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Yes. Nucleotides are read in triplet code (i.e. AAA, CCC) and each set of three nucleotides represents an amino acid. Therefore if you had a line of nucleotides, and you removed or added one in the line you would be changing how the code is read. Observe if you had ACGAGUGAU. It is read as ACG-AGU-GAU - which represents threonine-serine-aspartic acid. Now, if we remove the first A, the new code is CGAGUGAU to which the reading frame is - CGA-GUG-AU. This would even change the amino acids the code was describing. It is now - Argenine-Valine and an incomplete third code.

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Q: Is it true point mutations that involve the insertion or deletion of a nucleotide change the reading frame of the genetic message?
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Related questions

What are the types of genetic mutations?

1. Insertion- when a nucleotide gets added to the DNA strand2. Substitution- when a nucleotide gets replaced on the DNA strand3. Deletion- when a nucleotide gets deleted from the DNA strandThose are all of the DNA mutation types. Hoped this really helped you out


What is a point mutuation?

A point mutation is a type of genetic mutation that involves a change in a single nucleotide base pair in DNA. This can result in the substitution of one nucleotide for another, the insertion of an extra nucleotide, or the deletion of a nucleotide. Point mutations can lead to changes in the amino acid sequence of a protein, which can affect its structure and function.


What are 3 genetic mutations?

substitution and deletion, frameshift, translocation


What are the various kinds of mutations?

Mutations differ and change according to many factors: 1- Site of occurrence: -Genetic mutations -Chromosomal mutations 2- The inheritance: -Somatic mutations -Gamete mutations 3- The origin: -Spontaneous (natural) mutations -Induced mutations 4- The harmful OR useful effects: -Undesirable mutations -Desirable mutations


What are the causes of genetic human disorders?

The causes of genetic disorders areThey can be inherited through Parents;Mutations may occur;A deletion may occur.These are the causes of a genetic disorder.


Define a genetic mutation and state the types of genetic mutations?

Point mutation: single nucleotide is replaced with another. ex: sickle cell anemia.


How is the term insertion properly defined?

'Insertion' is a therm in genetic science. It describes the addition of nucleotide base pairs into DNA sequences. It might lead to a hazardous mutation of the DNA.


What is an example sentence with deletion?

Examples include:Concerning genetic mutations, a deletion that occurs towards the beginning of a gene sequence is more detrimental than one that occurs towards the endWith the deletion of all vowels, Tim rendered his sentence unreadable


Where are Kmart corporate offices in Puerto Rico?

A type of genetic mutation in which one or more base pairs are lost: (IS IT REPLACEMENT, SUBSTITUTION, DELETION, INSERTION).


Why do mutations tend to be harmful instead of helpful?

Not all mutations are harmful. The improvements in creatures through evolution are from beneficial mutations. The beneficial mutations increase the creature's chance of survival and passing along those new beneficial genes to its offspring.


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.


What are two types of frame shift mutations?

"I believe there is insertion and deletion, (one kind), and substitutions. (the second kind)" This answer is incorrect, the two types of frameshift mutation are insertion and deletion, these both alter the translation reading frame. A substitution point mutation in DNA is referred to as a single-nucleotide polymorphism and does not result in any change to the translational reading frame. insections and deletions are two types of frameshift mutations