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In mature mRNA, there is a start codon (AUG) that instructs ribosome to begin translation. Thereafter, every 3 bases are read as a "code word" calling for a particular amino acid to enlogate the polypeptide chain or to STOP and release the polypeptide. If 1 or 2 nucleotides are deleted or inserted into this sequence, it causes the reading frame to shift. This usually results in misreading of the sequence here is an example:

AUG - AGC - ACC - TAA - GGG - etc. (if we delete the first C we get....)

AUG - AGA - CCT - AAG - GG ( this is obviously not going to code for the same amino acid sequence)

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11y ago
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13y ago

Frameshift mutations are caused by the insertion or deletion of a number of nucleotides that isn't evenly divisible by three from a DNA sequence.

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Anonymous

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3y ago
any other causes

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11y ago

addition or deletion of one or more base pairs.

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11y ago

either an insertion or a deletion of a base

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9y ago

A mutation that results in a change in the codon reading pattern could result from the deletion or insertion of a base. This is also known as a frameshift mutation.

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9y ago

Mutations that would be considered frameshift mutations could be insertion and deletion.

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10y ago

A change up in amino acid sequences

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13y ago

Deletion or Insertion

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11y ago

problems in the dna

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Q: What mutations would be considered frameshift mutations?
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Related questions

What kinds of mutations are there?

point and frameshift


What are 3 genetic mutations?

substitution and deletion, frameshift, translocation


Name two major types of mutations?

Frameshift mutations and Point mutations. The difference between the two are that point mutations occur at a single point in the DNA sequence and frameshift mutations shift the "reading frame" of the genetic message.


Is pku a point shirt or a frameshift mutation?

PKU (phenylketonuria) is a point mutation, specifically an autosomal recessive genetic disorder caused by a mutation in the PAH gene. This mutation leads to impaired metabolism of the amino acid phenylalanine. It is not a frameshift mutation, which would involve an insertion or deletion of nucleotides, shifting the reading frame of the gene.


Two causes of mutation?

Two types of mutations are Point Mutations and the other is Frameshift Mutations. Piont mutations include; deletions, insertions, and substitutions. These mutations casue a slight change in the amino acid usually resulting in a change in one amino acid. The second type, frameshift mutations involve many changes and almost always results in many changes in the codons.


Are point mutations more harmful than frame shift mutations?

The Frameshift mutation affects more codons rather than in a point mutation depending on where it happens.


How many polypeptides would this DNA template code for?

There would be 5 polypeptide bonds if you are working on the "Whats the point?"-- Point frameshift, inversion, and Deletion Mutations worksheet.


What are the types of mutations that can occur?

nonsense mutation, missense mutation, frameshift muation, deletion or addition mutation


Mutations that cause dramatic changes in protein structure are often?

your mom is what causes the answer, Frameshift mutation.


What are the 4 types of mutations that can occur?

Insertion & deletion also known as frameshift mutationsubstitutionduplication mutationtranslocationGlad we could assist.


How would a protein be changed if a mutation caused a base to be added?

A mutation in which an extra nitrogen base is added is called a frameshift mutation. The rest of the sequence after the mutation will code for different amino acids, which will result in the alteration of the protein. Frameshift mutations cause severe genetic disorders.


Why do chromosome mutations occur most often during nuclear divisions?

Chromosome mutations occur during nuclear division because when the sequence of nucleotides are being placed substitutions, and frameshifts can occur, causing mutations. Substitution is when one nucleotide replaces another and frameshift mutation is when a nucleotide deletes, causing codons to be incorrectly read.