Diversity and Selection Flashcards
1
Q
Diploid Body Cells
A
- Normal body cells have the diploid number (2n) of chromosomes- meaning each cell contains 2 of each chromosome (a pair), one from mum and one from dad
- Chromosomes that make up each pair are the same size and have the same genes, although they could have different versions of the genes known as alleles (these pairs are called homologous pairs)
- Humans have 23 homologous pairs and so 46 chromosomes in total so diploid number for humans is 46
2
Q
Gametes in sexual reproduction
A
- Gametes are sperm cells in males and egg cells in females
- Gametes have a haploid number of chromosomes- they only contain one copy of each chromosome in a homologous pair
- Haploid number for humans is 23
- In sexual reproduction 2 gametes join together at fertilisation to form a zygote, which divides and develops into a new organism
3
Q
Fertilisation
A
- Haploid sperm fuses with a haploid egg, making a cell with the normal diploid number of chromosomes
- Half these chromosomes are from the father (sperm) and from the mother (egg)
- Any sperm can fertilise any egg- fertilisation is random
- Random fertilisation produces zygotes with different combination of chromosomes to both parents
- This mixing of genetic material in sexual reproduction increases genetic diversity within a species
4
Q
Meiosis definition
A
- Cell division that takes place in the reproductive organs of multicellular, eukaryotic organisms
- Cells that divide by meiosis are diploid to start with, but the cells that are formed from meiosis are haploid- chromosome number halves
- Meiosis in humans and mammals produce gametes directly
- In other organisms it produces haploid cells which later divide by mitosis to become gametes
- Without meiosis, you’d get double the number of chromosomes when the gametes fused which isn’t good
5
Q
Meiosis
A
- Before meiosis starts, the DNA unravels and replicates so there are two copies of each chromosome, called chromatids
- DNA condenses to form double-armed chromosomes, each made from 2 sister chromatids
- Sister chromatids are joined in the middle by a centromere
- Meiosis (first division)- chromosomes arrange themselves into homologous pairs
- Homologous pairs are then separated, halving the chromosome number
- Meiosis (second division)- pairs of sister chromatids that make up each chromosome are separated (centromere is divided)
- 4 haploid cells that are genetically different from each other are produced
6
Q
How to create genetic variation in gametes?
A
Crossing over of chromatids and independent segregation of chromosomes
7
Q
Crossing over of chromatids
A
- During meiosis I, homologous chromosomes come together and pair up
- Chromatids twist around each other and bits of chromatids swap over
- Chromatids still contain the same genes but now have a different combination of alleles
- Means that each of the 4 daughter cells formed from meiosis II contain chromatids with different alleles
8
Q
Independent segregation of chromosomes
A
- Each homologous pair of chromosomes in your cells is made up of one chromosome from your mum (maternal) and one from you dad (paternal)
- When homologous pairs are separated in meiosis I, it’s completely random which chromosome from each pair ends up in which daughter cell
- 4 daughter cells produced by meiosis have completely different combinations of those maternal and paternal chromosomes
- Shuffling of chromosomes leads to genetic variation in any potential offspring
9
Q
How many possible combinations in diploid species?
A
2n possible combinations of maternal and paternal chromosomes (n is number of homologous pairs) e.g. for humans there are 2^23 possible combinations
10
Q
What do Zygotes divide by in humans?
A
Mitosis
11
Q
Outcomes of mitosis and meiosis
A
- Mitosis= Produces cells with the same number of chromosomes as the parent cell, daughter cells are genetically identical to each other and to the parent cell, produces 2 daughter cells
- Meiosis= Produces cells with half the number of chromosomes as the parent cell, daughter cells are genetically different from one another and the parent cell, produces 4 daughter cells
12
Q
What is a gene mutation?
A
- Change in the DNA base sequence of chromosomes
- Order of DNA bases in a gene determines the order of amino acids in a particular protein so if a mutation occurs in a gene, the sequence of amino acids it codes for (and the protein formed) could be altered
13
Q
Substitution
A
One base is substituted with another
14
Q
Deletion
A
One base is deleted
15
Q
Effects of mutations
A
- Degenerate nature of the genetic code means that some amino acids are coded for by more than one DNA triplet
- This means that not all substitution mutations will result in a change to the amino acid sequence of the protein- some substitutions will still code for the same amino acid
- However, deletions will always lead to changes in the amino acid sequence beacuse it will change the number of bases present, which will cause a shift in all the base triplets after it