Utilisateur
A mutation is a change in DNA that affects genetic information.
Spontaneous mutations occur naturally at a low rate during normal cell cycles due to DNA breaks, incorrect DNA repair and replication errors
The base mutation rate is the speed at which spontaneous mutations occur in DNA
Mutagens are natural physical or chemical agents that increase the mutation eate by altering DNA structure or sequence
Chemical mutagens are substances that cause DNA mutations by altering bases or structure
Base analogues-substitube normal bases
nitrojs acid alters structrue and pairing
Radiation from the electromagnetic spectrum, especially ionizing radiation, damages DNA
Mutations cannot be passed to offspring but may cause diseases such as cancer.
Germline mutations are mutations in sex cells that can be passed onto offspring.
Genome mutations can affect a single base or large segments of chromosomes.
small scale mutations are mutations involving only one or a few nucleotides, such as Single and Multi nucleotides polymorphisms
large scale mutations are mutations that affect large DNA segmenrs
Mutations that affect a single gene
A point mutation is a mutation involving a single base change in DNA (SNP).
the types of point mutations single, missense, and nonsense mutations
They are mutations involving in the addition and removal or one or more nucleotides.
A frameshift mutation is a mutation that shifts the reading frame of a gene due to insertions or deletions.
An allele is a variant form of a gene.
Alleles are located at the same position, called a genetic locus, on a chromosome.
They are described as diploid organisms because they have pairs of each type of chromosome and therefore two alleles at each genetic locus in somatic cells.
One allele is inherited from each parent.
Because gametes are haploid, so they carry one allele per genetic locus.
Autosmal recessive inheritance refers to traits controlled by recessive alleles located on autosomes.
A carrier has one normal allele and one altered recessive allele but does not show the trait.
As the dominant normal allele produces enough functional protein.
As not all alleles show simple dominance, some are co-dominant or show incomplete dominance.
Co-dominance occurs when both alleles in a heterozygote are fully expressed
Some alleles are particularly dominant over others rather than completely dominant.
Black > brown
brown > light brown.
More than two alleles for a gene exist in the population.
Quantitative characters are traits that vary continuously within a population
Polygenic inheritance
Human skin colour
Epistasis is a genetic interaction where one gene alters how another gene is expressed.
One gene determines pigment colour, while another controls whether pigment is deposited in hair.
Because resources become limited as population size increases.
It provides differences that natural selection can act upon.
The process by which better-adapted individuals reproduce more successfully.
Random changes in allele frequencies, especially in small populations.
The formation of species overtime
Autosmal recessive inheritance.
Loss of function of an important protein.
A missense mutation in the ẞ-globin gene replacing glutamate with valine
They form a crescent shape and clump in red blood vessels
An autosmal recessive disorder caused bu deficiency of phenylalanine hydroxylase (PAH).
A defective chloride (salt) channel protein in cell membranes.
Thick mucus traps bacteria, causing chronic lung infections.
Carriers may have protection against severe diarrhoeal diseases like cholera.
An autosmal dominant, degenerative brain disorder.
Typically between 30-50 years
Males have only one X-chromsome.
The Y chromosome carries very few genes.
Through the maternal line only.
Diseases influenced by many genes and environmental factors.
They show continuous variation influenced by many genes
When one gene affects multiple traits.
