This document discusses various concepts related to genetics and inheritance patterns. It begins by defining key terms like autosomes, sex chromosomes, sex linkage, and sex-linked traits. It provides examples of sex-linked traits in humans like color blindness. The document then discusses concepts such as sex-linked dominance and inheritance patterns seen in reciprocal crosses. It also covers sex-influenced and sex-limited traits. In summary, the document is a comprehensive review of genetics topics focusing on inheritance patterns related to sex chromosomes and the influence of sex on trait expression.
This presentation intends to explore the sex-linked characters along with some fatal diseases of human beings, their cause, consequences and other issues.
There are two types of chromosomes, Autosomes and Sex chromosomes
Autosomes are those chromosomes that are not involved in sex determination.
Sex chromosomes are those chromosomes that determine the sex of an organism.
A human somatic cell has two sex chromosomes: XY in male (hetero-gametic) and XX in female (homo-gametic).
Concept of Sex chromosomes and autosomes,
Inheritance of X- linked genes – eye colour in Drosophila,
Inheritance of colour blindness in humans,
Inheritance of Y-linked Genes -Holandric genes in humans,
Sex influenced genes – baldness in humans
Sex-limited genes - feathering in domestic fowl
This presentation intends to explore the sex-linked characters along with some fatal diseases of human beings, their cause, consequences and other issues.
There are two types of chromosomes, Autosomes and Sex chromosomes
Autosomes are those chromosomes that are not involved in sex determination.
Sex chromosomes are those chromosomes that determine the sex of an organism.
A human somatic cell has two sex chromosomes: XY in male (hetero-gametic) and XX in female (homo-gametic).
Concept of Sex chromosomes and autosomes,
Inheritance of X- linked genes – eye colour in Drosophila,
Inheritance of colour blindness in humans,
Inheritance of Y-linked Genes -Holandric genes in humans,
Sex influenced genes – baldness in humans
Sex-limited genes - feathering in domestic fowl
In Drosophila melanogaster, the yellow body gene is X-linked. The yel.pdfarhamgarmentsdelhi
In Drosophila melanogaster, the yellow body gene is X-linked. The yellow body phenotype is
recessive to brown body phenotype. A yellow body female fruit fly was mated to a brown body
male. The vast majority of the male progeny are yellow body. However, a rare brown body male
was found in the progeny (1 out of 2060 males). What is the likely karyotype of this brown body
son? XXY XX XYY XO XXX
Solution
Sex inheritance by modified Mendelian mechanism:
X-linked inheritance means that the gene causing the trait or the disorder is located on the X
chromosome.
X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X
chromosome causes the phenotype to be expressed in males who are necessarily hemizygous for
the gene mutation because they have one X and one Y chromosome. Carrier females who have
only one copy of the mutation do not usually express the phenotype,
Females are XX (homogametic)
Males are XY (heterogametic)
Body color inherited by single gene, two allele system, brown dominant to yellow
But, sex and body color not inherited independently
Body color is linked to sex
Body color gene on X chromosome
Therefore, males have only one body color allele: Haploid and females have two eye color
alleles: Diploid.
Normally all the sons and none of the daughters show the recessive sex-linked characters of the
mother when the father carries the dominant allelomorph. For example, a yellow body female
mated to a brown body male produces yellow body males and brown body females, but rarely
also a yellow body female or a brown body son. The production of these exceptions by a normal
XX female must be due to an aberrant reduction division at which the two X chromosomes fail
to disjoin from each other. In consequence both remain in the egg or both pass into the polar
body. In the latter case an egg without an X chromosome is produced. Such an egg fertilized by
an X sperm produces a male with the constitution XO. These males received their single X from
their father and therefore show the father\'s characters. But that the Y does play some positive
role is proved by the fact that all the XO males have been found to be absolutely sterile.
Answer is d) XO.
Consider the following pedigree, which traces the inheritance of a si.pdfdeepaarora22
Consider the following pedigree, which traces the inheritance of a single-gene hereditary
disease. Only individuals that are either affected or normal are shown. In other words, potential
heterozygotes are NOT indicated. Characterize each of the following modes of inheritance as:
impossible, unlikely, or probable. Justify your answers. Autosomal dominant Autosomal
recessive X-linked dominant X-Iinked recessive Y linked
Solution
Single gene herediary diseases are mainly caused by a change of any one gene in a particular
DNA.Its divided into diiferemt categories like dominant ,recessive and X linked.Square indicates
a male and circle female.According to the diagram affected male is crossed with an unaffected
female.The progeny obtained is affected daughters and unaffected sons.
Autosomal dominant: in this case, the father — has a 50 percent chance of having an affected
child with one mutated gene (dominant gene) and a 50 percent chance of having an unaffected
child with two normal genes (recessive genes).But, in our case none of the sons are affected
which means its criss cross inheritance that is from father to daughter.Hence , this case is
unlikely
Autosomal recessive:To have an autosomal recessive disorder, you inherit two mutated genes,
one from each parent. These disorders are usually passed on by two carriers.The cross given in
the question is not between the two carriers.The male parent is affected for sure hence this case is
impossible
X linked dominant:As in autosomal dominant inheritance, only one copy of a disease allele on
the X chromosome is required for an individual to be susceptible to an X-linked dominant
disease.Both males and females can be affected, although males may be more severely affected
because they only carry one copy of genes found on the X chromosome. Some X-linked
dominant disorders are lethal in males.When a female is affected, each pregnancy will have a
one in two (50%) chance for the offspring to inherit the disease allele. When a male is affected,
all his daughters will be affected, but none of his sons will be affected.So, there are probable
chance for this type of inheritance
X linked recessive:For X-linked recessive disorders, an affected father who has a mutation in a
gene on the X chromosome can transmit either the X chromosome with this mutation or a Y
chromosome to his children. If the mother is not affected or a carrier, none of his sons will be
affected since they can only inherit a normal X chromosome from their mother and they inherit a
Y chromosome from their father. Each daughter will have a 50% chance of being an unaffected
carrier and a 50% chance of both X chromosomes being normal.In our cross all daughters are
affected which means this type of inheritance is impossible
Y linked:This type of inheritance is impossible in this case as all female children are getting
affected.If it would have been Y linked then only sons should have been affected as Y
chromosome is present only in males.Hence this.
Breaking down Biology into simpler bits is the most effective way to learn hence this presentation aims to simplify the concept of 'Linked Inheritance' which makes understanding Inheritance better.
not exaclty sure what to do here U Sexlinked Disorders Se.pdfsaravanan544051
not exaclty sure what to do here
U. Sex-linked Disorders Sex-linked traits ine controlled by genes that are found on the X
clromosome, but not on the Y chromosome in humans. The X chromosome is larger and has more
genes than the Y chromosome. This complicntes the inleritance of uraits on the X clromosome
since we expect that a normal diploid cell will have two alleles for any gene. Such is not he case
for males siuce they are XY and will only have cne copy of the genes that are locied ou the X
chromosome: Females (XX) will have two ulleles for a gene located on the X chromosome Males (
XY) will only have one allele for that trait. This, females with one dominant and one recessive
allele for a gene on the X chromosene would display the dominant phenotype. However a mate
will always displey the phenorype of the one allele that they have for the mait that is carried on the
X chroinosonie. A new way of writing alleles: XR - normal eyesiglt X-colorblind Genotypes: XRXR
XRXrXRYXRXrXY Phenotypes: Normal Eyesight and Colorblind Remember to follow the same
steps in order to solve problems: 1. Assign lefters to represent the genes 2. Determine the
parental phenotypes and genotypes. 3. Predict the outcome of a cross between the possible
gameles from the tiro parents. 4. State plenotypic and genoty pic ratios present ia the offspring. 5.
Don't forget to answer the question witlin the problem. ains. begin{tabular}{|c|c|} hlinex & x hlinexn
x & xx hlinexy & xy hline end{tabular}.
Heredity or Hereditary is the process of passing the traits and characteristics from parents to offsprings.
The offspring cells get their features and characteristics aka genetic information from their mother and father.
In Drosophila melanogaster, the yellow body gene is X-linked. The yel.pdfarhamgarmentsdelhi
In Drosophila melanogaster, the yellow body gene is X-linked. The yellow body phenotype is
recessive to brown body phenotype. A yellow body female fruit fly was mated to a brown body
male. The vast majority of the male progeny are yellow body. However, a rare brown body male
was found in the progeny (1 out of 2060 males). What is the likely karyotype of this brown body
son? XXY XX XYY XO XXX
Solution
Sex inheritance by modified Mendelian mechanism:
X-linked inheritance means that the gene causing the trait or the disorder is located on the X
chromosome.
X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X
chromosome causes the phenotype to be expressed in males who are necessarily hemizygous for
the gene mutation because they have one X and one Y chromosome. Carrier females who have
only one copy of the mutation do not usually express the phenotype,
Females are XX (homogametic)
Males are XY (heterogametic)
Body color inherited by single gene, two allele system, brown dominant to yellow
But, sex and body color not inherited independently
Body color is linked to sex
Body color gene on X chromosome
Therefore, males have only one body color allele: Haploid and females have two eye color
alleles: Diploid.
Normally all the sons and none of the daughters show the recessive sex-linked characters of the
mother when the father carries the dominant allelomorph. For example, a yellow body female
mated to a brown body male produces yellow body males and brown body females, but rarely
also a yellow body female or a brown body son. The production of these exceptions by a normal
XX female must be due to an aberrant reduction division at which the two X chromosomes fail
to disjoin from each other. In consequence both remain in the egg or both pass into the polar
body. In the latter case an egg without an X chromosome is produced. Such an egg fertilized by
an X sperm produces a male with the constitution XO. These males received their single X from
their father and therefore show the father\'s characters. But that the Y does play some positive
role is proved by the fact that all the XO males have been found to be absolutely sterile.
Answer is d) XO.
Consider the following pedigree, which traces the inheritance of a si.pdfdeepaarora22
Consider the following pedigree, which traces the inheritance of a single-gene hereditary
disease. Only individuals that are either affected or normal are shown. In other words, potential
heterozygotes are NOT indicated. Characterize each of the following modes of inheritance as:
impossible, unlikely, or probable. Justify your answers. Autosomal dominant Autosomal
recessive X-linked dominant X-Iinked recessive Y linked
Solution
Single gene herediary diseases are mainly caused by a change of any one gene in a particular
DNA.Its divided into diiferemt categories like dominant ,recessive and X linked.Square indicates
a male and circle female.According to the diagram affected male is crossed with an unaffected
female.The progeny obtained is affected daughters and unaffected sons.
Autosomal dominant: in this case, the father — has a 50 percent chance of having an affected
child with one mutated gene (dominant gene) and a 50 percent chance of having an unaffected
child with two normal genes (recessive genes).But, in our case none of the sons are affected
which means its criss cross inheritance that is from father to daughter.Hence , this case is
unlikely
Autosomal recessive:To have an autosomal recessive disorder, you inherit two mutated genes,
one from each parent. These disorders are usually passed on by two carriers.The cross given in
the question is not between the two carriers.The male parent is affected for sure hence this case is
impossible
X linked dominant:As in autosomal dominant inheritance, only one copy of a disease allele on
the X chromosome is required for an individual to be susceptible to an X-linked dominant
disease.Both males and females can be affected, although males may be more severely affected
because they only carry one copy of genes found on the X chromosome. Some X-linked
dominant disorders are lethal in males.When a female is affected, each pregnancy will have a
one in two (50%) chance for the offspring to inherit the disease allele. When a male is affected,
all his daughters will be affected, but none of his sons will be affected.So, there are probable
chance for this type of inheritance
X linked recessive:For X-linked recessive disorders, an affected father who has a mutation in a
gene on the X chromosome can transmit either the X chromosome with this mutation or a Y
chromosome to his children. If the mother is not affected or a carrier, none of his sons will be
affected since they can only inherit a normal X chromosome from their mother and they inherit a
Y chromosome from their father. Each daughter will have a 50% chance of being an unaffected
carrier and a 50% chance of both X chromosomes being normal.In our cross all daughters are
affected which means this type of inheritance is impossible
Y linked:This type of inheritance is impossible in this case as all female children are getting
affected.If it would have been Y linked then only sons should have been affected as Y
chromosome is present only in males.Hence this.
Breaking down Biology into simpler bits is the most effective way to learn hence this presentation aims to simplify the concept of 'Linked Inheritance' which makes understanding Inheritance better.
not exaclty sure what to do here U Sexlinked Disorders Se.pdfsaravanan544051
not exaclty sure what to do here
U. Sex-linked Disorders Sex-linked traits ine controlled by genes that are found on the X
clromosome, but not on the Y chromosome in humans. The X chromosome is larger and has more
genes than the Y chromosome. This complicntes the inleritance of uraits on the X clromosome
since we expect that a normal diploid cell will have two alleles for any gene. Such is not he case
for males siuce they are XY and will only have cne copy of the genes that are locied ou the X
chromosome: Females (XX) will have two ulleles for a gene located on the X chromosome Males (
XY) will only have one allele for that trait. This, females with one dominant and one recessive
allele for a gene on the X chromosene would display the dominant phenotype. However a mate
will always displey the phenorype of the one allele that they have for the mait that is carried on the
X chroinosonie. A new way of writing alleles: XR - normal eyesiglt X-colorblind Genotypes: XRXR
XRXrXRYXRXrXY Phenotypes: Normal Eyesight and Colorblind Remember to follow the same
steps in order to solve problems: 1. Assign lefters to represent the genes 2. Determine the
parental phenotypes and genotypes. 3. Predict the outcome of a cross between the possible
gameles from the tiro parents. 4. State plenotypic and genoty pic ratios present ia the offspring. 5.
Don't forget to answer the question witlin the problem. ains. begin{tabular}{|c|c|} hlinex & x hlinexn
x & xx hlinexy & xy hline end{tabular}.
Heredity or Hereditary is the process of passing the traits and characteristics from parents to offsprings.
The offspring cells get their features and characteristics aka genetic information from their mother and father.
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2. Title of important books:
Principles of Genetics by Gardner, Simmions and Snustad.
Fundamental of Genetics by B.D.Singh
A Textbook of Animal Genetics by P.Kanakraj
Introduction to Veterinary Genetics by F.W.Nicholas
Animal Genetics: concept and implication by Gurvinder
Singh
The Genetics of Populations by J.L.Lush
Introduction to Quantitative Genetics by D.S. Falconer
3. There are two types of chromosomes,
Autosomes and Sex chromosomes
Autosomes are those chromosomes that are not involved
in sex determination.
Sex chromosomes are those chromosomes that determine
the sex of an organism.
A human somatic cell has two sex chromosomes: XY in
male (hetero-gametic) and XX in female (homo-gametic).
In birds the female (ZW) is hetero-gametic and male (ZZ)
is homo-gametic.
Ordinarily, F1 and F2 generations from reciprocal crosses
yield identical results and it does not matter if the female or
male parent had the recessive character. Further male and
females in the progeny show identical ratios.
4. This ratio change in reciprocal cross due to
phenomenon of sex linkage.
Sex linkage is an association of a character with sex of
the progeny during inheritance.
Sex linkage refers to the association of a hereditary trait
with sex chromosomes.
Most genes for sex link traits are present only on the X-
chromosome. The Y-chromosome is smaller (Very few
genes are located on Y chromosome).
Because of their location in the sex chromosomes, they
are said to be “sex linked traits”.
5. Certain sex linked genes are located only on X
chromosomes (in XY system) or on the Z chromosome
(ZW system) and their alleles are absent from Y
chromosome.
Characters for which genes are located on sex on X
chromosomes are known as sex linked traits.
Genes controlling these traits are called sex linked
genes.
Linkage of such genes is referred to as sex linkage.
Inheritance of such genes or characters is known as sex
linked inheritance.
X-linked inherited diseases occur more frequently in
males because they only have one X chromosome.
6. X linked inheritance may be X - linked dominant, X-linked
recessive or X - linked co dominant.
Sex linked genes show the dominance recessive
relationship only in homogametic sex (e.g. female in
humans) because it can carry two alleles at the sex linked
locus. So, female can be homozygous or heterozygous.
In the heterogametic sex (males in humans and females in
birds) do not show dominance recessive relationship
because the existence of only a single X or Z
chromosome.
The term hemizygous is used for X linked gene in males
as they carry only one allele with regard to sex linked trait
(In birds the female is hemizygous).
7. Pseudo-dominance is phenomenon in which a single
copy of recessive allele is phenotypically expressed
because a second copy of the gene is absent. This
pseudo dominance found in male in humans and in
female in birds because they are hemizygous.
8. The frequency of individuals showing a recessive sex
linked trait is markedly higher in heterogametic sex than
that in the homogametic sex.
The gene governing the sex linked traits are not
transmitted from male parent to directly their male
progeny. e.g. white eye gene is not transmitted from
male to male in drosophila fly.
The sex linked gene are located on X chromosomes
only but not present on Y chromosome
9. Inheritance of sex linked characters does not follow
normal segregation pattern.
In human and drosophila fly, male transmits its sex
linked genes to all its daughters.
These daughters transmit this gene to half of their male
progeny.
As a result, a sex linked recessive gene is transmitted
from male to its female progeny and then to half of
male progeny of such females.
Thus the sex linked genes pass from male female
and then back to male, this type inheritance pattern is
called as criss-cross inheritance pattern.
10. In X-linked dominance, both males and females can
display the trait or disorder by having only one copy of
the allele. E.g. barred pattern in poultry.
In X-linked recessive, male can display the trait by
having only one copy allele but in female it display when
both recessive alleles are present Examples are:
Eye color in drosophila
Colour blindness in Human
Haemophilia in Human
Feather pattern in poultry
Rate of feathering in poultry
Down colour pattern in poultry
Thomas Hunt Morgan (1910) observed a male
Drosophila melanogaster with white eyed (mutant)
mated fly with a red eyed (Normal) female and got the
following result. (As per mention in figures)
11.
12.
13. In F2 generation, equal number of red and white eyed
individuals with normal sex ratio appeared. (That finding
different from normal autosomal gene inheritance in
which there is no difference in reciprocal crosses). The
white-eye colour gene is located on the X-chromosome.
14.
15. Males have only one X chromosome, a single
recessive allele on that X chromosome will act as
pseudo dominance and cause the disease.
Females have two X chromosome, so two copies of the
recessive allele are required for the disease to express
in females.
Males never pass the disease to their sons because
there is no male-to-male transmission of the X
chromosome.
Males pass the defective X chromosome to all of their
daughters, who are described as obligate carriers.
16. Transmission of the sex linked disease from affected
males to male grand children through carrier daughters is
described as a "Nasse's Law".
Female carriers pass the defective X chromosome to half
their sons.
17. Haemophilia
It is a hereditary defect which is governed by recessive
gene and is inherited through females.
In case of a marriage between hemophilic woman and
normal man, the disease will be transmitted to 50% of the
sons even if the gene is in heterozygous condition in the
carrier.
18. Parents Haemophilic
woman
Normal man
Genotypes XhXh XHY
Sperms
XH Y
Ovum X
h
XHXh
(Normal)
XhY
(haemophilic)
Parents Normal woman Haemophilic
man
Genotyp
es
XHXH XhY
Sperms
Xh Y
Ovum
XH XHXh
(Normal)
XHY
(Normal)
XH XHXh
(Normal)
XHY
(Normal)
Normal but Carrier for haemophilia
19. Colour blindness
This trait is governed by a recessive gene located on X
chromosome.
A person having such defect cannot differentiate between
red and green colour.
Sons from the marriage between colour blind man and
normal woman will be normal, but daughters will carry
such genes in heterozygous condition.
Marriage of such carrier girl with colour blind boy will
produce children in which both male and female children
will be colour blind each in 50% cases.
20.
21.
22. Sex linked dominance
Sex linkage in poultry
In poultry, female individual is heterogametic having only
one X-chromosome (XO condition) and male is
homogametic having two X-chromosomes (XX).
Therefore, inheritance pattern in relation to sex will be
reversed in this case.
Barred plumage is a popular example of sex linked
character in poultry. In an individual, which has barred
plumage, feathers are banded with bars of black on a
white background.
23. Barred ♀ x Non barred ♂
If barred (BW) female individual is crossed with non
barred male (bb) individual, (barred is normal and
dominant over non barred), only barred males and non
barred females are obtained in F1 generation.
In F2 generation, barred and non barred individuals
appear in 1 : 1 ratio, among male as well as female
populations.
Non barred ♀ x barred ♂
When non barred female individual (bW) is crossed
with barred male (BB), all progeny (male as well as
female) would be barred in F1 generation.
In F2 generation 50 % females will be barred and rest
50 % non barred while all males would be barred.
24. Male
Gametes
Female Gametes
B W
b Bb
Barred
Male
bW
Non barred
Female
Female
Gametes
Male Gametes
B b
b Bb
Barred
Male
bb
Non Barred
Male
W BW
Barred
Female
bW
Non Barred
Female
1:1 = Barred: Non barred
1:1 = Barred: Non barred
50 % barred : 50% non barred
50% male barred & 50% male non barred
50% female barred & 50% female non barred
F2 Generation
25. Male
Gametes
Female Gametes
b W
B Bb
Barred
Male
BW
Barred
Female
Female
Gametes
Male Gametes
B b
B BB
Barred
Male
Bb
Barred Male
W BW
Barred
Female
bW
Non Barred
Female
100% barred
3:1 = Barred: Non barred
100% male barred
50% female barred & 50% female non barred
F2 Generation
26. Genes Linked with Y Chromosome
Non-homologous portion of Y chromosome contains few
genes.
Two genes appear to be located in this region in Drosophila
for male fertility.
Seventeen genes are present in the non-homologous
portion of human Y chromosome.
Genes which are present in Y chromosome are known as
holandric genes.
The best example of holandric condition is presence of
excessive hair on ears in man, the condition is known as
hypertrichasis, which is a Y linked character.
Y-linked genes would be transmitted directly from father to
son and never appears in female. Examples are :
27. Histocompatability gene (H-Y) present on the short
arm of human Y - chromosome.
SRY (Sex-determining Region Y) genes.
The hair on pinna of the ear in man has been
interpreted as due to holandric gene.
28. Features of sex-linked recessive diseases
The frequency is higher in heterogametic than
homogametic sex.
It is transmitted from affected man through normal
daughter to half of the grandsons.
Does not occur in a woman unless her father has it.
All the sons of the woman having this trait are
affected.
Features of sex-linked dominant diseases
More common in females.
All female offspring of affected male will be affected
If mother is normal sons will not be affected with the
diseases.
29. Sexing of day old chicks
Auto-sexing is method of sexing in day old chicks by their
different appearances when they have hatched.
The chicks are sexed at hatching as poultry
farmers/breeders are interested to keep only the female
chicks for egg production in future.
In traditional method of sexing is vent method (Japanese
method).
Time consuming, Laborious, Expensive and require
experience
While the sexing by sex linkage is less expensive, more
accurate more convenient.
30. In birds (butterflies, silkworm, moths, fishes) males are
homogametic (ZZ) and females are heterogametic (ZW).
The 'barring' pattern is sex-linked. That is the males have
two chromosomes for barring and the females only one
chromosome resulting in to, a day old chicks have a light
coloured patch on the top of the head.
When these light coloured patches are combined with
brown colour, there is a very clearly defined stripe the
body.
31. The male chicks on the other-hand have a light patch
covering most of the head and there is only a very
blurred resulting in to unclear body stripe.
The first auto-sexing breed was developed and
described by Punnett and Pease (1930).
Some autosexing traits in poultry:
• Barred (B) and non-barred (b) plumage pattern in
Plymouth Rock
• Silver plumage (S) in Sussex x Golden plumage (s) in
Rhode Island Red and New Hampshire
• Slow feathering (K) x Fast feathering (k)
32. Reducing cost of broiler chick production:
Sex linked dwarfing gene (dw) offers potential value
by reducing cost of commercial broiler chick
production.
The normal size of hen who used for production of
broiler chicks are heavy and required much feed,
space, excess fat deposition and produce abnormal
eggs. The adult dwarf mother (dw W) weigh 30 %
less than the normal sized hen (Dw W).
When this dwarf (dw W) mother mated with normal
sized male (Dw Dw). The commercial chicks resulting
from this mating have normal size (Dw dw ♂ and Dw
W♀).
33. The traits which are controlled by genes present on
autosomes but whose expression is influenced by the
sex of individual are called sex influence traits.
A trait which is influenced by the sex of the individual is
called sex-influenced trait.
Sex-influenced traits are those that are dominant in one
sex but recessive in the other. This is due to the
different cellular environments in males and females
provided by sex hormones.
Different hormonal environments affect expression of
heterozygote of a trait but homozygotes are unaffected
and express the trait unrelated of the hormones
produced.
Sex Influenced Traits
34. These genes have three main features:
1. Located in the autosomes.
2. Express more frequently in one sex than other.
3. Expression of such characters appears to be
governed by sex hormones
4. No difference between reciprocal crosses in F1 and F2.
5. Dominance in the heterozygous condition depends on
the sex of the individual
35. Coat Colour in Ayershire cattle
Sex
influence
characters
Pattern of baldness in humans
Genotype
Phenotype
Genotype
Phenotype
Bull Cow Man Woman
MM Mahogany Mahogany BB Bald Bald
Mm Red Red Bb Bald Non
bald
mm Red Red bb Non bald Non
bald
36. Example: Horned condition in sheep
Dorset horn – both males and females horned
Suffolk – both males and females hornless (polled)
Dorset (HH) x Suffolk (hh)
Hh Horned if male progeny
Hornless (polled) if female progeny
Horned condition in sheep
Genotype
Phenotype
Male Females
HH horned horned
Hh horned hornless
hh hornless hornless
In F2 Generation
37.
38. Some autosomal genes express characters in only one
sex (either male or female).
These are autosomal genes but can be expressed only
in particular sex. As their expression is limit to only one
sex, they are called sex-limited traits. Or
Those traits whose development is limited to only one
sex are known as sex limited traits.
Sex Limited Traits
39. Main characteristics:
1. They express in one sex only and not in the other
sex.
2. Sex limited genes may be located either in sex
chromosome or autosomes.
3. Sex limited genes control the expression of
primary and secondary sex characters
Examples are:
Milk production in mammals
Egg production in chicken
Genes responsible for secondary sexual characteristics
as well as primary sexual characters like…
Development of Hair, mammary gland etc
Cock-feathering trait in bird
40. Hen- feathering result from a single gene "H" and cock-
feathering result from its allele, "h".
The expression of gene “H” and “h” depends upon the
sex hormones.
The “h” gene produces hen feathering if female hormone
is present, cock-feathering if female hormone is absent.
This was proved by removing the ovaries in female or
testes in male birds, which possesses hen feathered,
results in production of cock feathering eventhough “H”
allele present.
Hen feathered
female (HH or Hh)
Cock feathered
female (HH or Hh)
Removal of Ovary
Hen feathered male
(HH or Hh)
Cock feathered
male (HH or Hh)
Removal of Testes
41.
42. Sex Linked Characters Sex Limited Characters
1 Genes are located on sex or X
chromosomes.
Genes ate located on sex
chromosomes or autosomes.
2 Can express in both the sexes. Express in one sex only.
3 Include characters not related
to sex.
Include primary and secondary
sex characters.
4 Examples- White eye in
Drosophila, Hemophilia and
Colour blindness in man
Examples – Milk production,
Egg Production