Meiosis (DP IB Biology)

Meiosis as Reduction Division

• There are two processes by which the nucleus of a eukaryotic cell can divide. These are:

  • Mitosis

  • Meiosis

• Mitosis gives rise to genetically identical cells and is the type of cell division used for growth, repair of damaged tissues, replacement of cells and asexual reproduction

• Meiosis gives rise to cells that are genetically different from each other and is the type of cell division used to produce gametes (sex cells)

• During meiosis, the nucleus of the original 'parent' cell undergoes two rounds of division. These are:

  • Meiosis I

  • Meiosis II

Meiosis I

• The nucleus of the original 'parent' cell is diploid (2n) i.e. it contains two sets of chromosomes

• Before meiosis I, these chromosomes replicate

• During meiosis I, the homologous pairs of chromosomes are split up, to produce two haploid (n) nuclei

  • At this point, each chromosome still consists of two chromatids

• Note that the chromosome number halves (from 2n to n) in the first division of meiosis (meiosis I), not the second division (meiosis II)

  • This is why the first division of meiosis is also known as reduction division

• During prophase I of meiosis homologous chromosomes pair up and are in very close proximity to each other

  • A pair of homologous chromosomes can be referred to as a bivalent

  • At this point, there can be an exchange of genetic material (alleles) between non-sister chromatids in the bivalent

    • The crossing points are called chiasmata

  • This results in a new combination of alleles on the two chromosomes (these can be referred to as recombinant chromosomes)

  • This exchange of genetic material is known as crossing over

• Spindle fibres attach to the centromeres of the bivalents which pulls the homologous chromosomes to the opposite poles of the cell

  • The individual chromatids of each chromosome are still attached by their centromeres

• Between meiosis I and II there is no replication of the chromosomes

Meiosis II

• During meiosis II, the chromatids that make up each chromosome separate to produce four haploid (n) nuclei

  • At this point, each chromosome now consists of a single chromatid

Meiosis overview diagram

One diploid nucleus divides by meiosis to produce four haploid nuclei

The need for meiosis in a sexual life cycle

• The life cycles of organisms can be sexual or asexual (some organisms are capable of both)

  • In an asexual life cycle, the offspring are genetically identical to the parent (they have exactly the same chromosomes)

  • In a sexual life cycle, the offspring are genetically distinct from each other and from each of the parents (their chromosomes are different, causing them to be genetically distinct)

• The halving of the chromosome number during meiosis is very important for a sexual life cycle as it allows for the fusion of gametes

• Sexual reproduction is a process involving the fusion of the nuclei of two gametes to form a zygote (fertilised egg cell) and the production of offspring that are genetically distinct from each other

• This fusion of gamete nuclei is known as fertilisation

  • Fertilisation doubles the number of chromosomes each time it occurs

  • This is why it is essential that the chromosome number is also halved at some stage in organisms with a sexual life cycle, otherwise the chromosome number would keep doubling every generation

  • This halving of the chromosome number occurs during meiosis

  • In animals, this halving occurs during the creation of gametes

Sexual lifecycle overview diagram

Sexual life cycle

Down Syndrome & Non-Disjunction

• Non-disjunction occurs when chromosomes fail to separate correctly during meiosis

• This can occur in either anaphase I or anaphase II, leading to gametes forming with an abnormal number of chromosomes

  • The gametes may end up with one extra copy of a particular chromosome or no copies of a particular chromosome

  • These gametes will have a different number of chromosomes compared to the normal haploid number

• If the abnormal gametes are fertilized, then a chromosome abnormality occurs as the diploid cell (zygote) will have the incorrect number of chromosomes

Diagram showing non-disjunction compared to normal chromosome separation

Image showing how chromosomes failing to separate properly during meiosis can result in gametes with the incorrect number of chromosomes

Down Syndrome

• A key example of a non-disjunction chromosome abnormality is Down syndrome, also called Trisomy 21

• Non-disjunction occurs during anaphase I (in this case) and the 21st pair of homologous chromosomes fail to separate

• Individuals with this syndrome have a total of 47 chromosomes in their cells as they have three copies of chromosome 21

• The impact of trisomy 21 can vary between individuals, but some common features of the syndrome are physical growth delays and reduced intellectual ability. Individuals can also suffer from issues with sight or hearing

• There are other examples of non-disjunction which result in trisomy

  • Patau syndrome (trisomy 13) and Edwards syndrome (trisomy 18) are very serious syndromes which result in many physical disabilities and developmental difficulties

• The risk of chromosomal abnormalities increases significantly with age

  • The age of the mother is particularly important in the case of Down Syndrome as non-disjunction is more likely to happen in older ova

• Karyotyping of the chromosomes in foetal cells can be used to identify chromosomal abnormalities

  • Foetal cells may be obtained by performing an amniocentesis or by chorionic villus sampling

Down syndrome karyotype diagram

A karyogram showing the karyotype of an individual with Down syndrome

Meiosis as Source of Variation

Crossing over and random orientation promote genetic variation

• Having genetically different offspring can be advantageous for natural selection and therefore increase the survival chances of a species

• Meiosis has several mechanisms that increase the genetic variation of gametes produced

• Both crossing over and random orientation result in different combinations of alleles in gametes

Crossing over

• At the start of meiosis, homologous chromosomes pair up with each other

  • As DNA replication has already occurred, each chromosome is made up of two sister chromatids

  • This means that a pair of homologous chromosomes is made up of four DNA molecules

• A pair of homologous chromosomes is known as a bivalent

  • Each pair consists of a maternal and paternal chromosome

• The pairing process resulting in the formation of a bivalent is known as synapsis

• After synapsis has occurred, a process known as crossing over may occur

• During crossing over, two non-sister chromatids (i.e. one chromatid from each of the homologous chromosomes) form a junction

• At this junction, the two chromatids break and rejoin with each other

• As these crossover events occur at exactly the same position on the two non-sister chromatids, this allows genes to exchange between the chromatids

• Non-sister chromatids are homologous but are not genetically identical and this means that some of the alleles of the exchanged genes will be different

• This process, therefore, produces chromatids with completely new combinations of alleles (that were not previously present in the DNA of the 'parent' cell)

  • This is because genetic material was exchanged between the maternal and paternal chromosomes

• As these chromatids will eventually be split up into different gametes, crossing over is of great importance because it is a significant source of genetic variation between gametes

  • This ensures there is genetic variation in populations of sexually-reproducing species, which is key to a species' ability to evolve and adapt to changes in its environment over time

Diagram showing crossing over

Crossing over of non-sister chromatids leading to the exchange of genetic material

Random orientation of bivalents

• At metaphase, during meiosis I, bivalents line up at the cell equator as they prepare to separate

• Spindle microtubules grow out from the poles of the cell and attach to the centromeres of the chromosomes

• Each of the two homologous chromosomes in a bivalent is attached to a different pole

• The orientation of the bivalents when they line up at the cell equator determines which pole each chromosome gets attached to (and eventually pulled towards)

• The orientation of the bivalents is completely random

• In addition, the bivalents also assort independently of one another (i.e. the orientation of one bivalent never affects the orientation of another)

Diagram showing random orientation

The orientation of bivalents lining up at the cell equator is random

The different combinations of chromosomes following meiosis

• The number of possible chromosomal combinations resulting from random assortment is equal to 2ⁿ

  • n is the number of homologous chromosome pairs or haploid number

• For humans: the number of chromosomes is 46 meaning the number of homologous chromosome pairs is 23 so the calculation would be:

  • 2²³ = 8,388,608 possible chromosomal combinations