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Match the changed nucleotide sequences to the mutations that cause them.

Changed Nucleotide Sequences:
1. CATTCACACA
2. CATTCACACCACG
3. CATTTCACACG
4. CATTCACG
5. CATTECACAC

\begin{tabular}{|c|l|l|}
\hline
\textbf{Type of Mutation} & \textbf{Original Nucleotide Sequence} & \textbf{Changed Nucleotide Sequence} \\
\hline
Deletion & CATTCACACG & \\
\hline
Insertion & CATTCACACG & \\
\hline
Inversion & CATTCACACG & \\
\hline
Duplication & CATTCACACG & \\
\hline
Substitution & CATTCACACG & \\
\hline
\end{tabular}


Sagot :

Let's start by matching each changed nucleotide sequence to its corresponding type of mutation. The original nucleotide sequence is "CATTCACACG". The sequences that we're investigating are:
1. CATTCACACA
2. CATTCACACCACG
3. CATTTCACACG
4. CATTCACG
5. CATTECACAC

We are looking for specific types of mutations: deletion, insertion, inversion, duplication, and substitution.

1. CATTCACACA

This sequence is shorter than the original by one nucleotide. This indicates a deletion mutation. Therefore:
[tex]\[ \text{deletion} \quad \text{CATTCACACG} \quad \rightarrow \quad \text{CATTCACACA} \][/tex]

2. CATTCACACCACG

This sequence is longer than the original, and it appears that additional nucleotides have been inserted. This indicates an insertion mutation. Therefore:
[tex]\[ \text{insertion} \quad \text{CATTCACACG} \quad \rightarrow \quad \text{CATTCACACCACG} \][/tex]

3. CATTTCACACG

This sequence has the same length as the original but has one nucleotide difference (A instead of T in the 4th position). This signifies a substitution mutation. Therefore:
[tex]\[ \text{substitution} \quad \text{CATTCACACG} \quad \rightarrow \quad \text{CATTTCACACG} \][/tex]

4. CATTCACG

This sequence is shorter than the original, missing several nucleotides. This indicates another deletion mutation. Therefore:
[tex]\[ \text{deletion} \quad \text{CATTCACACG} \quad \rightarrow \quad \text{CATTCACG} \][/tex]

5. CATTECACAC

This sequence has the same length as the original but includes a different nucleotide (E instead of A in the 6th position). This also signifies a substitution mutation. Therefore:
[tex]\[ \text{substitution} \quad \text{CATTCACACG} \quad \rightarrow \quad \text{CATTECACAC} \][/tex]

Given the results, we can now match the sequences to their types of mutations:

[tex]\[ \begin{tabular}{|c|l|l|} \hline \text{Type of Mutation} & \text{Original Nucleotide Sequence} & \text{Changed Nucleotide Sequence} \\ \hline \text{deletion} & \text{CATTCACACG} & \text{CATTCACACA} (\text{or} \text{CATTCACG}) \\ \text{insertion} & \text{CATTCACACG} & \text{CATTCACACCACG} \\ \text{inversion} & \text{CATTCACACG} & \text{None (No inversion detected)} \\ \text{duplication} & \text{CATTCACACG} & \text{None (No duplication detected)} \\ \text{substitution} & \text{CATTCACACG} & \text{CATTTCACACG or CATTECACAC} \\ \hline \end{tabular} \][/tex]

Note: The sequences with mutations are listed as identified; in actual practice, further context might be required to pinpoint which sequence results from each specific mutation type.