Topic 4 - Diversity and Selection Flashcards
what is the diploid number?
- full number of chromosomes (2n)
- each cell contains 2 of each chromosome (a pair) - one from the mum and one from the dad
- diploid number in humans = 46 (23 homologous pairs)
what are gametes?
- sperm cells in males
- eggs in females
- have haploid number of chromosomes (only contain one copy of each chromosome in homologous pair)
- haploid no. in humans = 23
what happens to gametes in sexual reproduction?
- fuse together at fertilisation to form a zygote
- which, divides and develops into a new organisms
what happens during fertilisation?
- at fertilisation, a haploid sperm fuses with a haploid egg, making a cell with the normal diploid number of chromosomes
- half of these are from the father (the sperm), and half are from the mother (the egg)
- during sexual reproduction, any sperm can fertilise any egg - random
- random fertilisation produces zygotes with diff. combinations of chromosomes to both parents
- this mixing of genetical material in sexual reproduction increases genetic diversity within a species
describe meiosis
- type of cell division
- takes place in reproductive organs of multicellular, eukaryotic organisms
- original cell = diploid which then splits to form haploid
describe the process of meiosis
- before meiosis starts, DNA unravels and replicates so 2 copies of each chromosomes, called chromatids
- DNA condenses to form double armed chromosomes, each made from 2 sister chromatids. the sister chromatids are joined via the centromere
- meiosis I (first division) - chromosomes arrange themselves in homologous pairs
- these homologous pairs are then separated, halving the chromosome number
- meiosis II (second division) - the pairs of sister chromatids that make up each chromosome are separated (centromere is divided)
- four haploid cells that are genetically diff. from each other are produced
what are the 2 ways of creating genetic variation in gametes?
- crossing over of chromatids
- independent segregation of chromosomes
describe how crossing over of chromatids creates genetic variation in gametes
- 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 diff. combination of alleles
- the crossing over of chromosomes in meiosis I means that each of the 4 daughter cells formed from meiosis II contain chromatids with diff. alleles
describe how independent segregation of chromosomes creates genetic variation in gametes
- each homologous pair of chromosomes in your cells is made up of one chromosome from your mum (maternal) and one chromosome from your dad (paternal)
- when the homologous pairs are separated in meiosis I, it’s completely random which chromosome from each pair ends up in which daughter cell
- so 4 daughter cells produced by meiosis have completely diff. combinations of those maternal and paternal chromosomes - called independent segregation (separation) of chromosomes
- this shuffling of chromosomes leads to genetic variation in any potential offspring
what are the differences between mitosis and meiosis?
mitosis
- produces cells with the same no. 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 no. of chromosomes as the parent cell
- daughter cells are genetically diff. from one another and the parent cell
- produces 4 daughter cells
describe gene mutations
- involve a change in DNA base sequence of chromosomes
types of errors: - substitution - one base substituted with another
- deletion - one base is deleted
- the order of DNA bases in a gene determines the order of amino acids in a particular protein
- if a mutation occurs in a gene, the sequence of amino acids its codes for (and the protein formed) could be altered
what are some of the effects of mutations?
- degenerate nature of genetic code means some amino acids are coded for by >1 DNA triplet
- meaning, 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
- deletions definitely change the amino acid sequence as it changes the no. of bases present, causing a shift in all the base triplets after it (frame shift)
describe mutagenic agents and give examples
- things that cause an increase in the rate of mutations
- e.g. UV radiation, ionising radiation, some chemicals and some viruses
- increase the probability of a mutation occuring
describe chromosome mutations
- when meiosis goes wrong, and cells produced contain variations in the no. of whole chromosomes or parts of chromosomes = chromosome mutation and is caused by errors in meiosis
- chromosome mutations lead to inherited conditions because the errors are present in the gametes (hereditary cells)
- one type of chromosome mutation = chromosome non-disjunction (failure of the chromosomes to separate properly
e.g. Down’s syndrome
definition of genetic diversity
- number of diff. alleles in a species or population
- lots of alleles = large variety of diff. characteristics = high genetic diversity
- allows natural selection to occur because some alleles are more advantageous than others