6. You are studying an anaerobic, unicellular eukaryote that lacks mitochondria. Strangely, the nuclear DNA of these cells is shown to contain genes that are very closely related to a number of mitochondrial genes. What is a possible explanation for this odd finding?
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- A major difference between hereditary information in eukaryotes and prokaryotes is: a. in prokaryotes, the hereditary information is distributed among individual, linear DNA molecules in the nucleus. b. in eukaryotes, the hereditary information is encoded in a single, circular DNA molecule. c. in prokaryotes, the hereditary information is usually distributed among multiple circular DNA molecules in the cytoplasm. d. in eukaryotes, the hereditary information is distributed among individual, linear DNA molecules in the cytoplasm. e. in eukaryotes, the hereditary information is distributed amoung individual, linear DNA molecules in the nucleus.In 2016, scientists published the genome of Monoceiconionoides, and demonstrated that this organism has no detectable mitochondrial genes. However, its genome was arranged in linear chromosomes wrapped around histones which are contained within the nucleus. Monoceiconionoides is therefore a(n). Bacteria Archea Eukaryote Endosymbiont1. Peroxisomes are organelles surrounded by a single membrane. Soluble proteins that reside within peroxisomes are imported post-translationally, and they often contain the C-terminal tripeptide SKL (serine-lysine-leucine). a) How would you confirm that a C-terminal SKL tripeptide is a peroxisomal targeting signal? b) If cells were engineered to produce a hybrid protein consisting of a mitochondrial matrix protein (including its signal sequence) followed by a C-terminal SKL signal, where in the cell would you expect the hybrid protein to be found? Explain your reasoning.
- I have this same question, but the answer is supposed to involve mitochondrial uncoupling?3. Consider the pathway for the synthesis of the amino acid arginine in Neurospora: ARG-F. → ARG-E → citrulline ARG-H ornithine Mutant strains of Neurospora are grown in minimal media supplements as follows. Each mutant strain carries only a single mutation. Growth is shown by (+), no growth is shown by (o). → argininosuccinate > arginine Supplements citrulline arginino- succinate mutant nothing Qraitibine arginine strain +. Indicate the correct strain / defective gene pairing. a) strain a / ARG-F b) strain a/ ARG-H strain b / ARG-F d) strain c / ARG-E e) strain c / ARG-F + + +10. In eukaryotic cells, glycosylation activity of membrane proteins is found in the lumen of the endoplasmic reticulum (ER) and is accomplished by the enzyme oligosaccharyl transferase (OST), which adds oligosaccharides to the amino group of Asn residues of the consensus sequence Asn-X-Thr/Ser. a. The following ER membrane protein construct has a cytosolic N-terminal region and a membrane-spanning variable sequence. The variable sequence is a signal anchor (SA) sequence. Would you expect the C-terminal region of the B subunit to be glycosylated? Why or why not? variable sequence C-terminal region of B-subunit N-terminal region b. An additional transmembrane region is added to the construct prior to the variable sequence, as shown below. The transmembrane is a signal anchor (SA) sequence, while the variable sequence is a stop transfer anchor (STA) sequence. Would you expect the C-terminal region of the B subunit to be glycosylated? Why or why not? C-terminal region of B-subunit…
- 8. In genetic screens of mutagenized yeast, temperature sensitive mutants defective in the secretory pathway (sec mutants) were identified. These mutants have helped scientists study the protein secretion pathway that is necessary/essential for life in eukaryotic cells. To identify sec mutants: mutagenized yeast cells were grown for 12 hours at low temperature, shifted to higher temperature for two hours, and then the population of cells were centrifuged in a density gradient. a. Mutagenized cells were first grown at the lower temperature and then shifted to the higher temperature. i. Why was the shift in temperature an important step of the experimental protocol? ii. Why would the experiment have been unsuccessful if the cells were grown exclusively at the higher temperature? b. After centrifugation, where would sec mutant cells be located compared to other cells in the population? Briefly explain why.8. The R121M mutant complex I has the ability to accept protons but cannot pass them to ubiquinone. Assume mitochondrial membranes are assembled containing the R121M complex I, plus wildtype complexes II, III, IV and V. If FADH2 is provided, which complexes will be reduced? Circle all that apply а. R121MComplex I b. Complex II с. Complex II d. Complex IV e. Complex V f. None of the complexes will be reduced tes) D Focus w 83°F DELL F10 F11 F12 PrtSc F4 F5 F6 F7 F8 F91. Lysosomal hydrolases contain sorting signals that mark these proteins for modification with mannose 6-phosphate. Lysosomal sorting signals are unusual in that they are not peptides attached to the termini of the proteins. Instead, lysosomal sorting signals are “patches” on the folded proteins. Such a signal patch may include amino acids that are distant from one another in the linear polypeptide chain, but are brought close together by protein folding. When cell biologists identify a sorting signal, they confirm that the signal isnecessary and sufficient. Suppose that you have identified a putative signal patch on a lysosomal hydrolase. How would you test whether this signal is necessary and sufficient to mark the protein for modification with mannose 6-phosphate? 2. By combining microscopy, biochemistry, and genetics, researchers have identified clathrin-coated vesicles that mediate endocytosis and TGN-to-endosome transport, as well as COPII vesicles that mediate ER-to-Golgi…
- 1. Lysosomal hydrolases contain sorting signals that mark these proteins for modification with mannose 6-phosphate. Lysosomal sorting signals are unusual in that they are not peptides attached to the termini of the proteins. Instead, lysosomal sorting signals are “patches” on the folded proteins. Such a signal patch may include amino acids that are distant from one another in the linear polypeptide chain, but are brought close together by protein folding. When cell biologists identify a sorting signal, they confirm that the signal is necessary and sufficient. Suppose that you have identified a putative signal patch on a lysosomal hydrolase. How would you test whether this signal is necessary and sufficient to mark the protein for modification with mannose 6-phosphate?39. What makes it possible for human mitochondria, which have only 22 sequences that code for tRNA, to translate mitochondrial polypeptides that require 32 tRNAs?Transposable elements, “jumping genes”, were first described by Barbara McClintock in her Nobel prize winning studies with corn. The genome of every multicellular eukaryote that has been sequenced is composed of a large percentage of transposable elements (often 30% to 50%), but they are nearly absent from the genomes of eubacteria and archaea. What are these things and what do they do? Describe and draw the structural organization and mechanism for movement of transposons and retro- transposable elements. What effect do these elements have on the stability of genomes? can you help me answer the bolded question?