Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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A protein called trypsin, which plays a role in digestion, is made by
pancreatic cells and secreted from those cells. Starting with a sample
of pancreatic cells, a researcher modified the gene that encodes trypsin by mutating the ER signal sequence so it was no longer recognized by SRP. How would this mutation affect the targeting of trypsin?
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- A KDEL sequence is a sequence of amino acids in a protein that binds a KDEL receptor, which helps recycle it back to the ER. Name two techniques a scientist could use in combination to experimentally demonstrate the function of a KDEL sequence. (To help you think about how to answer this: What would happen if the KDEL sequence were nonfunctional? How could you observe the result?) Please answer this and thank you!arrow_forwardThe activator (V protein) that is present in the bacterial cell is normally phosphorylated, but only binds to the A site in the operon when it is not phosphorylated. What operon-independent mechanism can regulate the binding of (and also ultimately regulates the removal of) protein V to the A site? Describe this binding/removal mechanism in detail – useappropriateterminologythatwasdiscussedinlecture. Aspartofyouransweraboutthisactivatorproteinbindingto (and then detaching from) the A site of the operon, be sure to address what are the results of this type of control in terms of function of the operon.arrow_forwardZeb1 encodes a transcription factor that activates expression of genes that help cells migrate (move to different parts of the body) during embryogenesis. Zeb1 is not expressed in most adult tissues, but can undergo a gain of function mutation in some tumors. Which change is likely to result from a gain of function mutation in Zeb1? a) sustaining proliferative signalling b) activating invasion and metastasis O c) deregulating cellular energetics O d) resisting cell deatharrow_forward
- Mutation in the fibroblast growth factor receptor (FGFR) gene results in achondroplasia (dwarfism), which is a dominant condition caused by a single base substitution (GGG>AGG) that changes the amino acid glycine at position 480 to arginine (G480R) in the FGFR protein. FGFR is normally active when FGF binds to it, but the mutant FGFR is always on to stimulate signaling that inhibits excessive bone growth. How can gene therapy be used to treat achondroplasia? Select all that apply. RNAi that knocks down the mutant FGFR expression Adeno-associated viral (AAV) vector that carries the wild-type FGFR Retroviral vector that carries the wild-type FGFR CRISPR with the wild-type FGFR donor DNAarrow_forwardWhich of the following molecules will experience a large change in cytoplasmic concentration whenthe above tryptophan operon is turned on (in E. coli cells)?A. tryptophan molecules will decrease in concentrationB. lactose molecules will decrease in concentrationC. tryptophan molecules will increase in concentrationD. lactose molecules will increase in concentrationE. none of the abovearrow_forward
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