Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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34
The crystal structure has been determined for the complete 12-subunit yeast RNA polymerase II bound to a transcription bubble and product RNA.
Yes
or
no
35
( ) can be used to purify transcription activator proteins
36
A mutation that adds or deletes a base pair in the open reading frame and is termed a ( ) mutation.
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- The oxidation of guanine bases in the context of triplet repeats such as CAGCAGCAG can lead to the expansion of the repeat. Explain.arrow_forwardQuestion:-arrow_forwardIn which direction along the template must theRNA polymerase in Figure Q6–1 be moving to have gen-erated the supercoiled structures that are shown? Wouldyou expect supercoils to be generated if the RNA poly-merase were free to rotate about the axis of the DNA as itprogressed along the template?arrow_forward
- In Figure 12-26, provide a biochemical mechanism forwhy HP-1 can bind to the DNA only on the left side of thebarrier insulator. Similarly, why can HMTase bind onlyto the DNA on the left of the barrier insulator?arrow_forwardPlease answer need helparrow_forwardIn bacteria, a transcription experiment in vitro with purified RNA polymerase holoenzyme is fairly straightforward. In eukaryotes, it is not. Explain this observation, including what would be meant by the term “holoenzyme” for a eukaryotic RNA polymerase.arrow_forward
- Mcm2 is a protein of the helicase complex that recognizes origin in Eukaryotes. But it is also related to cancer progression in humans. Please describe the role of Mcm2 in cancers and the potential uses of its inhibition in cancer treatment.arrow_forward18 Actin can be used as a loading control in a western blotting experiment. What is the purpose of a loading control?arrow_forwardPlease asaparrow_forward
- What are two possible anticodon sequences for tRNA's that are charged with Phenylalanine (Phe)? O 3' AAU 5' and 3' GAA 5' O 3' AAA 5' and 3' AAG 5 3' UUG 5' and 3' CUG 5' O 3' GAA 5' and 3' CAG 5' 3' GUA 5' and 3' GUG 5'arrow_forwardTable 1 shows a list of restriction endonucleases with their recognition sequence and the sites of cleavage indicated by arrows. Table 1 Enzyme name Recognition sequence and position of cut 5'GIAATTC3 5'G!GATCC3' 5'GIGTACC3 5'GCIGGCCGC3' 5'IGATC3' 5'GGTACIC3' 5'ALGATCT3 EcoRI ВатHI Аcс651 Notl Sau3A Kpnl BglII (i) Which restriction enzyme(s) produce blunt ends? (ii) Are there any pair of neoschizomers in the list? Explain. (iii) Are there any pair of isocaudomers in the list? Explain.arrow_forwardYou have recently cloned multiple cDNAs for a gene you are studying. After sequencing ten of the cDNAs, you find that seven of the cDNAs would produce a protein of 531 amino acids, while the other three cDNAs would produce a protein missing 30 amino acids from the center of the protein. This finding is can be explained by: O nonsense suppression O alternative splicing O basepair wobble O variability in the length of the poly(A) tailarrow_forward
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