Topic 4B - Diversity, Classification and Variation Flashcards
What are gametes?
They are the sperm cells and egg cells that join together at fertilisation to form a zygote, which divides and develops into a new organism
What is a ‘diploid cell’?
Cells that contain 2 of each chromosome, one from the mum and one from the dad (2n) e.g. normal body cells
What is a ‘haploid cell’?
A cell that only has one copy of each chromosome
What happens at fertilisation?
A haploid sperm fuses with a haploid egg to make a cell with the normal diploid number of chromosomes
- Half these chromosomes are from the father, and half from the mother
What is random fertilisation and why is it important?
It explains the way in which any sperm can fertilise any egg in sexual reproduction, to produce zygotes with different combinations of chromosomes to both parents
- Its important in introducing genetic variation within species
Where does meiosis take place?
In the reproductive organs
What does meiosis start with?
A diploid cell
What does meiosis produce?
4 haploid daughter cells
What are homologous pairs?
They are pairs of chromosomes that are the same size, have the same genes (only differing by alleles), and one chromosome in each pair comes from the mum and one from the dad
Describe the process of meiosis
DIAGRAM
- Before it starts, DNA unravels and replicates so there are 2 copies of each chromosome, called chromatids
- DNA condenses to form double-armed chromosomes, each made from 2 sister chromatids. Sister chromatids are joined in middle by centromere
- Meiosis I - Chromosomes arrange into homologous pairs
- Homologous pairs are separated, halving chromosome number
- Meiosis II - pairs of sister chromatids that make up each chromosome are separated (centromere divided)
- 4 genetically different haploid cells are produced
Why is meiosis needed?
- It is needed as without it, you’d get double the number of chromosomes when gametes fuse
- Introduces variation
What happens to chromatids during Meiosis I?
They twist around each over (in their homologous pairs) and bits of chromatids swap over
- The chromatids still contain the same genes but have a different combination of alleles
What are the 2 main events, during meiosis, that leads to genetic variation?
- Crossing over of chromatids
2. Independent segregation of chromosomes
How does the crossing over of chromatids’ lead to genetic variation?
It means that each of the 4 daughter cells contain chromatids with different alleles
- This leads to genetic variation
How does the ‘independent segregation of chromosomes’ lead to genetic variation?
- When homologous pairs are separated in Meiosis I, its completely random which chromosome ends up in which daughter cell
- So 4 daughter cells produced by meiosis have completely different combinations of those maternal and paternal chromosomes (Independent segregation)
- This ‘shuffling’ of chromosomes leads to genetic variation in any potential offspring
Give 5 differences between Mitosis and Meiosis
- Mitosis = produces cells with same number of chromosomes as parent cell /Meiosis = produces cells with half number of chromosomes as parent cell
- Mitosis = daughter cells are genetically identical to each other and parent cell /Meiosis = Opposite
- Mitosis = produces 2 daughter cells /Meiosis = produces 4
- Mitosis = 1 division /Meiosis = 2 divisions
- Mitosis = doesnt involve crossing over of chromatids or independent segregation, as theres no pairing/separating of homologous pairs/ Meiosis = does
What are chromosome mutations caused by?
They’re caused by errors during meiosis - sometimes, meiosis goes wrong and the cells produced contain variations in the numbers of whole chromosomes or parts of chromosomes
What can chromosome mutations lead to?
Chromosome mutations can lead to inherited conditions as the errors are present in the gametes (the hereditary cells)
Give an example of one type of chromosome mutation
Non-disjunction - a failure of the chromosomes to separate properly
What causes Down’s Syndrome
1- Down’s syndrome is caused by a person having an extra copy of chromosome 21 (or parts of it)
2- Non-dysjunction means chromosome 21 fails to separate properly during meiosis, so one cell gets an extra copy of 21 and another gets one
3 -When the gamete with the extra copy fuses to another gamete at fertilisation, the resulting zygote will have 3 copies of chromosome 21