3.4.3 mutation and 3.4.4 natural selection Flashcards
(38 cards)
allele
different version of the same gene
mutation
change in the base sequence of DNA
types of mutation
substiution, deletion, addition + insertion
silent mutation
as the genetic code is degenerate a change in the base sequence may still cause the correct amino acid to be coded for
why is deletion more likely to result in a mutation
deletion causes a frame shift in all triplets.
therfore all codons are affected
this changes all the amino acids coded for
why is substitution less likely to result in a mutation
only one base is affected, no frame shift
less severe effect on the polypeptide
mutagenic agents
agents that increase rate of mutation
chromosme mutation
changes in the structure or numbers of chromosomes
non-disjunction
failure of chromosome to seperate during meiosis
products of meiosis
4 genetically different haploid daughter cells
what occurs in meiosis 1
division of homologous chromosomes
what occurs in meiosis 2
division of sister chromatids
prophase 1
chromosomes condense + homologous chromosomes pair up.
centrioles move to opposite ends of the cell forming spindle fibres.
nucleolus disappears and nuclear envelope breaks down.
metaphase 1
chromosomes line up along the equator of the cell.
spindle fibres attach to the centromere of the chromosome
anaphase 1
homologous chromosomes are separated and pulled apart to opposite ends of the cell
telophase 1
chromosomes uncoil
nuclear envelop reforms around each set of chromosomes and nuclear envelope starts to reform
cytoplasm divides
prophase 2
chromosomes condense and are now visible
centrioles move to opposite ends of the cell forming spindle fibres
metaphase 2
chromosomes line up along the equator of the cell.
spindle fibres attach at the centromere of the chromosome
anaphase 2
centromeres pull apart each pair of the sister chromatids.
spindle fibres pull apart the chromatids to opposite ends of the cell
telophase 2
chromatids reach the opposite ends of the cell where they uncoil.
nucleolus and nuclear envelope reform.
cytoplasm divides
homologous chromosomes
one paternal and one maternal pair of chromosomes
how does meiosis lead to genetic variation
crossing over
independent segregation
crossing over
during prophase 1.
homologous chromosomes pair up.
the chromatids of each chromosome twist around each other forming a chiasmata.
forming new combinations of alleles.
independent segregation
during metaphase 1.
homologous chromosomes are randomly separated.
so which chromosomes ends up in each daughter cell is completely random.
therefore each daughter cell will have a different combination of daughter cells.