Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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1. In a couple of sentences, explain how eukaryotic activator proteins (that are usually gene-specific transcription factors) can enhance transcription even when bound to sequences hundreds or thousands of
2. Describe three common characteristics of transcription factors. The characteristics may relate to structure, or mechanism of action
(PLEASE ANSWER BOTH PLEASE)
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- 5. The following questions are about cis-regulatory elements (CRES). a. Describe the role of regulatory elements in eukaryotic gene expression b. What type of CREs are there? c. How do transcription factors 'know' where CREs are?arrow_forward33. For the following gene, which type of regulatory sequence has likely been deleted in mutant 1?arrow_forward6. explain what coupled transcription-translation is, and why it occurs in prokaryotes but not eukaryotesarrow_forward
- 1. Suppose there was a mutation in the inducer of the lac operon, such that the inducer was unable to function. How would the lac operon be affected? Please explain your reasoning in 1-3 sentences.arrow_forward1. What happens during transcription? Possible sentence frame: Transcription is the process in which the information from converted into This happens by isarrow_forward3. miR164 is a gene that encodes for a miRNA that targets a transcription factor. Describe in detail how, mechanistically, expression of miR164 could lead to altering the function of the transcription factorarrow_forward
- 13)arrow_forward4. The graph below was taken from a paper by Galardi et al., 2007, studying the role of two microRNAs (mIR-221 and mIR-222) in prostate cancer progression. The researchers identified that these cancerous cells have an upregulation in both mIR221 and miR 222. Use the graphs below to answer the questions A-B. Background: Panel A shows the nucleotide sequence of both miRs and a cell cycle inhibitor gene known as p27. Panel B shows protein levels of the p27 gene in three different cell lines, PC3 (a fast- growing cancer) and 22RV1 and LNCAP (two slow-growing cancers). A miR-221 3'-CUUUGGGUCGUCUGUUACAUCGA-5 ::: I : IIIII 1320-AUAGUUUUUACCUUUUAUGUAGCA -1: р27 Control miR-222 3-UCUGGGUC-AUCGGUCUACAUCGA-5 35 e P27 knock 30 down В p27 actin 48 Silvia Galardi et al. J. Biol. Chem. 2007:282-23716-23724 JBC time (h) Answer the following question(s): A. Summarize what you think the relationship between miR-221 and miR-222 with p27 in relation to the progression of cancer. B. If you were to develop…arrow_forward1. What features of a protein-coding gene might be found in a non-coding gene? 2. What features are unnecessary in a non-coding gene?arrow_forward
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