genetic diversity Flashcards
why genetic code in degenerate
most amino acids coded for by more than 1 triplet
non overlapping
each base is only needed once
universal
each triplet codes for the same amino in all organisms on earth
transciption makes
mrna
translation makes
polypeptide
primary strcutre
the sequence of amino acids
tertiary structure
3d strucutre determines by hyrodgen ionic and disulphide bonds
mutations
a change in the dna base sequence or quantity
causes of mutation
-spontaneous during dna replication
-due to mutagens which acceleates the rate of spontaneous mutations
-eg.high energu/ioinising radiation , some chemicals
-increases genetic diveristy which is important in natural selection and speciation
types of gene mutation
substitiution
addition
deletion
duplication
inversion
transloaction
substiituion
addition
duplication
deletion
one base replaced by another
extra base added to sewuence
a base repeated
base is deleted
nonsense
a stop codon -shortened polypeptide
mis sence
a diff amino aicd - affects fiuncitoning of polypeptide
silent
same amino acid
insertion mutation
a mutation that occurs when a nucleotide with a new base is randomly inserted into the dna sequence
what does insertion mutation change
changes the amino acid that wouldhave been coded for by the original base triplet as it creates a new different triplet of bases this is because every group of three bases in a dna sequence codes for an amino acid
what is a frameshift mutation
changes the triplets further on in the dna sequence
this may dramatically change the amino acid sequence produced from this gene and therefore the ability of the polypeptide to function
haploid cells
have a single copy of each chromosomes
homologous pair
pair of chromosomes
one maternal and one paternal - same gene loci
diploid
nucleus has 2 sets of chromosomes
gametes formation
human cells 46 chromosomes
diploid 2n=46
gametes-23 chromseomes one of each homologus pair and 1 sex chromoskmes
haploid = n=23
independent assortmrnt
one chromodome
2 vhromatids from each homologus pair ends up in each gamete
each homologus pair lines up independent of any others
this depends on their random alignment during meiosis
crossing over
homologus region of line up chromatids may be exchanged by bresking and rejoining at regiond vslled chiasma
joining with another set of chromosomes at fertillisation ensures variation