NEET Exam  >  NEET Notes  >  Additional Study Material for NEET  >  Sex Linked Inheritance: Colour Blindness & others

Sex Linked Inheritance: Colour Blindness & others | Additional Study Material for NEET PDF Download

SEX LINKAGE

Sex Linked Inheritance: Colour Blindness & others | Additional Study Material for NEET

When the genes are present on sex-chromosome is termed as sex linked gene and such phenomenon is known as sex-linkage. Two - types of sex linkage :

1. X-linkage.
Genes of somatic characters are found on x-chromosome. The inheritance of x-linked character may be through the males and females. e.g. Haemophilia, Colour blindness

2. Y- linkage - The genes of somatic characters are located on Y- chromosome. The inheritance of such type of character is only through the males. Such type of character is called Holandric character. These characters
found only in male.

e.g. (1) Gene which forms TDF /sry-gene                   
(3) Webbed toes
(2) Hypertrichosis (excessive hair on ear pinna.)       
(4) Porcupine skin

Gene which is located on differential region of Y - chromosome is known as Holandric gene.

Example of X-Sex linkage :-
 

[i] Eye colour in Drosophila :- Eye colour in Drosophila is controlled by a X–linked gene.

If a red eyed colour gene is represented as '+' and white eyed colour represented as 'w', then on basis of this different type of genotypes are found in Drosophila.

Gene for red eye is dominant (+) and white colour of eye is recessive (w)

Homozygous red eyed female = X+X+
Heterozygous red eyed female = X+Xw
Homozygous white eyed female = XwXw
Hemizygous red eyed male = X+Y
Hemizygous white eyed male = XwY

It is clear by above different types of genotype that female either homozygous or heterozygous for eye colour. But, for the male eye colour, it is always hemizygous.

[ii] Haemophilia :-

Haemophilia is also called "bleeder's disease" and first discovered by John Otto (1803). The gene of haemophilia is recessive and x-linked lethal gene.

On the basis of x-linked, following types of genotype are found.

Xh X = Carrier female
XhXh = Affected female
XhY = Affected male.

But, XhXh type of female dies during embryo stage because in homozygous condition, this gene becomes lethal and causes death.

Haemophilia -A → due to lack of factor -VIII (Anti-haemophilic globulin AHG)

Haemophilia B or Christmas disease - due to lack of factor - IX (Plasma thromboplastin component)

Haemophilia - C (Antosomal disorder) → due to lack of factor - XI (Plasma Thromboplastin antecedent)

[iii] Colour Blindness :- The inheritance of colour-blindness is alike as haemophilia, but it is not a lethal disease so it is found in male and female.(discovered by Horner)

Three types of colour blindness are-
 [a] Protanopia 
:- It is for red colour.
[b] Deuteranopia :- It is for green colour
[c] Tritanopia :- For blue colour blindness. Colour blindness is checked by ishihara - chart.

Other examples of X - sex linkage
[iv] Diabetes insipidus (recessive).
[v] Duchenne muscular dystrophy (recessive).
[vi] Fragile xsyndrome(recessive).
[vii] Pesudoricketes (Dominant)
[viii] Defective enamel of teeth (Dominant)

Examples of X-Y linkage
(i) Xeroderma pigmentosum
(ii) Epidermolysis bullosa 

Types of Inheritance of sex linked characters :-
 1. Criss cross inheritance (Morgan)
:- In criss-cross inheritance male or female parent transfer a X- linked character to grandson or grand daughter through the offspring of opposite sex.

(a) Diagenic (Diagynic) :- Inheritance in which characters are inherited from father to the daughter and from daughter to grandson.

Father → daughter → grand son.

(b) Diandric :- Inheritance in which characters are inherited from mother to the son and from son to grand daughter.

Mother → Son → Grand-daughter.

(2) Non criss-cross inheritance : In this inheritance male or female parent transfer sex linked character to grand son or grand daughter through the offspring of same sex.
(a) Hologenic (Hologynic) :- Mother → Daughter → Grand-daughter (female to female)
(b) Holandric :- Father → Son → Grand-son (male to male)

Sex-Limited Character :- These characters are present in one sex and absent in another sex. But their genes are present in both the sexes and their expression is depend on sex hormone.

Example :- Secondary sexual characters → these genes located on the autosomes and these genes are present in both male and female, but effect of these are depend upon presence or absence of sex-hormones.

For example - genes of beard-moustache express their effects only in the presence of male hormone - testosterone.

Sex Influenced Characters : - Genes of these characters are also present on autosomes but they are influenced differently in male and female. In heterozygous condition their effect is different in both the sexes.

Example :- Baldness :- Gene of baldness is dominant (B).

Genotype

Male

Female

BB

Baldness present

Baldness present

bb

Baldness absent

Baldness absent

Bb

Baldness present

Baldness absent

Gene Bb shows partiality in male and female, Baldness is found in male due to effect of this gene, but baldness is absent in female with this genotype.

The document Sex Linked Inheritance: Colour Blindness & others | Additional Study Material for NEET is a part of the NEET Course Additional Study Material for NEET.
All you need of NEET at this link: NEET
26 videos|287 docs|64 tests

Top Courses for NEET

FAQs on Sex Linked Inheritance: Colour Blindness & others - Additional Study Material for NEET

1. What is sex-linked inheritance?
Ans. Sex-linked inheritance refers to the inheritance of specific traits or disorders that are linked to the sex chromosomes (X and Y). This means that the presence or absence of these traits is determined by the genes located on the sex chromosomes.
2. What is color blindness?
Ans. Color blindness is a genetic condition that affects a person's ability to perceive certain colors. In most cases, it is caused by a mutation or defect in the genes that are responsible for the perception of color. People with color blindness may have difficulty distinguishing between certain colors, such as red and green.
3. How is color blindness inherited?
Ans. Color blindness is often inherited in a sex-linked manner, specifically through the X chromosome. The gene responsible for color vision is located on the X chromosome, and since males have only one X chromosome, they are more likely to inherit color blindness if their mother carries the affected gene.
4. Can females be color blind?
Ans. Yes, females can be color blind, but it is relatively rare. Since females have two X chromosomes, they have a higher chance of having one normal gene that compensates for any defective gene on the other X chromosome. Thus, for a female to be color blind, both of her X chromosomes must carry the defective gene.
5. What are some other examples of sex-linked disorders?
Ans. Apart from color blindness, other examples of sex-linked disorders include hemophilia, Duchenne muscular dystrophy, and certain types of intellectual disability. These disorders are more commonly observed in males due to the inheritance pattern of the X chromosome. Females can also be carriers of these disorders without showing symptoms.
26 videos|287 docs|64 tests
Download as PDF
Explore Courses for NEET exam

Top Courses for NEET

Signup for Free!
Signup to see your scores go up within 7 days! Learn & Practice with 1000+ FREE Notes, Videos & Tests.
10M+ students study on EduRev
Related Searches

Important questions

,

Summary

,

past year papers

,

Extra Questions

,

practice quizzes

,

Sex Linked Inheritance: Colour Blindness & others | Additional Study Material for NEET

,

study material

,

mock tests for examination

,

Viva Questions

,

shortcuts and tricks

,

pdf

,

Sex Linked Inheritance: Colour Blindness & others | Additional Study Material for NEET

,

MCQs

,

Semester Notes

,

ppt

,

Previous Year Questions with Solutions

,

Free

,

Exam

,

Objective type Questions

,

video lectures

,

Sex Linked Inheritance: Colour Blindness & others | Additional Study Material for NEET

,

Sample Paper

;