Meiosis Flashcards
(34 cards)
Background:
Chromosomes in cells that are not dividing.
Chromosomes:
- Exist as single-stranded structures intertwined to form the chromatic network.
- Occur in homologous pairs called a bivalent. One chromosome of each pair comes from the mother and one comes from the father.
- Homologous - chromosomes that are similar in many ways such as position and structure
- Replicate during the interphase of a cell cycle, ie between cell divisions, to form two identical chromatids (sister chromatids). These are joined by a centromere. This takes place before cells divide by either mitosis or meisos.
- Centromere - a specialized constricted region of a choromosome where the two chromatids are held together and to which spindle fibers attach during cell division.
- Only become visible when the chromosomes shorten and thicken as a cell divides.
Meiosis
Meiosis is a special type of cell division that takes place in the reproductive organs of plants and animals to produce gametes (sex cells) in animals and spores in plants.
Cells divide by mitosis. Mitosis enables organisms to grow and to replace tissue. In mitosis replication is followed by one division. In meiosis, replication is followed by two divisions.
- Meiosis 1 is a reduction division which results in two cells being formed each with half the number of chromosomes of the parent cell, ie the haploid (n) number.
- Meiosis 2 is a copying division which involves two haploid cells formed, each dividing again by mitosis to form four daughter haploid cells.
Meiosis 1: Reduction Division
The first division separates the homologous chromosomes into two intermediate cells.
Meiosis 1: Early Prophase 1
As in mitosis, the chromosomes condense, becoming short and fat. They are visible as two chromatids joined by a centromere. From here on the behaviour of the chromosomes in meiosis 1 differ from that in mitosis.
Meiosis 1: Late Prophase 1
- The chromosomes of homologuous pairs lie alongside one another in a process called synapsis to form bivalents.
- The centrioles move to opposite poles.
- A spindle, made up of protein threads, develops across the cell to form the two centrioles. Centrioles are minute rod-shaped bodies formed from the centrosome.
- The nuclear membrane breaks down.
- Parts of the chromatids can become entangled and exchange segments of chorosomes in a process called crossing over.
Meiosis 1: Metaphase 1
- the bivalents (not single chromosomes) move to the middle of the cell and line up on the equator in a way that is completely random.
- The centromeres become attached to the spindle treads.
- The centromeres do not split.
Meiosis 1: Anaphase 1
- The bivalents separate and the homologues are pulled away from each other by contracting spindle threads. This results in independent assortment of maternal and paternal chromosomes. One chromosome of each pair moves to the opposite pole.
Meiosis 1: Telophase 1
The cytoplasm then divides (cytokineses) to form two haploid cells, both of which have only one of each homologous pair of chromosomes.
Meiosis 2: A Copying Division
Each of the haploid cells will divide again by mitosis so that the chromatids are pulled apart but the number of chromosomes remains the same. This produces a large number of gametes.
Meiosis 2: Late Prophase 2
Each chromosome is made up of two chromatids joined by a centromere. The centriole divides, forming two centrioles. A spindle develops between the centrioles which move to opposite poles. The nuclear membranes dissapears.
Meiosis 2: Metaphase 2
The chromosomes move to the middle of the cell where they line up at the equator. The centromeres become linked to the spindle threads.
Meiosis 2: Anaphase 2
The centromeres split, allowing each chromosome to separate into two chromatids. Spindle threads contract and pull the chromatids apart. The chromatids, which are now called daughter chromosomes, move to opposite ends (poles) of the cell.
Meiosis 2: Telophase 2
Daughter chromosomes group together at the poles. A new nuclear membrane starts to form around each set of daughter chromosomes.
Meiosis 2: Cytokinesis
The cytoplasm starts to divide forming two new daughter cells, each with the haploid numbers of chromosomes. This process is called cytokineses. A new nucleus forms and the daughter chromosomes form the chromatin network.
At the end of meisos, four new, non-identical, haploid gametes are formed from one parent cell, each with half the original number of chromosomes. The gametes are not identical to the parent cell.
Meiosis: To sum up:
- Two chromatids make up a chromosome.
- Two chromosomes make up a homologous pair.
- A pair of homologous chromosomes makes up a bivalent.
What is crossing over?
Crossing over is the mutual exchange of pieces of chromosome so that whole groups of genes are swapped between maternal and paternal chromosomes. This takes place in late prophase to early metaphase of meiosis 1.
- This replicated homologous pairs of chromosomes come together in a process called synapsis to form bivalents. They swap pieces of their inner chromatids by breaking and rejoining their DNA while they ate paired up.
- The points of crossing over where the chromatids break are called chiasmata. In this way, some genes from a maternal chromatic change place with some genes from a paternal chromatid, forming a recombinant chromatid. Recombinants will result in offpspring with genotypes unlike either parent. The outer, unchanged chromatids are called parentals.
- Only one charisma is shown by many may occur per pair of chromosomes.
Why is crossing over important?
- The exchange of genetic material produces chromatids with a unique combination of genes. This increases genetic variation among individuals in a population. This is why offspring do not look the same.
- During this exchange process, mistakes may occur which lead to mutations. Most mutations are harmful but occasionally they may be beneficial. New genes may be introduced into the genetic code of a species which is important in the process of evolution as it provides the raw material on which natural selection acts.
- Crossing over guarantees the individual characteristics of each one of us.
Purposes of Reduction Division
The cells making up the body of an organism are called somatic cells and in most organisms these cells contain two sets of chromosomes, ie they are diploid (2n).
One set is inherited from the mother and the other from the father. In humans, the diploid number is 46 chromosomes.
- Meiosis is called a reduction division as, during the first meiotic division, the number of chromosomes is reduced from two sets (diploid) in the parent cell to one set (haploid) in each of the daughter cells (gametes) formed. In humans the haploid number is 23 chromosomes.
- Gametes or sex cells in diploid organisms, ie most animals and seed-bearing plants, are made by meiosis so that the number of chromosomes is halved. This process is called gametogenesis. In animals the:
- Formation of sperm - spermatogenesis, occurs in the testes
- Formation of egg cells - oogenesis, occurs in the ovaries
In Angiosperms (flowering plants) meiosis takes place in the anthers and ovaries to produce haploid gametes.
How do Mosses and Ferns differ?
An exception is found in primitive plants such as mosses and ferns where haploid spores are formed by meiosis in a diploid sporophyte generation. The spores develop into a haploid gametophyte plant. Specialized cells in the male and female organs of this plant produce haploid gametes by mitosis. On fertilization the zygote develops into a diploid sporophyte.
Importance of Meiosis
- Gametes are formed by the process of meiosis.
- During meiosis the number of chromosomes is halved so that the chromosome number is kept constant from generation to generation.
- Meiosis results in genetic variation through:
- Crossing over
- Random arrangement of chromosomes at the equator of the cell during metaphase.
The number of chromosomes in a cell is characteristic of an organism, eg humans have 46 chromosomes.
Genetic Variation:
In organisms which reproduce sexually every one of the offspring possess a unique combination of genes, ie in sexual reproduction there is always variation.
Variation - the differences which exists between organisms belonging to the same species.
This variation of the offspring is caused by differences in their genetic code as a result of:
- The crossing over of pieces of chromatids, which causes a reshuffling of the genes in the gametes formed.
- The random lining up of maternal and paternal chromosomes on the equator of the cell during metaphase of meiosis. This is called the independent assortment of chromosomes and it results in every egg and every sperm formed containing a mixture of maternal and paternal chromosomes.
A single set of chromosomes in a human sperm or egg could consist of 17 maternal and 6 paternal or 14 paternal and 9 maternal etc.
- The sheer chance as to which particular sperm fertilizes an egg cell during fertilization. The new individual will have a unique combination of genes, different from either of its parents, and different from any other offspring produced by the same parents.
- Mutations, which are sudden and unpredictable changes in the genetic code of an organism.
Abnormal Meiosis
Chromosome non-disjunction is a form of abnormal meiosis as the chromosomes fail to separate correctly.
The consequences of non-disjunction:
If this occurs during meiosis in the formation of sex chromosomes, an egg cell or sperm an be formed with two X’s, two Ys or with neither an X or Y chromosome.
If this occurs during meiosis in autosomal pairs, fertilisation involving one of these abnormal pairs, fertilisation involving one of these abnormal gametes results in a zygote with either an extra or missing chromosome - a condition called aneuploidy.
Aneuploidy causes various physical and mental characteristics called clinical syndromes.
Polypoidy is a condition in which an organism (mainly plants) has more than two complete sets of chromosomes in a cell.