This document discusses sex linkage and color blindness. It begins by defining sex linkage as the phenotypic expression of an allele that is tied to an individual's sex chromosome. It then discusses Thomas Morgan's discovery of sex linkage in fruit flies in 1910. There are several examples of sex-linked traits provided, including hemophilia, color blindness, and fragile X syndrome. Color blindness is discussed in more detail, including its inheritance pattern and different types. Causes, symptoms, detection, and effects of color blindness are also outlined. The document concludes by restating Morgan's findings about the inheritance of eye color in fruit flies.
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.
Chromosomal Basis of Inheritance
Be familiar with patterns of inheritance for autosomal and sex linked genes
Understand the concept of “Linked Genes”
Understand how traits affected by incomplete dominance and codominance differ from autosomal dominant and autosomal recessive traits
Understand how nondisjunction of chromosomes can lead to disorders.
Linked genes: are those that reside on the same chromosome and tend to be inherited together
Humans have 23 pairs of chromosomes
Autosomal genes reside on the autosomal chromosomes (pairs 1-22)
Sex-linked genes are found on the sex chromosomes
(pair 23, usually on the X)
Autosomal genes are usually represented by a pair of alleles
The phenotype of the gene reflects the dominant or recessive relationship of the alleles.
Most autosomal genetic diseases are autosomal recessive meaning the individual need to be homozygous recessive to exhibit the condition
(example: cystic fibrosis) Production of abnormmaly thick mucus. Leading to the blockage of panreatic duct, intestines and respiratory infection.
Huntington’s disease is an autosomal dominant disorder meaning that is a single Huntingtons allele is inherited, the individual will have the disease.
Some alleles do not show a dominance hierarchy
Incomplete dominance: the phenotype of a heterozygous genotype is intermediate in appearance
Codominance: each allele in the genotype for a particular gene will be expressed in the phenotype
Males and females differ in their sex chromosome combination
(females XX; males XY)
Because the X contains genes and the Y “does not”, inheritance patterns of sex-linked genes vary between the sexes
recessive traits more prevalent in males
Genetic disorders can also occur due to errors in the number of inherited chromosomes
This condition arises through a problem that occurs during meiosis
Although female mammals, including humans, inherit two X chromosomes, one X chromosome in each cell becomes almost completely inactivated during embryonic development.
Barr body
Nondisjunction:
Leads to aneuploidy:
Aneuploidy: is the condition of having less than or more than the normal diploid number of chromosomes, and is the most frequently observed type of cytogenetic abnormality.
Mendelian inheritance has its physical basis in the behavior of chromosomes during sexual life cycles.
Morgan traced a gene to a specific chromosome.
Sex-linked genes have unique patterns of inheritance.
Alterations of chromosome numbers or structure cause some genetic disorders.
Linked genes tend to be inherited together because they are located on the same chromosome.
Independent assortment of chromosomes and crossing over produce genetic variation (recombinants)
Geneticists can use recombination data to map a chromosomes genetic loci.
Chromosomal basis for sex is dependent upon the organism.
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.
Chromosomal Basis of Inheritance
Be familiar with patterns of inheritance for autosomal and sex linked genes
Understand the concept of “Linked Genes”
Understand how traits affected by incomplete dominance and codominance differ from autosomal dominant and autosomal recessive traits
Understand how nondisjunction of chromosomes can lead to disorders.
Linked genes: are those that reside on the same chromosome and tend to be inherited together
Humans have 23 pairs of chromosomes
Autosomal genes reside on the autosomal chromosomes (pairs 1-22)
Sex-linked genes are found on the sex chromosomes
(pair 23, usually on the X)
Autosomal genes are usually represented by a pair of alleles
The phenotype of the gene reflects the dominant or recessive relationship of the alleles.
Most autosomal genetic diseases are autosomal recessive meaning the individual need to be homozygous recessive to exhibit the condition
(example: cystic fibrosis) Production of abnormmaly thick mucus. Leading to the blockage of panreatic duct, intestines and respiratory infection.
Huntington’s disease is an autosomal dominant disorder meaning that is a single Huntingtons allele is inherited, the individual will have the disease.
Some alleles do not show a dominance hierarchy
Incomplete dominance: the phenotype of a heterozygous genotype is intermediate in appearance
Codominance: each allele in the genotype for a particular gene will be expressed in the phenotype
Males and females differ in their sex chromosome combination
(females XX; males XY)
Because the X contains genes and the Y “does not”, inheritance patterns of sex-linked genes vary between the sexes
recessive traits more prevalent in males
Genetic disorders can also occur due to errors in the number of inherited chromosomes
This condition arises through a problem that occurs during meiosis
Although female mammals, including humans, inherit two X chromosomes, one X chromosome in each cell becomes almost completely inactivated during embryonic development.
Barr body
Nondisjunction:
Leads to aneuploidy:
Aneuploidy: is the condition of having less than or more than the normal diploid number of chromosomes, and is the most frequently observed type of cytogenetic abnormality.
Mendelian inheritance has its physical basis in the behavior of chromosomes during sexual life cycles.
Morgan traced a gene to a specific chromosome.
Sex-linked genes have unique patterns of inheritance.
Alterations of chromosome numbers or structure cause some genetic disorders.
Linked genes tend to be inherited together because they are located on the same chromosome.
Independent assortment of chromosomes and crossing over produce genetic variation (recombinants)
Geneticists can use recombination data to map a chromosomes genetic loci.
Chromosomal basis for sex is dependent upon the organism.
Lecture given by Leon MUTESA, MD,PhD , a genetician teaching at UR( UNIVERSITY OF RWANDA, HUYE CAMPUS,SCHOOL OF MEDICINE AND PHARMACY, DEPARTMENT OF GENERAL MEDICINE AND SURGERY).
Chapter 15: Chromosomal Basis of InheritanceAngel Vega
KEY CONCEPTS
15.1 Morgan showed that Mendelian inheritance has its physical
basis in the behavior of chromosomes: Scientific inquiry
15.2 Sex-linked genes exhibit unique patterns of inheritance
15.3 Linked genes tend to be inherited together because they are located near each other on the same chromosome
15.4 Alterations of chromosome number or structure cause
some genetic disorders
15.5 Some inheritance patterns are exceptions to standard
Mendelian inheritance
This presentation intends to explore the sex-linked characters along with some fatal diseases of human beings, their cause, consequences and other issues.
Lecture given by Leon MUTESA, MD,PhD , a genetician teaching at UR( UNIVERSITY OF RWANDA, HUYE CAMPUS,SCHOOL OF MEDICINE AND PHARMACY, DEPARTMENT OF GENERAL MEDICINE AND SURGERY).
Chapter 15: Chromosomal Basis of InheritanceAngel Vega
KEY CONCEPTS
15.1 Morgan showed that Mendelian inheritance has its physical
basis in the behavior of chromosomes: Scientific inquiry
15.2 Sex-linked genes exhibit unique patterns of inheritance
15.3 Linked genes tend to be inherited together because they are located near each other on the same chromosome
15.4 Alterations of chromosome number or structure cause
some genetic disorders
15.5 Some inheritance patterns are exceptions to standard
Mendelian inheritance
This presentation intends to explore the sex-linked characters along with some fatal diseases of human beings, their cause, consequences and other issues.
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I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
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I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
I AM HAFIZ MUHAMMAD WASEEM from mailsi vehari
BSc from science college Multan
MSC university of education Lahore
i love Pakistan and my teachers and my parents
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This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
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 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.
6.
7. 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
12. 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.
13. 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.
14. 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.
15. 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.
16. If mother is normal father is colour blind
Then son will be normal and daughter will be
carrier.
17.
18. 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.
19. TEST CROSS -3
If mother is colour
blind and father is
normal.
All sons will be
colour blind and all
daughter will be
carriers.
20. 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.
21. 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.
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
24. 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.
25. 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.
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.
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