Task 3 Flashcards
artifical insemination
nature
manual injection of male sperm into female reproductive tract
used for cattle
used to produce offpsring with favourable characteristics
artifical insemination
adv
minimises cost of transporting animals together
sperm cell can be frozen and transported
more offpring produced than regular breeding
can inseminite many females
Artifical insemination
disadv
using method at mass reduces genetic varation
can inseminate many females –> male alleles become more dominant in pop
higher ratio of alleles selected by breeders rather than by nature
Artifical pollination
nature
manual transfer of pollen dusted upon the stigma of another plant
Artificial pollination
Adv
Cost effective
Increases genetic diversity through hybrid species –> new
combinations of alleles
Improvs cross breeding
Artifical pollinaion
Disadv
Overuse leads to reduces genetic diversity
Passing on a limited array of genes/allele combinations –> propogate unhelpful diseases
Cloning general
Asexual reproduction
Used to create offpsirng gentically identical to parent
Plant cloning and animal cloning
Cloning adv
Plants and animals with favourable characteristics
Cloning disadv
Lack of genetic diversity –> susceptible to an entire wipeout by disease or selective pressure
In vitro fertilisation general
where an egg is fertilised by a sperm outside the mother’s body
in petri dish
resulting zygote is cultured until early stages of development
transferred into surrogate mother uturus
IVF adv
Advantegous alleles which would not naturally have been passed on can be inhereited by offpsring
IVF disadv
genetic diversty of population reduced
genes for infertility passed on
sperm banks ca alter genetic composition of population (only desirable traits of sperms listed)
Cloning for plants
Cutting or grafting a plant
E.g. tissue culture
cutting piece of stem/ root/leaf and culturing in a nutrient medium
Animal cloning
Dolly the sheep (1990s)
Removing the nucleus from an unfertilised egg and putting nucleus of other animal (donor)
implanting egg into surrogate mother
The use of scientific knowledge leads to:
(effect on agriculture manipulation)
- asexual techniques eg cloning plants through plant propagation, –> allows the rapid development of plants with known qualities.
- the artificial selection of favourable characteristics in plants, greater diveristy in foods, plants?
- reproductive technologies –> manipulate animal reproduction eg artificial insemination, IVF, whole organism cloning such as Dolly the sheep.
- gene technology or genetic engineering, which results in genetically modified organisms.
Varation occurs through
(meiosis processes)
- Mutations
- Crossing Over (during Prophase I)
- Independnant assortment (during Metaphase I)
- Process of fertilisation
Crossing over
when does it happen
the possible exchange of alleles at the chiasma of homologous chromosomes
Prophase I
Independent assortment
when
the division of homologous chromosomes to seperate poles
Metaphase I
chromosomal mutations
large scale mutations that affect the overall structure of a chromosome or the entire number of chromosomes in a cell are altered.
genes
a segment of DNA on a chromosome that determines inherited characteristics
alleles
alternative forms of the same gene
example of autosomal dominant disease
huntington’s disease
does not skip a generation
exmaple of autosomal recessive disease
cystic fibrosis
examples of sex linked diseases
haemophilia (X linked, females are carriers or affected, all male affected)
colour blindness
Purpose of allele frequency data
Understand variation
Predict potential of population to adapt, resilience and survival of species
Gene pool
sum total of all the genes and their alleles within a population
Genetic diversity
the total of all the genetic characteristics in the genetic makeup of a species
population genetics
the study of how the gene pool of a population changes over time and space
single nucleotide polymorphism
SNPs
Base substitution mutations (alleles) that commonly occur within the species population (in 1% of species)
Uses of single nucelotide polymorphism
genetic marker to determine the population’s susceptibility to a certain disease e.g. asthma, Alziemer’s
help predict an individual’s response to certain drugs,
SNPs at higher frequences used to indicate presence of particular disease
Adv of single nucleotide polymorphism
identify cause and effect relatipnship between SNP and disease
Cheapter than sequencing genome
DNA sequecning
the process of determining the precise order of nucleotides within a segment of DNA
Methods of DNA sequencing
Sanger chain termination method
DNA sequencer
Sanger chain termination gerneral
Replicating DNA strands outside of cells with ddNATP attachments that stop the chain from growing/adding upon
Sanger chain termination steps
- Isolate DNA from the cells of the organism
- Sequence reactions
- Fragment of DNA produced are then sorted by length using capillary electrophoresis
- Results are analysed by a computer
Factors affecting genetic variation in a gene pool
size of population, mutation, natural selection, genetic drift, diversity of the environment, migration pattern
DNA profiling
identify and compare indivduls by characteristics in their DNA
using regions of DNA containing STRs
STRs
short sequences of DNA, usually 2-5 base pairs long that repeat numerous times
Uses of DNA profiling
Forensics: or crime scenes with fingerprints, although too few loci makes false positives
Paternity studies: can compare possible fathers to confirm or refute paternity using bands of mother and father
Pedigree determination in animals: ensure breeder has gained correct parents for animal breeding using DNA fingerprints
uses of population genetics data
conservation genetics (cheetah, pymgy possum)
inheritance of diseases (breast cancer)
mutations
permanent change to the DNA sequence of an organism
importance of mutations
new variation/alleles increases the chance of a population’s survival during environmental change.
Without mutations, natural selection cannot occur.
Mutagens
electromagnetic radiation sources
Ionising radiation: breaks chemical bonds causing damage to DNA, many fractures can overwhelm enzymes to cause mistakes in DNA
UV Rays: promote a chemical reaction of bases fusing together e.g. two thymine bases, cause bulge in DNA and disrupt normal transcription and replication
Mutagens
chemicals
Intercalating agents: insert into DNA base sequence, causes stretch and DNA polymerase to insert extra base –> frameshift mutation occurs
Base analogous: chemicals with physical structure to nitrogenous bases when incorporated in DNA
Reacting Chemicals: react with the nitrogenous bases and chemically modify the DNA
Example: Carcinogen in cigarrettes
Types of mutagens
ionising electomagnetic radiation
chemicals
biological mutagens/naturally occuring
Mutagens
naturally occuring/biological
Biological Mutagens: release of free radicals. from metabolism processes, cause oxidation of DNA, breaking DNA strands
Viruses: insert genetic information into chromosomes of host cell, causing disruption to normal cell function e.g. HPV –> oncogenic (cancer causing) virus that causes cervical cancers.
Example of point mutation
Sickle cell anemia
Mutations
Effect on proteins
Nonsense: changing an amino acid to a stop codon, cutting the protein short. This resulting protein is normally non-functional
Misense: a point mutation that results in 1 amino acid change
e.g. E.g. sickle cell anaemia: CTC changes to CAC, altering amino acuds and shape of haemoglobin
Silent: no change caused in amino acids. (swapped base in the triplet, still coding for the same amino acid)
Frameshift: an insertion or deletion
–> shifts entire reading frame of RNA, creation of a whole sequence of incorrect amino acids and production of a non-functional protein.
Chromosomal mutations
Inversion
Translocation
Inversion: a section of DNA is removed, turned 180 and then reinserted into the chromosome so that the bases are in reverse order.
Translocation: a section of DNA is moved from one chromosome to another.
Aneuploidy
An extra or missing chromosome
Caused by nondisjunction: failure of homologous chromosomes to separate during cell division
e.g trisomy
Causes of mutations
Spontaneous
Induced (mutagens)
Polyploidy
more than two haploid sets of chromosomes, e.g. triploidy
Effect of somatic mutation
may lead to a localised effect, such as the development of a tumour in a part of the organism, but it will not be passed on to the next generation.
or lead to cell dying, or no effect
Effect of germline mutation
becomes incorporated within DNA of every cell within the offspring’s body
Exmaple of somatic mutation
skin cancer
Example of germline mutation
haemophilia
Segments of coding dna
exons (gene)
Segments of non-coding dna
enhancers/silencers/regulators
promoters
introns (gene)
Exons function
Codes for proteins that carry out biological functions.
Introns function
Code for their own removal during mRNA splicing (end of transcription)
Promoter function
Tell the enzyme RNA polymerase where to bind RNA to DNA which begins the transcription.
Significance of mutation in
Exons
Can directly impact the sequence of amino acids and therefore affect the functioning of proteins.
Changed DNA code = changed mRNA = mutated protein
Significance of mutation in
introns
Have the potential to affect splicing of DNA (mutation in introns causes removal of exons = deletion).
Significance of mutation in
promoter
Mutation can result in polypeptide chains not being fully transcribed, causing deficient proteins