Lesson 8. Mutation
Lesson 8. Mutation
Lesson 8. Mutation
SCIENCE 10 - BIOLOGY
Bohari A. Saro
MUTATIONS
are changes or alterations in DNA
sequences. They usually manifest on
our physical characteristics.
HEREDITARY/GERMLINE MUTATIONS
these are inherited from parents
present in almost all the cells
ACQUIRED/SOMATIC MUTATIONS
occur because of lifestyle or
environmental factors like
exposure to chemicals or diseases
GENE
MUTATION
GENE MUTATION
an alteration in the sequence of
nucleotides in DNA
This change can affect a single
nucleotide pair or larger gene
segments of a chromosome.
TYPES OF GENE MUTATION
1. POINT MUTATION
2. FRAMESHIFT MUTATION
POINT MUTATION
change in a single nucleotide
types: deletions, insertions, or
substitutions of one nucleotide in a
gene
Silent:
a type of mutation where no
observable effect is observed on the
phenotype of the organism as the
result of the mutation
Missense:
a type of point mutation where the
substitution of a base pair results in a
different amino acid in the resulting
protein.
Nonsense:
is a type of point mutation where the
substitution of a base pair results in a
premature stop codon.
FRAMESHIFT MUTATION
where the nucleotides of a DNA
sequence are altered in a way that
changes one or more codons.
involving the insertion or deletion of
a nucleotide
CHROMOSOMAL
MUTATION
Karyotyping
process of pairing and arranging the
chromosomes based on its size to have a greater
idea about the organisms.
CHROMOSOMAL
MUTATION
affects a large portion of the DNA strand
can happen in both the autosomal and sex
chromosomes
can manifest in a range of physical and
developmental problems
TYPES OF CHROMOSOMAL MUTATION
1. Duplication
2. Inversion
3. Deletion
4. Translocation
Duplication
involves the production of one or
more copies of a gene or region of a
chromosome
is the inclusion of extra segments
of genetic material, such that a part
of a gene, all of a gene, or several
genes are redundant.
Duplication/Amplifications
Inversion
occur when a section of DNA breaks
away from a chromosome during the
reproductive process and then
reattaches to the chromosome in
reversed order
Inversion
Deletion
loss of genetic material. It can be small,
involving a single missing DNA base pair,
or large, involving a piece of a
chromosome.
mistake in the DNA replication process
which removes nucleotides from the
genome. A deletion mutation can remove a
single nucleotide, or entire sequences of
nucleotides.
Deletion
Translocation
chromosome mutations in which
chromosome segments, and the genes
they contain, change positions.
occur within a chromosome
(intrachromosomal) or between
chromosomes (interchromosomal).
Translocation
a detached part of a CHROMOSOME
becomes attached to another chromosome
or parts of two chromosomes may be
joined
may be inherited or acquired. In many
cases they cause no effect on the body
because all the normal chromosomal
material is present.
Translocation
Aneuploidy
is a type of mutation that changes parts of
a chromosome set, resulting in either the
loss of one or more chromosomes or the
addition of chromosomes.
Aneuploidy
Applications
The mutations can be used as a method of designing
special arrangements of genes uniquely to solve
different biological issues.
Chromosomal mutations are also essential at the
applied level in medicine, plant, and animal breeding.
These mutations play an important role in the
evolutionary process by shaping the genomes and
chromosomes of different organisms.
Thank you