chapter 9 - genetic diversity Flashcards
What is a gene mutation ?
- a change in the DNA base sequence
How do mutations occur and what are thing that increase the rate of mutations ?
- they occur spontaneously if dna is misread during dna replication
- things that increase the rate of mutations are mutagens
- like ultraviolet/ionsing radiation, chemicals and viruses
What are the three types of mutation ?
- substitution
- deletion
- insertion
How do mutations affect the protein synthesis ?
- they can leas to a different amino acid sequence
- as the gene has changed
- this means we will get a different polypeptide
- and probably a different tertiary structure
What are substitution mutations ?
- when one base is replaced by another
- which can cause the amino acid sequence to change
- but not all substitutions change the amino acid sequence
- because there is more than one triplet code that codes for the same amino acid
- this is the degenerate nature of dna
What are deletion mutations ?
- when one base is removed from the sequence
- if a base is deleted, the base sequence shifts
- so all the triplets after the deletion change so the amino acid sequence also changes
- this is a frame shift
What is an insertion mutation ?
- when one base is added to the sequence
- this also causes a frame shift
- and all the triplets codes after the insertion change so the amino acid sequence will also change
What are missense, nonsense and frame shift mutations ?
- missence is when an amino acid is replace by another one because of a change to the triplet code
- nonsense is when there is a premature stop codon weaning not all the amino acids join the chain
- frame shift is when a base is added or removed so codons shift to either side so all the codons are read different so the amino acid is different
What is chromosome mutation ?
- when there is a change to the structure or whole number of chromosomes
- these can happen spontaneously through cell division
What are the two types of chromosome mutation ?
- polyploidy = when organisms have more than two sets of chromosomes, mostly seen in plants
- non-disjunction = when homologous chromosomes don’t separate during meiosis meaning there are gametes with extra or missing chromosomes , which leads to individuals with missing or extra chromosomes in all cells
What is meiosis ?
- a type of cell division where a parent cell divides into 4 haploid cells where they are all genetically different from each other
- it involves 2 nuclear divisions
What area the 2 stages of meiosis ?
- meiosis 1 - homologous chromosomes are separated
- meiosis 2 - chromatids are separated
-before this interphases happens so that each chromosome has 2 chromatids ( so each homologous chromosome has 2 chromatids )
What are the 2 stages of meiosis that introduce variation ?
- independent segregation of homologous chromosomes
- crossing over between homologous chromosomes
- the both happen in meiosis 1
Wha is crossing over ?
- during prophase 1, when the homologous pairs line up on either side of the equator , the form a bivalent
- and the chromatids ( from each chromosomes ) can become twisted around each other
- the crossing over is called a chiasma
- tension can then cause these chromatids to break off and attach to the other chromatid ( from the other homologous chromosome ) .
- this results in new combinations of alleles on each of the homologous chromosomes
What is independent segregation ?
- when the homologous chromosmes line up on either side of the equator
- aka 23 pairs have lined up
- it’s random which side the paternal or maternal chromosome might line up on
- e.g all paternal chromosomes might be on one side
- there are 2^23 ways that the chromosomes could organise themselves
- formula for this is 2^n ( n = umber of homologous pairs )
What happens in prophase 1 ?
- the chromosomes condense and homologous pairs line up
- centrioles migrtae to opposite sides of the cell and they each start to form spindle fibres
- the nucleolus disappears and the nuclear envelope breaks down which leaves the chromosomes free in the cytoplasm
What happens in metaphase 1 ?
- homologous pairs line up at the equator of the cell
- each chromosome’s centromere attaches to the spindle
What happens in anaphase 1 ?
- homologous chromosome pairs are separated an pulled to opposite poles of the cell
- but the chromatids are still joined together
What happens in telophase 1 ?
- chromosomes reach opposites sides of the oil where they uncoil
- nuclear envelope forms around each set of chromosomes and the nucleolus starts to reform
- cytoplasm divides to form 2 cells
What happens in prophase 2 ?
- chromosmes condense again
- centrioles migrate to opposite sides of the cell , each centrioles begins to form spindle fibres
- nucleolus disappears again and the nuclear envelope breaks down
What happens in metaphase 2 ?
- chromosmes line up in the equator of the cell ( so 23 chromosomes line up )
- each chromosomes’s centromere attaches to a spindle
What happens in anaphase 2 ?
- centromeres from each chromosomes divide and separate it to a pair of chromatids
- spindle fibres contract and shorten so chromatids are pulled to opposite sides of the cell
What happens in telophase 2 ?
- chromatids reach the opposites sides poles of the cell whee they uncoil and become long and thin again
- nuclear envelope forms around each set of chromosomes and they form 2 nuclei and the nucleolus starts to reform
- cytoplasm divides and 4 cells are produced
What is genetic diversity ?
- the number of different alleles of genes in a population
- this is what lets natural selection happen