3.4.3 mutation and 3.4.4 natural selection Flashcards
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