LINKAGE AND CROSSING OVER
• SUBMITTED BY : MUHAMMAD BILAL
• SUBMITTED TO:DR WAQAS AHMAD
• (UNIVERSITY OF SARGODHA)
Genetic linkage
•Genetic linkage is the tendency of alleles that are
located close together on a chromosome to be
inherited together during meiosis.
•Genes whose loci are nearer to each other are less
likely to be separated on to different chromatids
during chromosomal crossover, and are therefore
said to be genetically linked.
Linked Genes
•Independent assortment states that during
gamete formation, the two alleles for one
gene segregate or assort independently of
the alleles for other genes.
•But if two genes are found on the same
chromosome, they will not assort
independently, and do not follow
Mendelian inheritance patterns.
•Genes that are inherited together are said to
be “linked.”
•Genes located on different chromosomes are not linked
This allows independent assortment – in a di-hybrid cross
the traits show the classic 9:3:3:1 inheritance pattern.
• Genes that are located very close together on the same
chromosome may show complete linkage.
•They may be so close to each other that they cannot be
separated by recombination during meiosis.
(c) Genes located far apart on the same
chromosome typically show incomplete
(partial) linkage because they are easily
separated by recombination.
The discovery of genetic linkage
•William Bateson and Reginald Punnett
completed a study in 1905 that determined the
movement of alleles found on the same
chromosome.
•The study used sweet peas, particularly flower
colour and pollen shape, they followed the
inheritance pattern.
 William
Bateson
 Reginald
Punnett
• For flower colour, purple is dominant over
red, and for pollen shape long is dominant
over round.
• A cross was performed using a true
breeding purple/long and red/round.
• The F1 generation was 100% purple/long.
•Crossing two individuals from the F1 generation resulted
in a F2 generation with four different phenotypes.
(purple/long, purple/round, red/long and red/round).
•The alleles that created these combinations did not
follow the 9:3:3:1 pattern, but supported the idea that
these alleles did not assort independently and therefore
must be linked.
Why Linkage?
•Linkage refers to packaging genes onto
chromosomes.
•Chromosomes (and therefore linkage) are for
organizing genes for their safe coordinated
transmission from cell to cell( parent to offspring).
Types of Linkage
•Depending upon the presence or absence of
new combinations or non-parental
combinations, linkage can be of two types:
1.Complete linkage
2.Incomplete linkage
1.Complete linkage
•If two or more characters are inherited together and
consistently appear in two or more generations in
their original or parental combinations, it is called
complete linkage.
•Genes showing complete linkage are closely
located in the same chromosome.
2.Incomplete linkage
•Incomplete linkage is exhibited by those
genes which produce some percentage of
non-parental combinations. Such genes are
located distantly on the chromosome
Complete vs. Incomplete Linkage
Significance of linkage
1.Linkage does not permit the breeders to bring
the desirable characters in one variety.
2. Linkage reduces the chance of recombination
of genes and thus helps to hold parental
characteristics together.
Crossing Over
Crossing Over
•It is a basic concept of genetics and cell biology, often
called recombination.
• The term crossing over was coined by Morgan.
•It is the exchange of genes between two chromosomes,
resulting in non-identical chromatids that comprise the
genetic material of gametes.
Occurrence
• This process occurs during Prophase I of Meiosis, just
prior to chromosome alignment and splitting of the
cell.
• As an exception , it can also occur in MITOSIS which
may result in heterozygosity. But the frequency of
crossing over is much higher in meiosis.
• Cross over events happen approximately 57 times in
males and around 75 times in females.
Mechanism of crossing over
• Crossing over, leading to recombination of linked
genes, is due to interchange of sections of
homologous chromosomes.
• At meiosis, the homologous chromosomes come
together and pair, or synapse, during prophase.
• The pairing is remarkably precise and is evidently
brought about by mutual attraction of the parts of the
chromosomes that are similar or homologous because
they contain allellic genes.
The enzymes involved in crossing over
• 1) Recombinase is the major enzyme regulating
recombination event
• 2) Endonuclease
• 3) Ligase enzyme
• Endonuclease is responsible for breakage of 2 non-
sister chromatids at corresponding sites. This is
followed by the exchange of segments and finally the
exchanged segments are joined or the gap is filled by
ligase enzyme.
• The final step is terminalisation. After crossing
over the non-sister chromatids starts to repel
each other and desynapsis takes place.
• Chiasma moves in a zipper fashion towards the
end of tetrad. This movement of chiasma is
known as terminalisation.
• As a result of terminalisation, homologous
chromosomes are separated completely.
Recombination Frequency
• Recombination frequency (θ) is the frequency with which a
single chromosomal crossover will take place between two
genes during meiosis.
• The recombination frequency will be 50% when two genes
are located on different chromosomes or when they
are widely separated on the same chromosome.
• This is a consequence of independent assortment. When two
genes are close together on the same chromosome, they do
not assort independently and are said to be linked.
FACTORS AFFECTING CROSS OVER
1. Sex
2. Mutation
3. Age
4. X-Ray effect
5. Temperature
6. Distance between genes
7. Decreased Hydration
8. Chemicals
1. Sex:
There is a tendency of reduction of crossing over in male
mammals.
2. Mutation:
Mutation reduces crossing over.
3. Age:
Older age increases the rate of crossing over
4. Distance between the genes:
This is perhaps the most important factor influencing the frequency
of cross over between two gene loci. As has been repeatedly
pointed out
5. X-ray Effect:
X-ray radiations increase crossing over near centromere.
6.Temperature:
High and low temperature variations increase the percentage of
crossing over in certain parts of the chromosome.
7.Decreased Hydration:
Lowering of water content in the surroundings is known to reduce the
frequency of chiasma. It may even result in complete suppression of
cross over in extreme dehydrated conditions (Sybenga 1972).
8. Chemicals:
Certain chemicals which induce chromosomal aberrations are also
known to induce or suppress crossing over. Ethyl methane sulphonate
is known to induce somatic cross over. Colchicine also prevents cross
over by preventing pairing between chromosomes.
Significance of Crossing-over
1.Produces new combinations of traits.
2.Through crossing over segments of
homologous chromosomes are
interchanged.
3.Crossing over plays a very important role in
the field of breeding to improve the varieties
of plants and animals.
Types of Crossing Over
i. Single Crossing Over
In this type of crossing over only one
chiasma is formed all along the length of
a chromosome pair. Gametes formed by
this type of crossing over are called
single cross over gametes .
(ii) Double Crossing Over:
In this type two chiasmata are formed along the
entire length of the chromosome leading to
breakage and rejoin of chromatids at two points.
(iii) Multiple Crossing Over:
In this type more than two chiasmata are formed
and thus crossing over occurs at more than two
points on the same chromosome pair.
Difference between linkage and Crossing Over
Crossing Over
• It leads to separation of
linked genes.
• It involves Non sister
chromatids of homologous
chromosomes.
• It increase variability by
forming new gene
combinations.
Linkage
• It keeps the genes
together.
• It involves individual
chromosomes.
• It reduces variability.
LINKAGE AND CROSSING OVER

LINKAGE AND CROSSING OVER

  • 2.
    LINKAGE AND CROSSINGOVER • SUBMITTED BY : MUHAMMAD BILAL • SUBMITTED TO:DR WAQAS AHMAD • (UNIVERSITY OF SARGODHA)
  • 3.
    Genetic linkage •Genetic linkageis the tendency of alleles that are located close together on a chromosome to be inherited together during meiosis. •Genes whose loci are nearer to each other are less likely to be separated on to different chromatids during chromosomal crossover, and are therefore said to be genetically linked.
  • 4.
    Linked Genes •Independent assortmentstates that during gamete formation, the two alleles for one gene segregate or assort independently of the alleles for other genes.
  • 5.
    •But if twogenes are found on the same chromosome, they will not assort independently, and do not follow Mendelian inheritance patterns. •Genes that are inherited together are said to be “linked.”
  • 7.
    •Genes located ondifferent chromosomes are not linked This allows independent assortment – in a di-hybrid cross the traits show the classic 9:3:3:1 inheritance pattern. • Genes that are located very close together on the same chromosome may show complete linkage. •They may be so close to each other that they cannot be separated by recombination during meiosis.
  • 8.
    (c) Genes locatedfar apart on the same chromosome typically show incomplete (partial) linkage because they are easily separated by recombination.
  • 9.
    The discovery ofgenetic linkage •William Bateson and Reginald Punnett completed a study in 1905 that determined the movement of alleles found on the same chromosome. •The study used sweet peas, particularly flower colour and pollen shape, they followed the inheritance pattern.
  • 10.
  • 11.
    • For flowercolour, purple is dominant over red, and for pollen shape long is dominant over round. • A cross was performed using a true breeding purple/long and red/round. • The F1 generation was 100% purple/long.
  • 12.
    •Crossing two individualsfrom the F1 generation resulted in a F2 generation with four different phenotypes. (purple/long, purple/round, red/long and red/round). •The alleles that created these combinations did not follow the 9:3:3:1 pattern, but supported the idea that these alleles did not assort independently and therefore must be linked.
  • 14.
    Why Linkage? •Linkage refersto packaging genes onto chromosomes. •Chromosomes (and therefore linkage) are for organizing genes for their safe coordinated transmission from cell to cell( parent to offspring).
  • 15.
    Types of Linkage •Dependingupon the presence or absence of new combinations or non-parental combinations, linkage can be of two types: 1.Complete linkage 2.Incomplete linkage
  • 16.
    1.Complete linkage •If twoor more characters are inherited together and consistently appear in two or more generations in their original or parental combinations, it is called complete linkage. •Genes showing complete linkage are closely located in the same chromosome.
  • 17.
    2.Incomplete linkage •Incomplete linkageis exhibited by those genes which produce some percentage of non-parental combinations. Such genes are located distantly on the chromosome
  • 18.
  • 19.
    Significance of linkage 1.Linkagedoes not permit the breeders to bring the desirable characters in one variety. 2. Linkage reduces the chance of recombination of genes and thus helps to hold parental characteristics together.
  • 20.
  • 21.
    Crossing Over •It isa basic concept of genetics and cell biology, often called recombination. • The term crossing over was coined by Morgan. •It is the exchange of genes between two chromosomes, resulting in non-identical chromatids that comprise the genetic material of gametes.
  • 22.
    Occurrence • This processoccurs during Prophase I of Meiosis, just prior to chromosome alignment and splitting of the cell. • As an exception , it can also occur in MITOSIS which may result in heterozygosity. But the frequency of crossing over is much higher in meiosis. • Cross over events happen approximately 57 times in males and around 75 times in females.
  • 23.
    Mechanism of crossingover • Crossing over, leading to recombination of linked genes, is due to interchange of sections of homologous chromosomes. • At meiosis, the homologous chromosomes come together and pair, or synapse, during prophase. • The pairing is remarkably precise and is evidently brought about by mutual attraction of the parts of the chromosomes that are similar or homologous because they contain allellic genes.
  • 25.
    The enzymes involvedin crossing over • 1) Recombinase is the major enzyme regulating recombination event • 2) Endonuclease • 3) Ligase enzyme • Endonuclease is responsible for breakage of 2 non- sister chromatids at corresponding sites. This is followed by the exchange of segments and finally the exchanged segments are joined or the gap is filled by ligase enzyme.
  • 26.
    • The finalstep is terminalisation. After crossing over the non-sister chromatids starts to repel each other and desynapsis takes place. • Chiasma moves in a zipper fashion towards the end of tetrad. This movement of chiasma is known as terminalisation. • As a result of terminalisation, homologous chromosomes are separated completely.
  • 27.
    Recombination Frequency • Recombinationfrequency (θ) is the frequency with which a single chromosomal crossover will take place between two genes during meiosis. • The recombination frequency will be 50% when two genes are located on different chromosomes or when they are widely separated on the same chromosome. • This is a consequence of independent assortment. When two genes are close together on the same chromosome, they do not assort independently and are said to be linked.
  • 29.
    FACTORS AFFECTING CROSSOVER 1. Sex 2. Mutation 3. Age 4. X-Ray effect 5. Temperature 6. Distance between genes 7. Decreased Hydration 8. Chemicals
  • 30.
    1. Sex: There isa tendency of reduction of crossing over in male mammals. 2. Mutation: Mutation reduces crossing over. 3. Age: Older age increases the rate of crossing over 4. Distance between the genes: This is perhaps the most important factor influencing the frequency of cross over between two gene loci. As has been repeatedly pointed out
  • 31.
    5. X-ray Effect: X-rayradiations increase crossing over near centromere. 6.Temperature: High and low temperature variations increase the percentage of crossing over in certain parts of the chromosome. 7.Decreased Hydration: Lowering of water content in the surroundings is known to reduce the frequency of chiasma. It may even result in complete suppression of cross over in extreme dehydrated conditions (Sybenga 1972). 8. Chemicals: Certain chemicals which induce chromosomal aberrations are also known to induce or suppress crossing over. Ethyl methane sulphonate is known to induce somatic cross over. Colchicine also prevents cross over by preventing pairing between chromosomes.
  • 32.
    Significance of Crossing-over 1.Producesnew combinations of traits. 2.Through crossing over segments of homologous chromosomes are interchanged. 3.Crossing over plays a very important role in the field of breeding to improve the varieties of plants and animals.
  • 33.
    Types of CrossingOver i. Single Crossing Over In this type of crossing over only one chiasma is formed all along the length of a chromosome pair. Gametes formed by this type of crossing over are called single cross over gametes .
  • 34.
    (ii) Double CrossingOver: In this type two chiasmata are formed along the entire length of the chromosome leading to breakage and rejoin of chromatids at two points. (iii) Multiple Crossing Over: In this type more than two chiasmata are formed and thus crossing over occurs at more than two points on the same chromosome pair.
  • 35.
    Difference between linkageand Crossing Over Crossing Over • It leads to separation of linked genes. • It involves Non sister chromatids of homologous chromosomes. • It increase variability by forming new gene combinations. Linkage • It keeps the genes together. • It involves individual chromosomes. • It reduces variability.