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Mailings Review View ferences av A. A AaBbCcDdEe 211 av AalbCcDdte AaBbCcD AaBbCcDdE AaB No Spacing Heading 1 Heading 2 Title
. A UN Normal No Spacing Heading 1 DAS 21.) Original template strand: 3 TAC GCA AGC AAT ACC GAC GAA S Mutation Describe wha
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2. In both prokaryotes and eukaryotes, genes are controlled by various factors and chemicals.

In both, genes are not active always. the genes are switched on and off to control the expression of the genes.

The difference between pro and eukaryotic genes regulation are---

In prokaryotes, genes are arranged in to operons and regulated. Where as in Eukaryotes, genes present on DNA are coiled around histone proteins. They are regulated by methylation, acetylation etc.

In prokaryotes, both transcription and translation occurs in the cytoplasm and regulation occurs in transcriptional level. Where as in eukaryotes, transcription occurs in nucleus and translation occurs in cytoplasm. Regulation occurs in transcriptional level and also translational level.

3. Advantage of alternate splicing is one mRNA can be used to produce different proteins by splicing different introns and keeping different exons.

4. Mutations---

Substitution of T for G at position 8:

3' TAC GCA ATC AAT ACC GAC GAA 5'

Here a pyramidine is replaced by purine. It is a point mutation and Transversion mutation. The mutation leads to change in amino acid from Serine to Stop codon.

Addition of T between 8 and 9.

3' TAC GCA AGT CAA TAC CGA CGA A 5'

Because of the addition, frame shift mutation occurs.

Aminoacid sequence changed from the region of addition to --Ser, Val, met, Ala, Ala.

Substitution of A for C at 15.

3' TAC GCA AGC AAT ACA GAC GAA 5'

Substitution of adenine in place of cytosine will result in change of amino acid from Trp to Cytosine. The mutation is transversion mutation.

Substitution of T for C at 18th position:

TAC GCA AGC AAT ACC GAT GAA

Substitution mutation is transition. Because a pyramidine is replaced by another pyramidine. There is no change in the amino acid coded in this mutation because of the degeneracy of the codon. Many codons code one amino acid.

Deletion of the C at position 18.

3' TAC GCA AGC AAT ACC GAG AA

This is deletion mutation. There is no change in he amino acid coded by the 6th codon. But 7th codon is of only 2 nucleotides, so no amino acid is coded by 7th codon. The polypeptide is shorter than normal.

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