4.2 Meiosis Flashcards Preview

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Flashcards in 4.2 Meiosis Deck (19):

Define gamete

Haploid cells which fuse together during fertilisation to form a zygote (also called sex cells)


Describe a diploid cell

Contains 2 complete sets of chromosomes; chromosomes are in bivalents/tetrads. Body cells (somatic cells) are diploid.


Describe a haploid cell

Contains 1 complete set of chromosomes. Gametes (sex cells) are haploid.


Define tetrad

A pair of homologous chromosomes joined by a centromere (also called a bivalent)


Define meiosis

A reduction division of a diploid nucleus to form four haploid nuclei


Define homologous chromosomes

Homologous chromosomes are chromosomes that share: 
• The same structural features
• The same genes at the same loci positions (while genes are the same, alleles may be different)


Outline Prophase I of Meiosis I

1. Nuclear membrane breaks down, DNA in form of chromatin supercoils, condensing into chromosomes.
2. Homologous chromosomes undergo synapsis whereby they form Tetrads
3. 'Crossing over' occurs
4. The centrosomes move to the poles of the cell and spindle fibres begin to form and attach to the centromeres of the chromosomes.


Outline Metaphase I of Meiosis I

The homologous pairs are lined up horizontally along the equator by contraction of the spindle fibres.


Outline Anaphase I of Meiosis I

Continued contraction causes the homologs to separate and pulls the chromosomes to the opposite poles of the cell.


Outline Telophase I of Meiosis I

Nuclear membrane reforms, spindle fibres break down, chromosomes decondense back into chromatin. Cell divides into two haploid daughter cells (cytokinesis)


State the result of meiosis

4 haploid cells produced from 1 diploid cell


Define non-disjuncture

When a set of homologs in a tetrad do not separate during Anaphase I


Explain the cause of down-syndrome due to non-disjunction

• Caused by extra chromosome 21.
• Chromosomes or chromatids do not separate and go to the same pole.
• non-separation of homologous chromosomes during anaphase I due to incorrect spindle attachment.
• non-separation of chromatids during anaphase II due to centromeres not dividing.
• Occurs during oogenesis or spermatogenesis, but more common in egg formation.
• Egg or sperm contain an extra copy of chromosome 21, therefore zygote has 3 copies of chromosome 21.
• Thus Down syndrome is also known as trisomy 21.


Define karyotyping

When chromosomes are arranged in pairs according to their structure


Outline the process of karyotyping

• Pictures can be taken of the human chromosomes during the metaphase
• They can then be arranged into pairs on the basis of size and structure
• Chromosome 1 is the shortest, chromosome 22 is the longest
• The chromosomes appear as pairs of sister chromatids


Outline one use for karyotyping

• Amniotic fluid or chorionic tissue can be sampled as they contain foetal cells in mitosis.
• Can be used for diagnosis of chromosomal abnormalities, such as Down syndrome, identifying extra chromosome 21.


Define synapsis

The process by which tetrads are formed


Outline 'Crossing Over' of chromosomes in Prophase I

The homologous chromosomes in a tetrad cross over at a points called chiasmata. 'Crossing over' of genetic material between non-sister chromatids can occur at these points, resulting in new gene combinations (genetic variation).


Define chiasma

The point at which homologous chromosomes in a tetrad cross over