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Ch. 13 - The Genetic Code and Transcription

Chapter 13, Problem 28

While miRNA response elements (MREs) may be located anywhere within an mRNA, they are most often found outside the coding region in the 5' or 3' UTR. Explain why this is likely the case given that miRNAs often target more than one mRNA.

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Hi, everybody. Let's take a look at this practice problem together. Micro RNA, S M I R N A s are a class of non coding RNA is that play important role in the regulation of gene expression. One single M I R N A usually targets many genes and one gene might be regulated by multiple M I R N A s. The reason for multiple targets is recall that M I R N A plays a role in the regulation of gene expression how by binding their target M R N A s. So the reason for multiple targets is what is it A M I RNA binding sites included, not only three prime untranslated regions, but also five prime untranslated regions and coding sequences. So that's a long one and we'll come back to that be short base pairs within M I R N A three prime untranslated region duplex C, both A and B or dean, none of the above. Now, let's discuss a further and I'd like to review a depiction of M RNA with the regions mentioned in a. Here, we have an M RNA strand, We have the five prime end a five prime untranslated region, A coding sequence, a three prime untranslated region. And then the three prime end, typically, when M I RNA binds, it creates a duplex and binds to the three prime untranslated region. However, it can also bind the coding sequence as well as the five prime untranslated region. So here alone on this single M RNA strand, there's 123 different possibility of the M RNA targeting and binding this M RNA strand. Therefore, a is a true statement and one of the reasons for multiple targets. Now let's talk about B short based pairs with an M I R N A three prime untranslated region duplex. So that's referring to when the M I RNA binds here with the three prime untranslated region. Now, it's important to note that when it binds, it does not have to have perfect binding to the target. M RNA is the binding, however, does have to be perfect within a region called a seed region. What is the seed region? Well, it is on the M I R N A, It's closer to the five prime end And it's usually 6-8 nucleotides long. So when M I RNA binds its target M R N A, that seed region has to have perfect binding. Other sections may not have perfect pairing or perfect binding. So given this short number of bases within the seed region and considering the vast amount of bases in the human genome, that means M I R N A s can easily bind hundreds of targets. So B is also true. Therefore, the correct answers options. See both A N B. Alright, everyone. Thanks for hanging in with me. I know this video is a bit of a longer one. I hope you found it helpful though and I'll see you next time for the next practice problem.
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The interphase nucleus is a highly structured organelle with chromosome territories, interchromatin compartments, and transcription factories. In cultured human cells, researchers have identified approximately 8000 transcription factories per cell, each containing an average of eight tightly associated RNAP II molecules actively transcribing RNA. If each RNAP II molecule is transcribing a different gene, how might such a transcription factory appear? Provide a simple diagram that shows eight different genes being transcribed in a transcription factory and include the promoters, structural genes, and nascent transcripts in your presentation.

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RNAi is currently being tested as a therapeutic tool for genetic diseases and other conditions. Consider the following: cystic fibrosis caused by loss of function of the CFTR gene, HIV infection, and cancer caused by hyperactivity of a growth factor receptor. Which of these may be treatable by RNAi, and which not? Explain your reasoning.

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Explain how the expression of a single gene can be quickly, efficiently, and specifically shut down at the transcriptional, posttranscriptional, and posttranslational stages through the coordinated expression of a transcriptional repressor, an miRNA, and a ubiquitin ligase.

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Recent observations indicate that alternative splicing is a common way for eukaryotes to expand their repertoire of gene functions. Studies indicate that approximately 50 percent of human genes exhibit alternative splicing and approximately 15 percent of disease-causing mutations involve aberrant alternative splicing. Different tissues show remarkably different frequencies of alternative splicing, with the brain accounting for approximately 18 percent of such events [Xu et al. (2002). Nucl. Acids Res. 30:3754–3766].

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