Lecture 5: Extensions of Mendelian Genetics, Part 1 Flashcards
(44 cards)
issues with Mendel’s laws
- incomplete dominance and codominance
- multiple alleles
- pleiotropy
- variable expressivity
- incomplete penetrance
- environmental influence
how do we know that dominance is not always complete?
crosses between true-breeding strains can produce hybrids with phenotypes different from both parents
incomplete dominance
- F1 hybrids that differ from both parents express an intermediate phenotype
- neither allele is dominant nor recessive to the other
- the heterozygous phenotype is distinct from either homozygous phenotype (an intermediate phenotype)
- phenotypic ratios are the same as genotypic ratios
codominance
- F1 hybrids express the phenotype of both parents equally
- phenotypic ratios are same as genotypic ratios
- both alleles are expressed in the heterozygotes
draw a table portraying a summary of dominance relationships
give an example of incomplete dominance in plants
Antirrhinum majus (snapdragons)
P: red x white
F1 (all identical): pink x pink
F2: 1 red: 2 pink: 1 white
- the genotypic and phenotypic ratios are the same
- this signifies that the alleles of a single gene determine these 3 colours
give an example of incomplete dominance in animals
whippets:
- DNA testing has recently identified a mutation on the myostatin gene that tends to make whippets with one copy fast and whippets with two copies overmuscled ‘bullies’
give an example of incomplete dominance in humans
familial hypercholesteraemia
- results in abnormally high levels of cholesterol
- the general population (homozygous for fh) have <250mg/dl of plasma cholesterol
- heterozygotes for FH have 250-500
- homozygotes for FH have >500
can a gene have more than two alleles?
- genes may have multiple alleles that segregate in populations
- although there may be many alleles in a population, each individual carries only 2 of the alternatives
give an example of a gene that has more than two alleles
- ABO blood group gene: I
- 3 alleles: IA, IB, and i
- 6 possible ABO genotypes: IAIA, IBIB, IAIB, IAi, IBi, or ii
dominance relations are unique to
a pair of alleles; dominance or recessiveness is always relative to a second allele
dominance relations in the ABO blood group gene
- IA and IB are completely dominant to i but codominant to IB
how many possible phenotypes are there for blood type?
4: type A, type B, AB, or O
how is the ABO gene an example of codominant alleles?
the ABO gene encodes a cell surface protein, glycosyltransferase (an enzyme)
A allele: A antigen
B allele: B antigen
O allele: does not produce any antigens
- A and B antigens may be present on the same cell
- Alleles A and B are codominant
lentil coat pattern alleles are an example of
codominant alleles
describe the genetic mechanisms underlying lentil coat patterns
S allele: spotted
D allele: dotted
P: CSCS x CDCD
F1 (all identical): CSCD x CSCD (spotted/dotted)
F2: 1 CSCS (spotted): 2 CSCD (spotted/dotted): 1 CDCD (dotted)
draw a table of blood type and antibodies in serum
O is universal donor
draw a table of blood type of recipient vs compatibility with donor blood type
AB is universal recipient
how do we establish dominance relations between multiple alleles of a gene?
perform reciprocal crosses between pure-breeding lines of all phenotypes and observe the phenotype of the F1 heterozygote/hybrid
dominance series of agouti gene
A-: agouti
atat: black/yellow
aa: black
ata: black/yellow
A>at>a
pleiotropy
single gene determines more than one distinct and seemingly unrelated characteristics, controlling several functions and having many symptoms
some alleles may cause lethality. what does this mean?
type of pleiotropy where alleles produce a visible phenotype and affect viability: alleles that affect viability often produce deviations from a 1:2:1 genotypic and 3:1 phenotypic ratio predicted by Mendel’s laws
explain why lethality-causing alleles deviate from Mendelian ratios
- Mendel’s laws assume all genotypes are viable and equally fit.
- however, when an allele causes lethality, the affected genotypes drop out of the population, skewing the observed ratios.
King George 3rd’s ‘madness’
porphyria variegata
- caused by a mutation in the gene for the heme biosynthetic pathway, which encodes an enzyme
- if the enzyme is missing, porphyrin accumulates, resulting in concentrations that are high and toxic to organisms
- leads to multiple effects across urine (dark red urine), digestive system (abdominal pain and constipation), muscles (rapid pulse and weak limbs), and nervous tissue (stupor, delirium, convulsions, mad behaviour)