7. Populations, Evolution & Ecosystems Flashcards
What is meant by the term genotype?
Genetic constitution of an organism
What is meant by the term phenotype?
The expression of this genetic constitution (genotype) and it’s interaction with the environment
What are alleles and how do they arise?
Variations of a particular gene (same locus) —> arise by mutation (changes in DNA based on sequence)
How many alleles of a gene can be found in diploid organisms?
2 as diploid organisms have 2 sets of chromosome (found in homologous pairs)
- but there may be many alleles of a single gene in a population
Describe the different types of alleles
Dominant allele - always expressed (shown in the phenotype)
Recessive allele - only expressed when 2 copies are present (homozygous recessive)/NOT expressed when dominant allele present (heterozygous)
Codominant alleles - both alleles expressed/contribute to phenotype (if inherited together)
What is meant by the terms homozygous and heterozygous?
Homozygous - alleles at a specific locus (on each homologous chromosome) are the same
Heterozygous - alleles at a specific locus (on each homologous chromosome) are different
What do monohybrid and dihybrid crosses show?
Monohybrid cross - inheritance of one phenotypic characteristic coded for by a single gene
Dihybrid cross - inheritance of 2 phenotypic characteristics coded for by 2 different genes
How do you represent the alleles for blood type, same gene with different alleles?
As a capital letter to the power of another capital letter
I^A, I^B, I^O
What is the dominance for alleles for blood group?
IA and IB are codominant
IO is recessive to IA and IB
How do you determine the probability that the next child will be a certain sex with a disorder?
Find the probability of the having the disorder and then multiply by 0.5
Explain the evidence from a pedigree diagram which would show that the allele for x disease is dominant
- diseased parents have a child without the disease
- so both parents must be heterozygous/carriers of the recessive allele
- if it were recessive, all offspring would have disease
Explain the evidence from a pedigree diagram which would show that the allele for disease x is recessive
- Parents without disease have a child with disease
- So both parents must be heterozygous/carriers of recessive allele
If 2 genes are on 2 different chromosomes and are not linked, what possible gamete combinations can occur?
e.g genotype AaBb
Gametes formed: AB, Ab, aB, ab
What is a sex-linked gene?
A gene with a locus on a sex-chromosome (normally X)
Explain why males are more likely to express a recessive X-linked allele
- Females (XX) have 2 alleles —> only express recessive allele if homozygous recessive/can be carriers
- Males (XY) have 1 allele (inherited from mother) —> recessive allele always expressed
Explain the evidence from a pedigree diagram which would show that the allele for Q disease on the X-chromosome is recessive
- Mother without Q has a child with Q
- So mother must be heterozygous/carrier of recessive allele
Explain the evidence from a pedigree diagram which would suggest that disease Q is caused by a gene on the X chromosome
Only males tend to have disease Q
Explain the evidence from a pedigree diagram which would show that the gene for disease Q is NOT on the X chromosome
- Q father has daughter WITHOUT Q
- Q father would pass on allele for Q in X chromosome of daughter, carrier of disease
- Q mother has son WITHOUT Q
- Q mother would pass on allele for Q on X chromosome so son would have disease Q
Explain how autosomal linkage affects inheritance of alleles
- 2 genes located on the same autosome (non-sex chromosome)
- So alleles on same chromosome inherited together
> stay together during independent segregation of homologous chromosomes during meiosis - But crossing over between homologous chromosomes can create new combinations of alleles
> if the genes are closer together on the autosome, they are less likely to be split by crossing over
In fruit flies, the genes for body colour and for wing development are not on the sex chromosomes. The allele for grey body colour, G, is dominant to the allele for black body colour, g. The alleles for long wings, L, is dominant to the alleles for short wings, l.
A cross was carried out between flies with grey bodies & long wings (heterozygous for both) and flies with black bodies & short wings.
The result of this cross was 225 offspring with a grey body & long wings and 220 with a black body & short wings. Explain these results
- the 2 genes are linked/autosomal linkage
- no crossing over occurs/genes are close together
- so only GL and gl gametes produced
What is epistasis?
Interaction of (products of) non-linked genes where one masks/suppresses the expression of the other
Describe when a chi-squared test can be used
- When determining if observed results are significantly different from expected results (frequencies)
> e.g comparing the goodness of fit of observed phenotypic ratios with exprected ratios - Data is categorical (can be divided into groups, e.g phenotypes)
What is an autosome?
A non-sex chromosome
Suggest why in genetic crosses, the observed phenotypic ratios obtained in the offspring are often not the same as the expected ratios
- Fertilisation of gametes is random
- Autosomal linkage/epistasis/sex-linkage
- Small sample size —> not representative of whole population
- Some genotypes may be lethal (cause death)