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Chromosomal-Basis-Inheritance-Linkage-Crossing-over | uksir-notes | Genetics-5

Chromosomal Basis of Inheritance:


- After the re discovery of Mendel’s work, Sutton and Boveri started observing the behavior of Chromosomes.
Chromosome



Want to know about Deviation from Mendel's work , Click the link below:

https://uksirnotes.blogspot.com/2021/07/Genetics-Deviation-Mendelian-Inheritance-uksir.html

Want to know about History of Genetics and Mendel , Click the link below:

- Chromosomal basis of inheritance was proposed by Waler S. Sutton and Theodor Boveri. (1902)
- This theory states that chromosomes are the vehicles genetic hereditary units or genes.
- During gamete formation and fertilization, both the scientists observed a close parallelism between The mandelian factor and chromosome behavior.
- So they independently put forwarded the theory in 1902.

Parallelism between Chromosome and Mendelian Factors:

chromosome-gene
Chromosome and gene





Theory:

-       Every diploid organism performs Meiosis and fertilization during reproduction.

-       The chromosomal basis of inheritance proves that, Chromosomes are bearer of hereditary units or factors or genes.

-       Also each pair of mendelian factors is carried by a pair of chromosome separately.

-       Thus the mendelian factors or genes have specific loci on chromosomes (site where they exist)

-       The two alternative form of the gene found in two homologous chromosomes (at the same loci of both chromosome ) 




Chromosome

Chromosomal transfer



Linkage :

·    There must be independent assortment during the gamete formation, according to Mendel.

·    But sometime pairs of traits /characters are coupled and do not show independent assortment. (Do not separate generation after generation)

·    Thus the genes responsible for such characters are present in some chromosome and said to be linked.

·    This phenomenon of remaining together without separation of linked genes is called as linkage.

·    The linked genes of a chromosome form the linkage group.

·    Linkage was demonstrated by T.H. Morgan in 1910.

·    He performed a test cross in Drosophila (fruit fly) and got the result, described below.

 

Test Cross

 

Heterozygous                                  x               Homozygous recessive

(Grey body & long winged)                         (Black body & vestigial winged)

(Gg Ww)                                                              (ggww)

 

                         4 Type of phenotype found:

 

1.  Gray body long winged (GW)       – 41.5%

2.  Gray  body vestigial winged (Gw)                 - 8.5%

3.  Black body long winged (gW)        - 8.5%

4.  Black body vestigial winged (gw) - 41.5%

 

·    But, The result of Test cross must be 1 : 1 : 1 : 1 (i.e. 25% of every phenotype) according to Mendel.

·    It clearly indicates that, there are some traits (gene) do not want to separate from each other, generation after generation.

·    They have strong affinities and show linkage.

·    Here gray body trait is linked to long winged, likewise black body linked to vestigial wing.

Here two type of linkage can be found

(A) Complete linkage :

·    If both the gene for the traits present on the same pair of chromosome (Homologous chromosome), then there will be formation of only two type of phenotype :

                          Gray long       &       black vestigial (1 :1)

        Cross:

Complete Linkage












·    Here the change is 50% to both the phenotype.

·    These will not be any recombination.

·    So theoretically the result will be 1:1

(B) Incomplete linkage :

·    If both the dominant gene for the traits are on different homologous chromosome. Then there is more chances of separation.

·    In this case the theoretical ratio of phenotype will be  1 : 1 : 1 : 1.

·    As the gene can separate, there will be formation of 4 type of phenotype.

We can illustrate using alphabets :

(Example incomplete linkage)

                           Gary body long wing                             Black body vestigial wing

Incomplete Linkage

Crossing Over:

·    The deviation from linkage result in crossing over.

·    During meiosis homologous chromosome undergo a process called synapsis & after that exchange of chromosome fragments occurs. (Chiasma formation)

·    Here the alleles of the traits (genes) are exchanged, which is called as crossing over.

·    Due to this- two type of gametes are produced, one is parental type and other is recombinant type.

·    The recombinant type of gametes fuse to produce new variety of offspring (new trait)

Mechanism :


Crossing-over
Crossing-over

Crossing over



·    The two parental combination – have approximately equal proportion, likewise the two recombinant also have the same.

·    This result can be seen in through Morgan’s experiment.

 

 

Morgan Exp : 

Morgan Experiment


Generally recombinant types are produced in different proportion, depending on the linkage distance between the genes.

 

Recombination Frequency:

·    If complete linkage do not occur, then there will be formation of recombinants.

·    The frequency for occurrence of recombinant, is called as Recombination frequency or Crossover Frequency or Cross over Value.

·    The rate of crossing over is directly proportional to the distance between two gene.

·    That means if the Genes are more apart, hen more will be recombination frequency.

·    If genes are less apart, recombination frequency will be less.

Example :
Linkage-Map




Here the genes are arranged in linearly.

-       A and B genes are linked together, so there is less recombination frequency between them.

-       Whereas Between A and E there is maximum chance of recombination.

 

Formula for calculation of recombination frequency :

·    Recombination frequency =

Formula

·    Calculation of recombination frequency for linked genes help, to know the genetic linkage map in a chromosome.

·    Genetic linkage map is nothing but a map showing relative position of genes on a chromosome.

·    The distance between genes in gene map/linkage map is expressed as map unit/morgan unit (cM)

 

Example:



·    If recombination frequency between A & B is 6 cm, B & C is 7 cm x A& C is 13 cm, Then the gene loci/Locus will be :

Gene Loci



Want to know about Deviation from Mendel's work , Click the link below:

https://uksirnotes.blogspot.com/2021/07/Genetics-Deviation-Mendelian-Inheritance-uksir.html

Want to know about History of Genetics and Mendel , Click the link below:

Want to know about Mendel's Law of Inheritance, Click the link below:



This was all about Chromosomal Basis of Inheritance, Linkage and crossing over. Thanks for visiting, feel free to ask doubts in comment section... UK Sir


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