HAFIZ M WASEEM
SUBJECT : GENETICS
TOPIC: SEX LINKAGE
 SEX LINKAGE
 HISTORY
 TYPES OF SEX LINKAGE
 SEX LINKAGE IN HUMAN
 COLOUR BLINDNESS
 CAUSES OF COLOUR BLINDNESS
 TYPE OF COLOUR BLINDNESS
 EXAPLE OD COLOUR BLINDNESS
 TEST CROSS
 SYPTOMS
 DETECTION
 EFFECTS
 SEX INFLUENCED TRAIT
 SEX LIMITED TRAIT
 CONCLUSION
DEFINITION:
Sex linkage is the phenotypic expression of
an allele that is independent on he gender of the
individual and is directly tied to sex chromosome.
HISTORY:
THOMAS MORGAN:
Sex linkage was first discovered by Thomas Morgan in 1910
who observed a disproportionate percentage of white- eye male fruits
flies. This experiment involved crossing purebred red-eyed female
fruit flies with these mutant white – eyed males. The result was
exclusively red – eyed individuals of both sexes.
There are some examples of sex linkage.
1. Hemophilia
2. Red- green colour blindness
3. Congenital night blind ness
4. Some high blood pressure genes
5. Fragile X syndrome
HEMOPHILIA
CONGENITAL NIGHT
BLINDNESS
 Twenty genes are sex linked.
 Red green colour blindness and hemophilia
 Both these disease are sex linked recessive trait.
 DEFINITION
Colour blindness is a condition in which
individuals have difficulty in distinguishing red
from green.
 Cats and Dogs
To see in full colour as we know it,
humans use three cones red, blue, and green.
However cats and dogs have only blue and green
cones. This means they have much more muted
perception of colour, which akin to colour
blindness in humans.
 There are three types of colour blindness.
 Protanolay:
 It is a type of o colour blind ness which reduce to red
colour.
 Deuteranomaly
Which reduce sensitivity to green color.
Tritanomaly
Which reduce sensitivity to blue colour.
 E.B Wilson firstly discovered facts about
hereditary color blindness
 It is genetic disease and inherited from mother
to child
 Gene for colour blindness present on X
chromosome
 Colour blindness occurs in about 8% males and
only 0.5% in females
 Some people become colour blind due to other
disease like diabetes and medication and
multiple sclerosis.
 Why blindness colour is occur more in males
instead of females.
 Father transfer his x chromosomes to all
daughter and mother transfer her x
chromosome.
 Son will be colour blind and daughter will be
normal if his mother is carrier father is normal
 Colour blind daughter will be produce only
produce only when his father is colour blind
and mother is carrier or colour blind.
 Since such marriages are very rare.
 If mother is normal father is colour blind
 Then son will be normal and daughter will be
carrier.
TEST CROSS-2
If mother is carrier
and father is colour
blind.
50 percent chances
daughter may be
colour blind or
carrier.
50 percent chances
son will be normal
or colour blind.
TEST CROSS -3
If mother is colour
blind and father is
normal.
All sons will be
colour blind and all
daughter will be
carriers.
 Symptoms of colour blindness could range
from mild to severe.
 Example would be difficult distinguishing
between colors, or inability to see shades of the
same color.
 Rapid eye movement could occur in rare cases,
and sensitivity of bright light.
 They could also suffer from having trouble
seeing the brightness of color in the usual way.
 Inability to tell the difference between the
shades of same or similar colors.
 Particularly red and green or blue or yellow.
 It can be detected by using special charts made up of coloured
dots
 These dots are so arranged that coloured blind person can see a
different patterns
 Sex linked traits in other animals:
 White eyes in drosophila melanogaster flies – the first sex linked
gene discovered.
 Fur colour in domestic cats : the gene that causes orange pigment
is on the X chromosome; thus a calico or tortoiseshell cat, with
both black and orange pigment, is nearly always female.
 The first sex- linked gene ever discovered was the lacticolor X
linked recessive gene in the moth.
 Sex – influenced traits :
 Sex influenced or sex conditioned traits are
phenotypes affected by whether they appear in
a male or female body. Even in a homozygous
dominant or recessive female the condition
may not be expressed fully.
 Example :
The baldness in humans.
 Sex limited traits:
These are characters only expressed in
one sex. They may be caused by gene on either
autosomal or sex chromosome
BALDNESS IN HUMANS
POLYMORPHISM IN
HONEY BEES
 There are no treatments for most types of color
vision difficulties, unless the colour vision
problem is related to the use of certain
medicine or eye condition.
 Discontinuing the medication causing your
vision problem or treating the underlying eye
disease may result in better color vision.
 Morgan’s conclusion was the trait for eye
color must be encoded on the X chromosome,
and that white eyes must represent the
recessive allele.
 References:
 Morgan, Thomas 1919. The physical basis of hereditary
 Genetics home reference (2006), genetic condition illustration,
national library of medicine
 Don caster L.& Raynor G.H 1906. Breeding experiments with
Lepidoptera. Proceeding of the zoological society of London.
 Ford E.B (1965) Genetics polymorphism. p17 – 25.MIT Press1965.
 Mallet J. Joron M. (1999) the evolution diversity in warning color
and mimicry polymorphisms, shifting balance, and speciation.
 Zirkle, Conway (1946). The discovery of sex influenced , sex
limited and sex linked hereditary .
 Joron M, Papa R, Beltran M, et al (2006). A conserved supergene
locus controls colour patterns diversity in Heliconius Butterfly.
 www.sciencehub.com
 www.ilamkidunya.com
Sex linkage

Sex linkage

  • 2.
  • 3.
  • 4.
     SEX LINKAGE HISTORY  TYPES OF SEX LINKAGE  SEX LINKAGE IN HUMAN  COLOUR BLINDNESS  CAUSES OF COLOUR BLINDNESS  TYPE OF COLOUR BLINDNESS  EXAPLE OD COLOUR BLINDNESS  TEST CROSS  SYPTOMS  DETECTION  EFFECTS  SEX INFLUENCED TRAIT  SEX LIMITED TRAIT  CONCLUSION
  • 5.
    DEFINITION: Sex linkage isthe phenotypic expression of an allele that is independent on he gender of the individual and is directly tied to sex chromosome. HISTORY: THOMAS MORGAN: Sex linkage was first discovered by Thomas Morgan in 1910 who observed a disproportionate percentage of white- eye male fruits flies. This experiment involved crossing purebred red-eyed female fruit flies with these mutant white – eyed males. The result was exclusively red – eyed individuals of both sexes.
  • 7.
    There are someexamples of sex linkage. 1. Hemophilia 2. Red- green colour blindness 3. Congenital night blind ness 4. Some high blood pressure genes 5. Fragile X syndrome
  • 8.
  • 9.
     Twenty genesare sex linked.  Red green colour blindness and hemophilia  Both these disease are sex linked recessive trait.
  • 10.
     DEFINITION Colour blindnessis a condition in which individuals have difficulty in distinguishing red from green.
  • 12.
     Cats andDogs To see in full colour as we know it, humans use three cones red, blue, and green. However cats and dogs have only blue and green cones. This means they have much more muted perception of colour, which akin to colour blindness in humans.
  • 13.
     There arethree types of colour blindness.  Protanolay:  It is a type of o colour blind ness which reduce to red colour.  Deuteranomaly Which reduce sensitivity to green color. Tritanomaly Which reduce sensitivity to blue colour.
  • 14.
     E.B Wilsonfirstly discovered facts about hereditary color blindness  It is genetic disease and inherited from mother to child  Gene for colour blindness present on X chromosome  Colour blindness occurs in about 8% males and only 0.5% in females  Some people become colour blind due to other disease like diabetes and medication and multiple sclerosis.
  • 15.
     Why blindnesscolour is occur more in males instead of females.  Father transfer his x chromosomes to all daughter and mother transfer her x chromosome.  Son will be colour blind and daughter will be normal if his mother is carrier father is normal  Colour blind daughter will be produce only produce only when his father is colour blind and mother is carrier or colour blind.  Since such marriages are very rare.
  • 16.
     If motheris normal father is colour blind  Then son will be normal and daughter will be carrier.
  • 18.
    TEST CROSS-2 If motheris carrier and father is colour blind. 50 percent chances daughter may be colour blind or carrier. 50 percent chances son will be normal or colour blind.
  • 19.
    TEST CROSS -3 Ifmother is colour blind and father is normal. All sons will be colour blind and all daughter will be carriers.
  • 20.
     Symptoms ofcolour blindness could range from mild to severe.  Example would be difficult distinguishing between colors, or inability to see shades of the same color.  Rapid eye movement could occur in rare cases, and sensitivity of bright light.  They could also suffer from having trouble seeing the brightness of color in the usual way.  Inability to tell the difference between the shades of same or similar colors.  Particularly red and green or blue or yellow.
  • 21.
     It canbe detected by using special charts made up of coloured dots  These dots are so arranged that coloured blind person can see a different patterns  Sex linked traits in other animals:  White eyes in drosophila melanogaster flies – the first sex linked gene discovered.  Fur colour in domestic cats : the gene that causes orange pigment is on the X chromosome; thus a calico or tortoiseshell cat, with both black and orange pigment, is nearly always female.  The first sex- linked gene ever discovered was the lacticolor X linked recessive gene in the moth.
  • 22.
     Sex –influenced traits :  Sex influenced or sex conditioned traits are phenotypes affected by whether they appear in a male or female body. Even in a homozygous dominant or recessive female the condition may not be expressed fully.  Example : The baldness in humans.  Sex limited traits: These are characters only expressed in one sex. They may be caused by gene on either autosomal or sex chromosome
  • 23.
  • 24.
     There areno treatments for most types of color vision difficulties, unless the colour vision problem is related to the use of certain medicine or eye condition.  Discontinuing the medication causing your vision problem or treating the underlying eye disease may result in better color vision.
  • 25.
     Morgan’s conclusionwas the trait for eye color must be encoded on the X chromosome, and that white eyes must represent the recessive allele.
  • 26.
     References:  Morgan,Thomas 1919. The physical basis of hereditary  Genetics home reference (2006), genetic condition illustration, national library of medicine  Don caster L.& Raynor G.H 1906. Breeding experiments with Lepidoptera. Proceeding of the zoological society of London.  Ford E.B (1965) Genetics polymorphism. p17 – 25.MIT Press1965.  Mallet J. Joron M. (1999) the evolution diversity in warning color and mimicry polymorphisms, shifting balance, and speciation.  Zirkle, Conway (1946). The discovery of sex influenced , sex limited and sex linked hereditary .  Joron M, Papa R, Beltran M, et al (2006). A conserved supergene locus controls colour patterns diversity in Heliconius Butterfly.  www.sciencehub.com  www.ilamkidunya.com