How species evolve 11 Flashcards
Point mutation
- a mutation that alters one nucleotide
- example: silent, missense, and nonsense mutation. ( addition or deletion; frameshift)
- ( singular nucleotide frameshift muatation can be considered as point mutation but not double nucleotide)
Nonsense mutation
- a mutation in when a nucleotide is substituted
for another, changing the codon to
a stop codon, ceasing transcription
on the gene. - Thus, gene will not be completely transcribed, resulting in a polypeptide that is too short to function
- most dangerous sub mutation as it permantly ends transcription genes
Silent mutation
- a mutation when a nucleotide is substituted for another, changing the codon, while coding for the same amino
acid. - Thus, there is no effect on protein structure, because redundancy
Missense mutation
- a mutation in when a nucleotide is substituted
for another, changing the codon that codes for a differnt amino acid. - thus, this alters the primary structure of the polypeptide –> affects function of protein
Frameshift mutation
- a mutation that involves the insertion or
deletion of one or two nucleotides, - affecting every codon from thatpoint forward as the reading frame is altered( as it is shifted )
- Thus, major disruptions to structure and function
- e.g. can be base insertion/ deletion mutation
Reading Frame
the order in which nucleotide triplets or codons are
read to match complementary base
base insertion mutation FS
a nucleotide is added to a gene,
affecting every codon from that
point forward
base deletion mutation
a nucleotide is removed from a gene,
affecting every codon from that
point forward
Block mutations
-affects a large chunk of DNA, or an entire geneby altering the structure of a chromosome by deletion, duplication, inversion, and translocation of clusters of nucleotides
Block mutation: deletion mutation
- a section of DNA is removed from a chromosome, shortening the DNA.
Block mutation: duplication mutation
- a section of DNA is replicated, lengthening the DNA
Block mutation: inversion mutation
- a section of DNA has its sequence reversed.
Block mutation: translocation mutation
-when two sections of DNA on different chromosomes
switch places.
aneuploidy
- when a cell or organism varies in the usual number of chromosomes in its genome by the addition or loss of
a chromosome - seen in individual’s karyotype and during stem from issues during meiosis
Polyploidy
- when an organism contains additional sets of each
chromosome in its genome. - addition set of chromosome in embryos are fatal and thus, invidials can’t survive as halpoid ( N).
- common in other organisms such as plants as an advantage is it increases size and hardness in fruit but they are unale to reproduce sexually
What do mutation do to genetic diversity?
- mutation introduces new alleles into a population and this increases genetic diversity
- mutation can be beneifical, neutral or delterious
Mutagen
agents that can cause
mutations in DNA
- e.g. UVradiation–> skin cancer
Deleterious
alleles that have an
overall negative effect on individual
fitness when expressed
Alleles
variants of a gene
Allele frequency
the proportion of
certain alleles in a gene pool
gene pool
all the genes in
a population
Germline cell
cells involved in the
generation of gametes
in eukaryotes( reproductive system)
phenotype
the physical or biochemical characteristics of an organism, resulting from expression of a gene (or set of genes) and interaction with the environment
somatic cell
any cell in an
organism that is not a germline cell, body cells and when mutations occur it cannot be inherited
List examples of aneuploidy conditions
- Down syndrome
- Edwards syndrome
- Klinefelter syndrome
- Turner syndrome
Mutation and common symptoms of Down syndrome
- Trisomy 21
-Decreased muscle tone, short neck, flattened
facial profile and upward slanting eyes
Mutation and common symptoms of Edwards syndrome
- Trisomy 18
-Very small weight, small head, long and
underdeveloped fingers
Mutation and common symptoms of Klinefelter syndrome
- XXY
- Typically tall, infertile, enlarged breast tissue. Only
affects phenotypic males
Mutation and common symptoms of Turner syndrome
- X0
- Typically infertile, short height and fused neck and
head. Only affects phenotypic females
Steps of Natural selection
- Many physical, biochemical or behavioral variation in phenotypes between individuals in a population
- variation is heritable
- Specific selection pressure causes a struggle for survival.
- individuals with advantageous phenotype survive and reproduce
- Pass their alleles onto the next generation.
- This changes the allele frequencies in the population as the trait becomes more common
Steps of Natural selection: 1. Variation
- Individuals in a population vary genetically. This leads to phenotypic differences.
e. g.
- One species of moth has two genetic
variants: black and white.
Steps of Natural selection: 2. Heritability
- These traits - whether advantageous
or disadvantageous for survival and reproduction - alleles can be passed on from parents to offspring
e.g.
- Body colour is heritable - parents with white body colour are likely to have whit body offspring , while parents with black
body colour are likely to have black body offspring.