Genetics [a d]
Transcript of Genetics [a d]
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is the study of heredity
is the process in which traits are passed from parents to offspring
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Historical ViewGregor Mendel: 1866 – first publicationOscar Hertwig: 1876 – discovered meiosisThomas Morgan: 1910 – sex-linkage in
Drosophila Murray Llewellyn Barr: 1948 – Barr bodyMary Lyon: 1960 – inactivation of X
chromosome in calico cats
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Gregor Mendel
(1822-1884)
Austrian monk who formulated fundamental laws of heredity in early 1860s
Experimented with peas
Over seven years, he made crosses with 24,034 plants
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Mendel used sweet peas for his experiments. WHY? Cheap Easy to grow Could pick traits that
were easy to follow Rapid generation time Lots of offspring Can self-fertilise or be
cross-fertilised
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Traits (observable characteristic) studied by Mendel:
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A controlled cross between two parents
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Mendel’s Crosses:Pollen from one parent was
transferred to the stigma of the other parent. Parental generation = P
Resulting offspring = first filial generation or F1
Mendel’s workplace
If F1 plants self pollinate, produce second filial generation or F2
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Basic points revised:Diploid (2n) : total number of
chromosomes2n = 4
n = 2
The human diploid number is 46 44 autosomes 2 sex chromosomes
But chromosomes are pairedThe unpaired chromosome complement is
called haploid (n)
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How many are autosomes out of the 23 chromosomes? 22
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• have the same length and carry the same gene sequences
• alleles: alternative forms of a gene reside at the same locus on homologous
chromosomes
Homologous chromosomes:
What is a ‘locus’?
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Locus (plural-loci):
position of a gene on a chromosome
Homologous chromosomes Non homologous
chromosomes
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AllelesHomozygous :
having the same two alleles at that gene locus
AA or aa
Genotype: RR aa BbHeterozygous
R a b
R a B
Gene loci
Recessiveallele
Dominant allele
Homozygousfor thedominant allele
Homozygousfor therecessive allele
Heterozygous : having dissimilar
alleles at that gene locus
Aa
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Genotype & Phenotype
genotype: total set of alleles of an individualDescribe the following:
homozygous dominantheterozygoushomozygous recessive
phenotype: outward appearance of an individual
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Question: [MAY, 2006]
This question is concerned with genetic inheritance.
1. How does the genotype of an organism determine its phenotype? (1)The genotype determines the proteins made by the body which in turn regulate reactions. Products of reactions determine characteristics expressed.
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Recessive & Dominant Alleles
Recessive allele: expressed only when present in the homozygous condition
Dominant allele: expressed both in the homozygous and heterozygous
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What is meant by:
An autosomal dominant allele: the allele is carried on an autosome & is
expressed in both in the homozygous and heterozygous condition
A recessive sex-linked allele: the allele is carried on a sex chromosome
& is expressed only in the homozygous condition
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Human karyotypeAutosomes set 1 -22
Sex chromosomes set 23
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OverviewA) Monohybrid InheritanceB) Dihybrid InheritanceC) The test crossD) Autosomal dominant and autosomal recessive
pedigree chartsE) LinkageF) Sex determinationG) Alleles and their interactions – multiple alleles,
incomplete dominance, codominanceH) Gene interactions – polygenic inheritance, epistasis
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Monohybrid inheritance:inheritance of a single characteristic
F1 offspring of a monohybrid cross of true-breeding strains resemble only one of the parents.
WHY?
Smooth seeds (allele S) are completely dominant to wrinkled seeds (allele s).
ss
Ss
SS
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F1 x F1 crosses :
Mendel discovered that traits that disappear in the F1 generation reappear in the F2 generation in a 3:1 ratio.
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Which is the dominant allele?
P generation(true-breedingparents)
F1 generation
F2 generation
Purple flowers White flowers
All plants havepurple flowers
Fertilisationamong F1 plants(F1 F1)
3/4 of plantshave purple flowers
1/4 of plantshave white flowers
Allele for purple colour
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What is meant by ‘true-breeding?
P generation(true-breedingparents)
F1 generation
F2 generation
Purple flowers White flowers
All plants havepurple flowers
Fertilisationamong F1 plants(F1 F1)
3/4 of plantshave purple flowers
1/4 of plantshave white flowers
Alleles are the same
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Reginald Crundall Punnett (1875-1967)
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The monohybrid ratio:the ratio of dominant phenotypes to
recessive phenotypes of 3:1
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Mendel’s first law of heredity or the Law of segregation
(separation):
When any individual produces gametes, the alleles separate, so that each gamete receives
only one member of the pair of alleles.
Gametes:
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OverviewA) Monohybrid Inheritance
B) Dihybrid InheritanceC) The test crossD) Autosomal dominant and autosomal recessive
pedigree chartsE) LinkageF) Sex determinationG) Alleles and their interactions – multiple alleles,
incomplete dominance, codominanceH) Gene interactions – polygenic inheritance, epistasis
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Dihybrid Inheritance
the inheritance of two separate traits in a single cross
for example: RRYY x rryy
Let:R represent round seed r represent wrinkled seedY represent yellow seedy represent green seed
Seed shape
Seed colour
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Parental Phenotypes: Round, yellow seeds
Wrinkled, green seeds
Parental genotypes: RRYY rryyx
x
R R Y Y r r y y
Gametes: R Y
F1 genotypes:
F1 phenotypes: 100% round, yellow seeds
x r y
R r Y y
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How to write the gametes:
R rYy
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If two RrYy plants are crossed, the F2 generation would be:-
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY
Ry
rY
ry
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY R
Ry
rY
ry
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RR
Ry
rY
ry
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRY
Ry
rY
ry
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRYY
Ry
rY
ry
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRYY RRYy RrYY RrYy
Ry RRYy RRyy RrYy Rryy
rY RrYY RrYy rrYY rrYy
ry RrYy Rryy rrYy rryy
What is the phenotypic ratio?
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRYY RRYy RrYY RrYy
Ry RRYy RRyy RrYy Rryy
rY RrYY RrYy rrYY rrYy
ry RrYy Rryy rrYy rryy
R - round seed r - wrinkled
seedY - yellow seedy - green seed
F2 phenotypes:
round yellow : R_Y_ round green : R_yy wrinkled yellow : rrY_ wrinkled green : rryy
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRYY RRYy RrYY RrYy
Ry RRYy RRyy RrYy Rryy
rY RrYY RrYy rrYY rrYy
ry RrYy Rryy rrYy rryy
F2 phenotypes:
round yellow : R_Y_ round green : R_yy wrinkled yellow : rrY_ wrinkled green : rryy
R - round seed r - wrinkled seedY - yellow seedy - green seed
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRYY RRYy RrYY RrYy
Ry RRYy RRyy RrYy Rryy
rY RrYY RrYy rrYY rrYy
ry RrYy Rryy rrYy rryy
F2 phenotypes:
round yellow : R_Y_ round green : R_yy wrinkled yellow : rrY_ wrinkled green : rryy
R - round seed r - wrinkled seedY - yellow seedy - green seed
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RY
F1 genotypes: RrYy x RrYyGametes: Ry ryrY RY Ry ryrYx
♂♀ RY Ry rY ry
RY RRYY RRYy RrYY RrYy
Ry RRYy RRyy RrYy Rryy
rY RrYY RrYy rrYY rrYy
ry RrYy Rryy rrYy rryy
F2 phenotypes:
9 round yellow : R_Y_3 round green : R_yy3 wrinkled yellow : rrY_1 wrinkled green : rryy
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Dihybrid Ratio
The phenotype ratio: 9 : 3 : 3 : 1
1) Parents are BOTH heterozygous for both genes.
This ratio indicates:
2. The two genes are on separate chromosomes.
x
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Mendel’s second law or the Law of independent assortment
Alleles of different genes assort independently of one another during gamete formation
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When does Mendel’s second law apply and when does it not ?
It applies to genes that lie on separate chromosomes.
It does not apply when genes lie on the same chromosome.
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1. In the edible pea, tall (T) is dominant to short (t), and green pods (G) are dominant to yellow pods (g). For the following crosses:
i) List the types of gametes;ii) Write the offspring genotypes;iii) Write the phenotypic ratios.
a) TtGg x TtGgb) TtGg x TTGGc) TtGg x Ttgg
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a) Tall – TShort – tGreen pods – GYellow pods – g
TG Tg tG tg
TG
Tg
tG
tg
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a) Tall – TShort – tGreen pods – GYellow pods – g
TG Tg tG tg
TG TTGG TTGg TtGG TtGg
Tg TTGg TTgg TtGg Ttgg
tG TtGG TtGg ttGG ttGg
tg TtGg Ttgg ttGg ttgg
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a) Tall – TShort – tGreen pods – GYellow pods – g
F1 phenotypes:
tall green : T_G_ tall yellow : T_gg short green: ttG_ short yellow : ttgg
TG Tg tG tg
TG TTGG TTGg TtGG TtGg
Tg TTGg TTgg TtGg Ttgg
tG TtGG TtGg ttGG ttGg
tg TtGg Ttgg ttGg ttgg
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a) Tall – TShort – tGreen pods – GYellow pods – g
TG Tg tG tg
TG TTGG TTGg TtGG TtGgTg TTGg TTgg TtGg TtggtG TtGG TtGg ttGG ttGgtg TtGg Ttgg ttGg ttgg
F1 phenotypes:
9 tall green : T_G_ 3 tall yellow : T_gg 3 short green : ttG_ 1 short yellow : ttgg
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b) Tall – TShort – tGreen pods – GYellow pods – g
TG Tg tG tg
TG
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b) Tall – TShort – tGreen pods – GYellow pods – g
TG Tg tG tg
TG TTGG TTGg TtGG TtGg
F1 phenotypes:
all tall green
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Tg tg
TG
Tg
tG
tg
c) Tall – TShort – tGreen pods – GYellow pods – g
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Tg tg
TG TTGg TtGg Tg TTgg Ttgg tG TtGg ttGg tg Ttgg ttgg
c) Tall – TShort – tGreen pods – GYellow pods – g
F1 phenotypes:
3 tall green : T_G_ 3 tall yellow : T_gg 1 short green : ttG_ 1 short yellow : ttgg
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OverviewA) Monohybrid InheritanceB) Dihybrid Inheritance
C) The test crossD) Autosomal dominant and autosomal recessive
pedigree chartsE) LinkageF) Sex determinationG) Alleles and their interactions – multiple alleles,
incomplete dominance, codominanceH) Gene interactions – polygenic inheritance, epistasis
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Test CrossWhy is it done?
is a breeding experiment carried out to determine an unknown genotype within one breeding generation
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Test CrossHow is it done?
it is done by crossing an organism of unknown genotype with a homozygous recessive organism
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Test Cross How is a
conclusion drawn?
the phenotypic ratios among offspring are different, depending on the genotype of the unknown parent
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xbb
50% black : 50% brown
x
100% black
bb
BbbbBb
Test Cross: another exampleBlack: B – BB, BbBrown: b - bb
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Test cross with a double recessive
LetS – smooth (seed shape)s – wrinkled (seed shape)Y – yellow (seed colour)y – green (seed colour)
SSYYSSYySsYY SsYy
Smooth seeds, yellow colour
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1) What is the genotype ?
SY sy
Parents: SSYY x ssyyGametes:
F1:SsYy
(100% smooth & yellow )
x
S – smooth (seed shape)s – wrinkled (seed shape)
Y – yellow (seed colour)y – green (seed colour)
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1) Genotype is homozygous for both alleles (100%)
SY sy
Parents: SSYY x ssyyGametes:
F1:SsYy
(100% smooth & yellow )
x
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2) What is the genotype?
SY
Parents: SsYy x ssyyGametes:
F1:
Sy sysY sy
SsYy Ssyy ssYy ssyy
1/4 smooth :& yellow
1/4 smooth :& green
1/4 w rinkled :& yellow
1/4 w rinkled& green
x
S – smooth (seed shape)s – wrinkled (seed shape)
Y – yellow (seed colour)y – green (seed colour)
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2) Genotype is heterozygous for both alleles (1:1:1:1)
SY
Parents: SsYy x ssyyGametes:
F1:
Sy sysY sy
SsYy Ssyy ssYy ssyy
1/4 smooth :& yellow
1/4 smooth :& green
1/4 w rinkled :& yellow
1/4 w rinkled& green
x
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3) What is the genotype ?
SY
Parents: SSYy x ssyyGametes:
F1:
Sy sy
SsYy Ssyy
1 smooth :& yellow
1 smooth& green
x
S – smooth (seed shape)s – wrinkled (seed shape)Y – yellow (seed colour)y – green (seed colour)
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3) Genotype is homozygous for smooth and heterozygous for yellow (1:1)
SY
Parents: SSYy x ssyyGametes:
F1:
Sy sy
SsYy Ssyy
1 smooth :& yellow
1 smooth& green
x
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SY
Parents: SsYY x ssyyGametes:
F1:
sY sy
SsYy ssYy
1 smooth :& yellow
1 w rinkled& yellow
x
4) What is the genotype?
S – smooth (seed shape)s – wrinkled (seed shape)
Y – yellow (seed colour)y – green (seed colour)
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4) Genotype is heterozygous for smooth and homozygous for yellow (1:1)
SY
Parents: SsYY x ssyyGametes:
F1:
sY sy
SsYy ssYy
1 smooth :& yellow
1 w rinkled& yellow
x
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OverviewA) Monohybrid InheritanceB) Dihybrid InheritanceC) The test cross
D) Autosomal dominant and autosomal recessive pedigree charts
E) LinkageF) Sex determinationG) Alleles and their interactions – multiple alleles,
incomplete dominance, codominanceH) Gene interactions – polygenic inheritance, epistasis
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some human traits are controlled by a single gene
some of these exhibit: dominant inheritance recessive inheritance
PEDIGREE ANALYSIS
Pedigree analysis is used to track inheritance patterns in families
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What does a PEDIGREE CHART show?
the phenotypes of individuals in several generations of a family, and provides a basis for attempting to determine their genotype
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What does ‘wild type’ mean?
The most common phenotype in the
population
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K ey:A A = affectedA a = affectedaa = norm al
= norm al fem ale
= norm al m ale
= affected fem ale
= affected m ale
A a A a
aa A a aa aaaaA ?
A a aaA a aa aaaa
P aren tal generation
F1 generation
F2 generation
Autosomal dominant disorders
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Autosomal dominant disorders
1. Affected children usually have an affected parent.
A A
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Autosomal dominant disorders
2. Heterozygotes (Aa) are affected.
A A
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Autosomal dominant disorders
3. Two affected parents can produce an unaffected child.
A A
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Autosomal dominant disorders
4. Two unaffected parents will not have affected children.
A A
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aa A ?
A a A ?A a
A a A a A?A?
K eyaa = affectedA a = carrier (appears norm al)A A = norm al
A ?
aa A?aa
Autosomal recessive disorders
Albinos
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Autosomal recessive disorders
1. Most affected children have normal parents.
aa A ?
A a A ?A a
A a A a A?A?
K eyaa = affectedA a = carrier (appears norm al)A A = norm al
A ?
aa A?aa
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aa A ?
A a A ?A a
A a A a A?A?
K eyaa = affectedA a = carrier (appears norm al)A A = norm al
A ?
aa A?aa
Autosomal recessive disorders
2. Heterozygotes (Aa) have a normal phenotype.
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Autosomal recessive disorders
3. Two affected parents will always have affected children.
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Autosomal recessive disorders
4. Affected individuals with homozygous normal mates will have normal children.
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aa A ?
A a A ?A a
A a A a A?A?
K eyaa = affectedA a = carrier (appears norm al)A A = norm al
A ?
aa A?aa
Autosomal recessive disorders
5. Close relatives who reproduce are more likely to have affected children.
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Categories of inheritance
1. Autosomal recessive– e.g. albinism
2. Autosomal dominant– e.g. Huntington’s Disease [degeneration of
brain cells]
3. X-linked recessive– e.g. color-blindness, haemophilia
4. X-linked dominant [Very Rare]– e.g. hypophosphatemia [low level of
phosphate in blood]
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When working genetics problems:
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The probability that two independent events will
both occur is the product of their individual probabilities.
e.g. What is the probability that a child is a MALE with BROWN EYES if both parents are heterozygous? Brown is dominant to blue eyes.
Multiply probability of being a male by probability of having brown eyes.
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Probability of having BROWN EYES.
Probability of being a MALE:
0.5 or 50%
0.75 or 75%
0.5 x 0.75 = 0.375 or 37.5%
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Question: [SEP, 2011]
The pedigree diagram shown in Figure 1 below follows the inheritance of Marfan syndrome, a disorder of connective tissue in humans that affects males and females equally. The allele for Marfan syndrome, M, is dominant to the allele, m, for unaffected (normal) connective tissue. In the diagram below, individuals affected with Marfan syndrome are represented by shaded symbols whilst unaffected individuals are represented by unshaded symbols. Males are represented as squares and females as circles.
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Figure 1: Pedigree diagram showing inheritance of Marfan Syndrome across three generations.
1.1 Use the diagram in Figure 1 to deduce the genotype of all the individuals represented. Insert your answers in the table below:
= affected female
= affected male
= normal female
= normal male
M: MM, Mm
m: mm
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= affected male
= normal female
= normal male
M: MM, Mm
m: mm
Individual GenotypeI-1 mmI-2 MmII-1 MmII-2 mmII-3 MmII-4 mmII-5 mmIII-1 MmIII-2 MmIII-3 Mm
mm
mmmmmm
= affected female
Mm
MmMm
Mm
Mm
Mm
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1.2 Assume that individual III-3 mates with an affected male. What is the probability that this cross would produce an affected female? Your working is to be shown. (2)
Individual III-3 (Mm) mates with an affected male (MM): Mm x MM = MM and Mmprobability to produce a female is: 0.5 probability to be affected is 1So, 0.5 x 1 = 0.5
Individual III-3 (Mm) mates with an affected male (Mm): Mm x Mm = MM Mm Mm mm
probability to produce a female is 0.5 probability to be affected is 0.75 So, 0.5 x 0.75 = 0.375
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1.3 What is the probability that the cross referred to in the previous question would produce an unaffected male? Your working is to be shown. (2)
Individual III-3 (Mm) mates with an affected male (MM): Mm x MM = MM and Mmprobability to be unaffected (mm) is 0
Individual III-3 (Mm) mates with an affected male (Mm): Mm x Mm = MM Mm Mm mmprobability to produce a male is 0.5 probability to be unaffected (mm) is 0.25So, 0.5 x 0.25 = 0.125
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