The functions of almost all of the genes in the lambda genome were first explored using mutations. What do you think the mutant phenotype would be if you made an inactivating mutation in the c gene, and why? Be very specific but also very brief.
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- How might a point mutation in DNA affect the phenotype. How the genome is expressed in the organism? (Please explain this at the molecular level).A certain Drosophila protein-encoding gene has one intron. If a large sample of null alleles of this gene is examined, will any of the mutant sites be expecteda. in the exons?b. in the intron?c. in the promoter?d. in the intron–exon boundary?Mobile genetic elements, such as the Alu sequences, are found in many copies in human DNA. In what ways could the presence of an Alu sequence affect a nearby gene?
- You have isolated a transposable element from the human genome and have determined its DNA sequence. How would you use this sequence to determine the copy number of the element in the human genome if you just had a computer with an Internet connection? (Hint: see Chapter 14.)When the human genome sequence was finally completed, scientists were surprised to discover that the genome contains far fewer genes than expected. How many genes are present in the human genome? Scientists have also found that there are many more different kinds of proteins in human cells than there are different genes in the genome. How can this be explained?If the coding region of a gene (the exons) contains 2,100 base pairs of DNA, would a missense mutation cause a protein to be shorter, longer, or the same length as the normal 700 amino acid proteins? What would be the effect of a nonsense mutation? A sense mutation?
- Not long ago investigators were surprised to learn that more than 95% of a mammalian genome is transcribed, even though less than 2% encodes proteins. What kind of evidence could be used to determine the percentage of the genome that is transcribed?What are the types of transposons? Please explain in detail how transposons contribute to genome evolution.A molecular geneticist hopes to find a Gene in human liver cell that codes for an important blood-clotting protein,he knows that the nucleotide sequence of a small part of the Gene is GTGGACTGACA.briefly explain how to obtain gene
- Consider a single base insertion mutation between the 3rd and 4th codons in a natural gene that encodes a protein 100 amino acids long. Is it more likely that the protein produced by this mutant allele will be shorter or longer than 100 amino acids long?Mutations in the CFTR gene result in cystic fibrosis in humans, a conditions in which abnormal secretions are present in the lungs, pancreas, and sweat glands. The gene was mapped to a 500-kb region on chromosome 7 containing 3 candidate genes. a)Using your knowledge of the disease symptoms, how would you distinguish between the candidate genes to decide which is most likely to encode the CFTR gene? b)How would you prove that your chosen candidate is the CFTR gene?Your friend has discovered that the same human promoter is responsible for producing two different proteins. In Kidney cells it is responsible for the production of protein A while in Brain cells it is responsible for the production of Protein B. Your friend has concluded that this promoter must be controlling two different genes. Do you agree or disagree with your friend's conclusion? Explain why or why not. Be sure to describe the molecular events to support your answer.