1.6 Flashcards
What is a mutation?
Mutations are a change in the structure or amount of an organisms DNA. Mutations arise spontaneously and at random
Frequency of mutations
Mutations are rare. In humans it is estimated that there is 1 mutation per 15-30 million base pairs. Mutation rates differ in different genes and different organisms
Types of mutations
- Single gene mutations
- Chromosome structure mutations
- Polyploidy
Single gene mutations
These mutations involve a change in one of the base pairs in the DNA sequence of a single gene. Also known as point mutations. These may occur in the protein-coding sequence or the regulatory sequences which control expression of the gene.
There are 3 types of point mutations (gene mutation):
- Deletion
- Insertion
- Substitution
Problems caused by substitution: Sickle cell anaemia
Genetically transmitted disease
Caused by abnormal hemoglobin (protein)
Known as a point mutation (substitution)
Problems caused by insertion and deletion
- Brings about a major change in the protein which is made since a large section of DNA is affected
- Many amino acids are altered which results in a non-functional protein (known as a lethal gene)
- This is known as a frame shift mutation
- Sometimes a metabolic pathway enzyme is affected and the pathways is disrupted e.g. Phenylketonuria
Phenylketonuria
- Gene mutation results enzyme not produced that changes phenylalanine to tyrosine
- Phenylalanine concentration builds up within body of the newborn baby
- Phenylalanine is converted into toxic substances
- The toxic substances cause irreversible damage to the developing brain
RNA splicing is important in __________. Mutations in the area that marks the start or end of an intros, may lead to one or more _______ not being removed. This will lead to a creation of a protein that _______ function properly
Creating the mature mRNA transcript before it is translated into a protein
Introns
Doesn’t
Thalassemia
Thalassemia is a type of anaemia (similar to Sickle Cell) where a police site mutation has caused a defect in the synthesis of hemoglobin. Thalassemia, a disease caused by a defect in hemoglobin synthesis, is caused by a splice site mutation
Types of chromosome structure mutation
- Duplication
- Inversion
- Translocation
- Deletion
Duplication
- duplicated genes may undergo mutation
- this can introduce a new characteristic that may or may not be advantageous
- duplication of a gene produces a second copy of the gene which is free from selection pressure (it can become altered without affecting the original genes function)
Inversion
- reversal of sequence
- problems with pairing and crossing over in meiosis
- often non-viable gametes
Deletion
- drastic effect
- humans: cri du chat (mental retardation)
Translocation
- sections attaching to non-homologous partners
- problems win pairing in meiosis
- translocation involves transfer of genes from one chromosome to another
- this results in problems pairing chromosomes during gamete formation and leads to non-viable gametes