Biology topic 8 Flashcards
How can meiosis cause variation?
Crossing over- Homologous chromosomes align with each other, homologous portions of non-sister chromatids trade places
Independent assortment- During metaphase, random lining up of chromosome pairs
Sources of variation
Meiosis
Random fertilisation
Mutations
Gene (point) mutation
Miscopying of 1 or more nucleotides
Substitution, deletion, insertion
Changes protein made
Chromosomal mutation (translocation)
Changes position of genes within chromosomes
Chromosomal non-disjunction
Change in the number of chromosomes
An entire chromosome is lost or gained during meiosis
Mono-hybrid inheritance
Inheritance of a single gene
2 alleles for a single gene- 1 from male and 1 from female
Sex-linkage gene
Gene located on one of the sex chromosomes
(most located on the X chromosome)
Female gamete
XX
Homogametic
Male gamete
XY
Hereogametic
Men more likely to suffer from disorder because they only need 1 recessive allele for condition whereas women need 2
Haemophilia
Blood cannot clot properly
X linked recessive condition
Autosome
Non-sex chromosome
linked- genes on same chromosome
unlinked- genes on diff chromosomes
Gene locus (loci)
Specific location on a gene on a chromosome
Recombinants
New combinations of phenotypes that were not seen in the original parental phenotypes- shows crossing over has occurred
recombinant % = no. of recombinants/total x 100
The smaller the recombinant %, the closer they are on the chromosome, the less likely crossing over will occur
Genetic drift
Completely due to chance
Alleles are passed on
Bigger impact on smaller population
Population bottlenecks
Ecological event may reduce population sizes dramatically
Disasters are unselective- happen by chance
Small surviving populations are unlikely to be representative of original population
By chance alleles may be over-represented among survivors, some may be eliminated completely
Results in low genetic diversity