It is assumed that the transcript is the mature mRNA fully prepared for translation.
Single Nucleotide Addition at position 100 - this region could fall in the 5'-UTR region and in that case it might not get expressed in the encoded protein. However, if this region falls in actual coding region it will cause frameshift mutation and a non-functional protein will be formed or a truncated protein or a mis folded protein.
Single Nucleotide Addition at position 600 - the effect would be most disastrous as this region falls in very mid of actual coding region. The single nucleotide addition will cause a frameshift mutation and will disrupt the whole sequence of amino acids in the protein. The protein to be encoded could be now a truncated protein or mis-folded or just non-functional. Any thing can happen in such case.
Single Nucleotide Addition at position 1150 - this would probably have no effect on the protein translated as this region will fall in 3'-UTR
Single Nucleotide Addition inside intron - this addition will have no effect at all as all introns are removed during splicing.
answer please! A gene is coded by a transcript that is 1200 nucleotides long. What would...
A gene is coded by a transcript that is 1200 nucleotides long. What would be the effect on the protein encoded by this gene, of a single nucleotide addition at position 100, position 600 or position 1150? And what would happen if that addition was inside an intron?
Question 2: Transcription, RNA Processing and Translation A particular gene codes for a mature mRNA transcript containing 1200 bases, which is translated into a protein containing 300 amino acids. A. How long is the coding sequence in this mRNA and how many nucleotides are in the UTRs? For the purposes of this question we are ignoring the G’ cap and the polyA tail. B. A mutant form of the gene created by one nucleotide being changed to another nucleotide also...
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...
3of 3 9. The figure below represents the primary transcript of a gene that contains four exons (A, B, C, D) and two introns. The dark block in exon B indicates the position of an additional stop codon; the normal start and stop codons for translation are present in exons A and D respectively. The two arrows indicate alternative 3' splice sites for the first intron Pre-mRNA 5'I 3' intron intron Give a schematic representation of the mature mRNAs that...
Part A A particular mRNA is 300 nucleotides long. If a mutation in the middle of the sequence changed a codon from a AAA to a UAA then what would be a reasonable prediction 0 The protein coded by his mRNA would be longer O The protein coded by this mRNA would kilthe cell O The protein coded by this mRNA would be the same size O The protein coded by this mRNA would be shorter O The protein coded...
why is E the answer Below is the genomic DNA of gene X, a 3 exon gene that encodes a 131 amino acid single pass transmembrane protein. Shown are the transcriptional start site, splice donor, acceptor and branch sites and translational start and stop codons. Transcriptional start EXON 1 INTRON 1 EXON 2 INTRON 2 EXON 3 Spfice Donor Splice Acceptor Polyadenylation signal Branch point 17. Treatment with ethidium bromide, an intercalating agent, caused DNA polymerase to add an extra...
please answer all parts 25) A few points: Explain how a single nucleotide substitution in the sequence of a gene can: A) cause a mutation (a single amino acid replacement) in the protein coded by the gene and B) how such a single nucleotide substitution does not necessarily lead to a mutation in the protein (a silent mutation). Be very specific and use real examples for the nucletotides and the resulting amino acid in the protein. You must provide the...
1) During splicing what would happen if the 'AG' splice siteseqeunce was mutated to 'AT'? Less RNA would be removed (Ie: more RNA would be included in the final transcript) More RNA would be removed (ie: less RNA would be included in the final transcript) The Branchpoint A in the intron would be unable to attack its splice site, so no splicing would occur at this location No changes would occur 2) iPSCs are identified by the production of a...
Genetics Worksheet Week 3: Gene Regulation and Epigenetics 1. Duchenne muscular dystrophy is caused by a mutation in a gene that is 2.5 million nucleotides in length and encodes a protein called dystrophin. The dystrophin protein itself is 3684 amino acids in length. Calculate below the approximate size of the mRNA that encodes dystrophin. Approximately what percentage of the gene that encodes dystrophin is intron sequence? The human genome encodes a much greater variety and number of proteins than the...
5. Consider the wild-type F8 gene. What would happen to the 1) transcript (mRNA) sequence and quantity, 2) to the protein (sequence, quantity, function) and 3) the person’s overall phenotype if they were homozygous (both copies of the gene are the same) for a 3 base-pair deletion in the: i. First intron ii. First exon iii. The promoter iv. 5’UTR v. Last exon 6. What environmental factor could affect the phenotype caused by an F8 null mutation? Thrombophilia is a...