failure of the chromosomes to segregate properly during meiosis I or II, a phenomenon known as non-disjunction. Aneuploidy is thought to be quite common, with about 5 percent of all conceptions being monosomic or trisomic. Most however are lethal, with aneuploidy being a leading cause of miscarriage.
49
What are monosomes and trisomies and give an example of a condition for each?
In animals, monosomies only result in live births when one of the sex chromosomes is lost (example being turner syndrome in humans/females). Trisomies are more common, with either a sex chromosome being duplicated (eg Klinefelter syndrome, an additional x chromosome in men) or one of the autosomes – 13, 15, 18, 21 or 22 – being involved.
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