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
why is genetic diversity important?
if a population has a low genetic diversity, it might not be able to adapt to a change in the environment and the whole population can be wiped out by a single event (e.g. disease)
how can genetic diversity within a population be increased?
- mutations in DNA = new alleles (some can be advantageous whilst some can lead to problems)
- diff. alleles being introduced into a population when individuals from another population migrate into it and reproduce (this is called gene flow)
what are genetic bottlenecks?
- an event that causes a big reduction in the population (e.g. when a large no. of organisms die without reproducing)
- this reduces no. of diff. alleles in a gene pool
- meaning, reduction in genetic diversity
- the survivors reproduce, and a larger population is created from few individuals
describe the founder effect
- describes what happens when just a few organisms from a population start a new colony and there are a small no. of diff. alleles in the initial gene pool
- frequency of each allele in the new colony might be very diff. to the frequency of those alleles in the original population
- may lead to a higher incidence of genetic disease
- can occur as a result of migration leading to geographical separation or if a colony is separated from the original population for another reason (e.g. religion)
define natural selection
- when an allele codes for a specific characteristic which increases an organism’s chance of survival therefore, increasing the frequency of the population
- the fitter individual, who is better adapted to the environment, survives and passes on the advantageous alleles to future generations
how does natural selection work?
- there’s differential reproductive success in a population - individuals that have an allele that increases their chance of survival are more likely to survive, reproduce and pass on their genes (including the beneficial allele), than individuals with less advantageous alleles
- means a greater proportion of the next generation inherits the beneficial allele
- therefore, are more likely to survive, reproduce and pass on their genes
- so the frequency of the beneficial allele in the population increases from generation to generation
- over generations, this leads to evolution as the advantageous alleles have become more common in the population
define evolution
process where frequency of alleles in a gene pool changes over time due to natural selection
what are adaptations?
- features that help organisms to survive in their environment
- can be behavioural, physiological or anatomical
describe behavioural adaptations
- changes in behaviour which improve an organisms chance of survival
(e.g. playing dead)