GENETIC DIVERSITY Flashcards
whats a gene muatation
-change in the base sequence of DNA on chromosome
-can arise spontaneously during DNA replication (interphase)
-involves base deletion/substitution
changes to one or more bases in DNA triplet could result what
change in amino acid sequence of the polypeptide
Why might a mutation not lead to a change in the amino acid sequence
-Genetic code is degenerate, so may code for the same amino acid
-may change an intron which is not expressed
When does gene mutation by deletion of bases occur
when a nucleotide is lost from the normal DNA sequence
what does 1 deleted nucleotide cause
-causes all triplets in a sequence to be read differently
-because each has been shifted to the left by one base
two forms chromosome mutation can take
-changes in whole set of chromosome
and
- changes in the number of individual chromosomes
describe changes in whole set of chromosomes
-occurs when organisms have 3 or more sets of chromosomes rather than usual 2
-called polyploidy + occurs mostly in plants
describe changes in the number of individual chromosomes
-sometimes individual homologous pairs of chromosomes fail to separate during meiosis (non-disjunction)
-usually results in gamete having either 1 more or 1 fewer chromosome
-eg down syndrome
What is a mutagenic agent?
a factor that increases the risk of mutations
What is a frame shift mutation?
-the mutation results in the rest of the base sequence being impacted,
-therefore causing a greater impact of the codons
-therefore the amino acid sequence that is coded for.
mutation can lead to production of non-functional protein/enzyme
-changes in base/ triplet sequence of DNA
-changes sequence of codons on mRNA
-changes sequence of a.a in primary structure of polypeptide
-changes position of H/ ionic /S-S bonds in tertiary structure of protein
-changes tertiary structure and thus shape of protein (and active site if enzyme)
-(if enzyme substrate can’t bind to active site and form enzyme substrate complex)
Base deletion process
-one nucleotide / base removed from DNA sequence
-changes triplet/codon from point of mutation (frameshift)
-changes sequence of codons on mRNA after point of mutation
-changes sequence of a.a in primary structure of polypeptide
-changes position of H/ionic/S-S bonds in tertiary structure of protein
-changes tertiary structure, thus shape of protein
Base substitution process
-nucleotide /base in DNA replaced with another nucleotide/base
-change in one base = changes one triplet
-changes one mRNA codon and one a.a > sequence of a.a in primary structure of polypeptide changes etc
-OR due to degenerate nature of genetic code , the new triplet may still code for same a.a so sequence of a.a in primary structure of polypeptide remains unchanged
products of meiosis
-4 daughter cells
-each with half the number of chromosomes as the parent cell
Process of meiosis
-before meiosis starts. DNA replicates so there’s 2 copies of each chromosome (sister chromatids joined by centromere)
-homologous pairs line up randomly and one from each pair move either side of the cell
-independent segregation (increases genetic variation in gametes)
-crossing over - recombination occurs where chromosomes swap genetic material
-homologous chromosomes separate
-4 new daughter cells are formed