Types of mutations Flashcards
(16 cards)
Point Mutation
Occurs solely in the genome
A single base pair is deleted from, substituted or added to the sequence
Substitution (PM)
When a single nitrogenous base is substituted for another
Insertion (PM)
When a single nitrogenous base is inserted or added to the sequence
Deletion (PM)
When a single nitrogenous base is deleted entirely from the sequence
Silent mutations
Cause no change to the amino acid sequence
Only occur when more than one codon codes for a particular amino acid
Possible due to degenerate nature of DNA
Missense mutations
Result in an amino acid being replaced
Effect of this replace varies depending on position in protein
Whether the altered property can function
Nonsense mutation
Involve the insertion of the stop codon (TAA, TAG OR TGA)
Results in the transcription stage stopping prematurely
The protein is not completely formed
Chromosomal mutation
Move genes to other parts of a chromosome
Crossing over occurs in meiosis
Parts of one chromatid break off and become attached to another
Result in the rearranging of some genes
Duplication (CM)
Occurs when there are two copies of the same section on a chromosome
Insertion (CM)
Occurs when a segment of one chromosome breaks away
Break away is inserted into another
Deletion (CM)
Occurs when part of a chromosome breaks off and is lost
Inversion (CM)
Occurs when part of a chromosome breaks off and re-attaches in the opposite direction
This reverses the order of genes
Translocation (CM)
Occurs when a piece is moved from one chromosome to a non-homologous chromosome
Frameshift (PM)
Occurs when extra bases are added or deleted from DNA strand
Transcription of DNA is read in groups of three bases
Deletion or insertion of three, or a multiple of three, only affects one amino acid
More or less than three, the result can be more serious
The reading frame of the gene is affected
Nucleotide insertion (Frameshift)
Pushes the rest of the nucleotides back along the sequence
Nucleotide deletion (Frameshift)
Brings the rest of the nucleotides forward along the sequence