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Drag each label to the correct location.

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

Original Nucleotide Sequence: CATTCACACA
Changed Nucleotide Sequences:
1. CATTCACACCACE
2. CATTTCACACE
3. CATTCACE
4. CATTGCACAC

\begin{tabular}{|l|l|l|}
\hline
Type of Mutation & Original Nucleotide Sequence & Changed Nucleotide Sequence \\
\hline
Deletion & CATTCACACA & CATTCACE \\
\hline
Insertion & CATTCACACA & CATTCACACCACE \\
\hline
Inversion & CATTCACACA & CATTGCACAC \\
\hline
Substitution & CATTCACACA & CATTTCACACE \\
\hline
\end{tabular}


Sagot :

Sure, let us match the given nucleotide sequences to the types of mutations.

Original Nucleotide Sequence: CATTCACACA

Changed Nucleotide Sequences:
- CATTCACACCACE
- CATTCACE
- CATTGCACAC

### Step-by-Step Solution:

1. Insertion Mutation:
- Changed Sequence: CATTCACACCACE
- This sequence has extra nucleotides compared to the original. Specifically, it has an additional "C" and "E" at the end.
- Type of Mutation: Insertion
- Match: Insertion Mutation changes CATTCACACA to CATTCACACCACE

2. Deletion Mutation:
- Changed Sequence: CATTCACE
- This sequence is missing parts of the original sequence. Specifically, the "ACA" segment is missing.
- Type of Mutation: Deletion
- Match: Deletion Mutation changes CATTCACACA to CATTCACE

3. Substitution Mutation:
- Changed Sequence: CATTGCACAC
- This sequence has a single nucleotide change compared to the original. Specifically, the "T" in the 5th position is replaced by a "G".
- Type of Mutation: Substitution
- Match: Substitution Mutation changes CATTCACACA to CATTGCACAC

### Tabulated Form:

\begin{tabular}{|l|l|l|}
\hline \begin{tabular}{c}
Type of Mutation
\end{tabular} & \begin{tabular}{c}
Original Nucleotide \\
Sequence
\end{tabular} & \begin{tabular}{c}
Changed Nucleotide \\
Sequence
\end{tabular} \\
\hline \textbf{Deletion} & CATTCACACA & CATTCACE \\
\hline \textbf{Insertion} & CATTCACACA & CATTCACACCACE \\
\hline \textbf{Substitution} & CATTCACACA & CATTGCACAC \\
\hline
\end{tabular}

By matching correctly, we clearly understand how each type of mutation affects the original nucleotide sequence.