Which of the Following Can Result in a Frameshift Mutation

Along with substitutions mutations can also be caused by insertions deletions or duplications of DNA sequences. A frameshift mutation is a genetic mutation caused by a deletion or insertion in a DNA sequence that shifts the way the sequence is read.

Genetic Mutations Active Reading Genetics Genetic Mutation Mutation

Students use CRISPRCas9 and nonhomologous end joining to generate frameshift insertion and deletion mutations in the CAN1 gene which are easily selected for using media plates that have canavanine.

. Which of the following can result in a frameshift mutation. The gene expression is performed by codons either by insertion or deletion of a base which can change the reading frame of sequencehence the frameshift mutation occurs. Which of the following is an example of a frameshift mutation.

A frameshift mutation can result from the addition of a nucleotide to a sequence. And thats important because the cell reads a gene in groups of three bases. Frameshift mutations can lead to the following outcomes.

What type of gene mutation results from the insertion or deletion of nucleotides and alters the entire amino acid sequence from that point forward. You will need a codon chart. Mechanism of Frameshift Mutation.

1 Point A deletion of a codon A deletion of a nucleotide A substitution in the third codon An insertion of a codon 11 Which vitamin is required for synthesis of the blood clotting proteins. Deletion Strand Taking out the first G in the original DNA above results in. A frameshift mutation is a particular type of mutation that involves either insertion or deletion of extra bases of DNA.

Which of the following types of mutations could result in a frameshift mutation. Missense mutations are a type of frameshift mutation. The number of bases that are either added or subtracted cant be divisible by three.

But the following are some of the possible mechanisms of frameshift mutation. Deletion of the DNA segment occurs in anaphase movement or during reorganizing of the nuclei or digestion by nucleases. As a result a variety of metabolic processes may be disrupted.

DNA sequencing is also performed to determine what type of mutation occurred in gene-edited cells. Either an insertion or a deletion of a base a base insertion only a base deletion only deletion of three consecutive bases a base substitution only. It usually only changes one amino acid in the protein coded for by a gene.

Which of the following can result in frameshift mutations-alkylating agent-tautomeric shift -base analog-acridine dye -deamination. They change all the codons from the mutation on down the line which changes the amino acid sequence Which of the following would result in a frameshift mutation. A frameshift mutation can result from a deletion of a nucleotide to a sequence.

Mutations are categorized by. GCA ATG CAC mRNA. Which of the following can result in frameshift mutations.

A purine is replaced by another purine and a pyrimidine is replaced by another pyrimidine. So the correct answer is Either an insertion or a deletion of a base. An insertion or deletion can result in a frameshift mutation.

Circle each correct answer. Frameshift mutation nearly always results in a nonfunctional protein because every amino acid after the mutation is different from what was coded for in the original DNA. Which of the following would result in a frameshift mutation.

Frameshift mutation nearly always results in a nonfunctional protein because every amino acid after the mutation is different from what was coded for in the original DNA. Now whats important here is the number three. Therefore frameshift mutations result in abnormal protein products with an incorrect amino acid sequence that can be either longer or shorter than the normal protein.

Missense mutations are a type of frameshift mutation. A frameshift mutation can result from the deletion of three nucleotides from a sequence. The sequence of the DNA remains the same since the change involves proteins.

The sequence of three nucleotides of either DNA or RNA is known as a codon. So the correct answer is Either an insertion or a deletion of a base. An abrupt halt to the translation process results in non-usable protein which has ramifications for the physiological systems involved.

A base pair is added to the DNA within a gene which causes a reading frame shift. DInsertion or deletion of nucleotides that results in a premature stop codon The answer is C because a frameshift mutation indicates that the reading frame of the sequence in altered resulting in production of different codons. Can someone help me with this please.

A protein with a changed coding sequence may be unusable or a totally different protein. A base pair is lost within the DNA of a gene which causes a reading frame shift. Mutations are categorized by.

To demonstrate this complete the following. 1 Point Cholecalciferol Phylloquinone Retinoic acid Tocopherol The central dogma of molecular. A frameshift mutation can occur with either _____ or _____ mutations.

Mutations can be caused by all of the following except. 11 Questions Show answers. The gene expression is performed by codons either by insertion or deletion of a base which can change the reading frame of sequencehence the frameshift mutation occurs.

The mechanism of frameshift mutation depends on the cause of the mutation.

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