What would be the most likely effect of a mutation in each of the following in an E. coli genome? (A) -8; (B) -35; (C) -20; (D) Start site.
Answer:
(A) Mutation at the -8 position would probably affect the -10
consensus sequence (TATA box), which is centered on the position
-10. This sequence is necessary for the binding of RNA polymerase.
A mutation there would most likely cause a decrease in
transcription.
B) A mutation in the -35 region could affect the binding of sigma
factor to the promoter. Transcription would probably be reduced or
inhibited.
C) The -20 region is located between the consensus sequences of an
E.coli promoter. A mutation here may not have any effect
on transcription.
D) A mutation in the start site would have little effect on
transcription. The position of start site relative to the promoter
is more important than the sequence at the start site.
What would be the most likely effect of a mutation in each of the following in...
Which of the following mutations would be most likely to have a harmful effect on an organism? (A) a deletion of three nucleotides near the middle of a gene (B) a single nucleotide deletion in the middle of an intron (C) a single nucleotide deletion near the end of the coding sequence (D) a single nucleotide insertion downstream of, and close to, the start of the coding sequence In this problem, why (c) cannot be the answer?? Single nucleotide deletion...
Match the following phenotypes with the mutation that would be the most likely to be its cause. The mutant proteins are listed below, followed by the protein domain that is mutated in each case, followed by the amino acid change that is a result of the mutation Try to answer each question by using the following reasoning: if you observe a phenotype, then that could be due to a mutation in protein in which the domain has had an amino...
Q17 Homework – Unanswered What type of physical mutation would most likely occur as a result of exposure to Oxygen free-radicals? o A nonsense O B missense 0 C silent O D polymorphism O E frameshift
Q14 Homework. Unanswered What type of physical mutation would most likely occur as a result of X-ray exposure? o A nonsense 0 B missense - nonsynomous o C missense - synomous o D silent O E polymorphism O F frameshift
What would be the most likely effect on the transcription of the trp structural genes for the following mutations? mutation that prevents ribosome binding to the mRNA 5' UTR mutation that changes region 1 tryptophan codons into alanine codons mutation that creates a stop codon in region 1 of mRNA 5' UTR deletions in region 2 of the mRNA 5' UTR deletions in region 3 of the mRNA 5' UTR deletions in region 4 of the mRNA 5' UTR deletion...
What would be the effect of each type of the following mutations? a,) Mutation that destroys the function of eukaryotic DNA polymerase alpha. b.) A mutation that destroys the 5' to 3' exonuclease activity of DNA polymerase I.
What would the most likely phenotype of an E. coli colony containing pUC18 (without an insert fragment) be if the following de novo mutations occurred early in the growth of a single cell into a colony on your plate (assuming plate contains X-gal, IPTG and Amp)? a. A frameshift mutation in the fifth codon lacZ gene in pUC18. b. A loss of the pUC18 plasmid. c. A deletion of bps at positions 19-25 of the ampicillin resistance gene open reading...
If a mutation occurs as a result of X-ray exposure, what genetic classification of mutation would most likely occur? A hypomorph B hypermorph C neomorph D antimorph E amorph F frameshift G haploinsufficient
In terms of the Trpoperon, where would the Trp operon repressor protein most likely bind? Drag the "Trprepressor" label to the location where that repressor protein is most likely to bind and exert its effect on the system. (A Trprepressor Trp operon Trp operator F D C B A E. coli DNA promoter mRNA molecule series of enzymes required for tryptophan biosynthesis
1. Which of the following mutations is the most likely to be neutral? A) A nonsense mutation in exon 5 of a gene with 39 exons. B) A splice site mutation in intron 3 of a gene with 8 introns and 9 exons. C) A single nucleotide insertion in exon 7 of a gene with 18 exons. D) A thee nucleotide deletion in exon 1 of a gene with 7 exons.