dna replication meiosis Flashcards
homologous pair
one pair from each parent; same gene but different alleles
gamete
haploid sex cell
haploid
(n)
a cell with a single set of unpaired chromosomes
(one of each homologous pair)
diploid
(2n)
a cell with two complete sets of chromosomes
(both homologous pairs)
fertilisation
fusion of 2 haploid cells to form a zygote
what happens before meiosis
dna replication where diploid doubles its chromatids
which forms sister chromatids joined by a centromere before starting prophase I
(doesn’t change actual chromosome no.)
difference between meiosis and mitosis
meiosis:
cell division to form haploid (gametes)
2 divisons => 4 daughter cells
genetically different
mitosis:
cell division for growth of organism and repair of tissues
1 division => 2 daughter cells
genteically identical
what happens during meiosis
homologous chromosomes pair up
crossing over
produces new combo of alleles
chromosones sepearate at random
produces varying combos of genes
chromoarids separated at meiosis II
two ways in genetic variation is introduced
Crossing over: Different combination of alleles
During metaphase I, where chromatids of homologous pairs cross over and swap alleles
(produces chiasmata: crossed over holograms pairs)
Independent segregation: different combination of chromosomes
gene mutation
random change to the base sequence of DNA during DNA replication
Substitution
swapping one base for a different base
deletion
one or more bases is remove which causes a frame shift and changes the following triplets
how do mutations cause a non-functional protein?
Change to DNA triplet during replication
Change to mRNA codon
Different anticodon => different amino acid, which changes primary structure of protein
Hydrogen, ionic and sulphate binds made in different places
Changes tertiary structure
change in active site so no e-s complexes form
why no change to sturcture of protein
DNA is degenerate
Each amino acid is coded for y more than one triplet codon
Change to DNA base (substitution) might not cause a change to amino acid in primary structure
No changes to bonding, therefore also not to tertiary structure
chromosome non-disjunction
when chromosomes don’t separate properly during meiosis I or meiosis II
This causes an uneven no. of chromosomes in the gametes
Genetic disease eg. Down’s syndrome