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Natural mutation and its primary sources, Study notes of Genetics

Natural mutation is a spontaneous alteration in the genetic material of an organism. It’s a fundamental mechanism of evolution, as it introduces new genetic variations. Here are the primary sources of natural mutations: DNA Replication Errors: During DNA replication, errors can occur, such as the mispairing of bases or the insertion or deletion of bases. These errors can lead to mutations if not corrected by the DNA repair machinery. Chemical Mutagens: Certain chemicals can interact with DNA and cause mutations. These include reactive oxygen species, alkylating agents, and base analogs.

Typology: Study notes

2023/2024

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13. Spontaneous or natural mutation and primary sources.
1. A mutation is a change in the DNA sequence of an
organism. Mutations can result from errors in DNA
replication during cell division, exposure to mutagens or a
viral infection.
2. Spontaneous mutations in DNA refer to changes in the
genetic sequence that occur naturally due to errors in
biological processors.
3. These mutations are not caused by an environmental factor
but occur during normal cellular processes.
4. Spontaneous mutation occurs naturally about 1 in every
million to 1 in every billion divisions and is probably due to
low level natural mitagens normally present in the
environment.
5. The primary sources of spontaneous mutations are:
1. Tautomerism:
1. Tautomerism is the relationship between two structural
isomers that are in chemical equilibrium and ready to
change into one another.
2. Generally the bases exist in keto form but at a time they can
take on either an imino or enol form.
3. Rare form of Adenine can pair with cytosine, and the end
form of thymine can pair with the guanine. These tautomeric
shifts alter the hydrogen bonding characteristics of the
bases and permits for pirine substitution or pyramidine for
pyramidine substitution.
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  1. Spontaneous or natural mutation and primary sources.
    1. A mutation is a change in the DNA sequence of an organism. Mutations can result from errors in DNA replication during cell division, exposure to mutagens or a viral infection.
    2. Spontaneous mutations in DNA refer to changes in the genetic sequence that occur naturally due to errors in biological processors.
    3. These mutations are not caused by an environmental factor but occur during normal cellular processes.
    4. Spontaneous mutation occurs naturally about 1 in every million to 1 in every billion divisions and is probably due to low level natural mitagens normally present in the environment.
    5. The primary sources of spontaneous mutations are:
      1. Tautomerism:
    6. Tautomerism is the relationship between two structural isomers that are in chemical equilibrium and ready to change into one another.
    7. Generally the bases exist in keto form but at a time they can take on either an imino or enol form.
    8. Rare form of Adenine can pair with cytosine, and the end form of thymine can pair with the guanine. These tautomeric shifts alter the hydrogen bonding characteristics of the bases and permits for pirine substitution or pyramidine for pyramidine substitution.
  1. Spontaneous deamination : ● Deamination is the loss of amino group from the bases. ● Both 5 methyl-cytosine and cytosine occasionally loose an amino group, resulting in cytosine converted to uracil and 5 methyl-cytosine to thymine. ● This results in cytosine pairing with adenine, but not with guanine, therefore, replication of molecule containing GU base pair will finally result in substitution of an AT pair for the original GC pair.
  2. Depurination: ● Depurination refers to the loss of a purine base from the DNA molecule. ● This occurs when the beta-N-glycosidic bond between the purine base and deoxyribose sugar in the DNA backbone is hydrolysed. ● When depurination occurs, it leaves behind an apurinic site, also known as AP site. If this site is not repaired before DNA replication, the DNA polymerase may insert an incorrect nucleotide opposite the AP site.

denaturation and displacement of the DNA strands, resulting in mispairing of the complementary bases.

  1. Unequal crossing over:

● It is a type of chromosomal crossover that occurs between homologous sequences that are not paired precisely. This can lead to gene duplication or deletion events. ● Repeated rounds of unequal crossing over causes the homogenization of the two sequences.