a. What percent of the genome is thought to be functional, if including RNA? What role does the transcriptome (and specifically microRNAs) play in the cell?
b. Describe the process of microRNA function. What is the difference with regards to the source of miRNA and siRNA?
a. Not more than 25 percent of the genome is functional at least in case of humans and rest of them is known as true junk DNA as they are harmless and useless and also because their function is still not known.
Transcriptome can be regarded as the total RNA molecules in a cell or a population of cells. It can be also regarded as the subset of proteome which is the total protein content of the cell. Unlike genome content transcriptome can vary in a given cell depending on varying conditions such as stress, any developmental change etc. the transcript level reflects the genes that are actively expressed or repressed except for the RNA degradation.
microRNAs are small 22 nucleotides RNA which do not code for any protein and basically are involved in regulatory processes at the post transcriptional level by inhibiting or repressing the function of the RNA.
b. MicroRNAs are small non coding RNA which play regulatory role at the posttranscriptional level. They are evolutionarily conserved and they are transcribed by RNA pol II or pol III forming precursors which is then cleaved sequentially to form the final mature micro RNA. The function of microRNA is achieved through two ways: one is RNA degradation and the other is translation inhibition. In both the cases the silencing is mediated through a complex formation called as RISC (RNA induced silencing complex). When Extensive base base pairing occurs between target RNA and microRNA occurs it leads to fragmentation of the RNA finally degrading it whereas minimal base pairing of the target RNA and the microRNA results in translational repression.
Both miRNA and siRNA can lead to gene silencing. miRNA is typically produced endogenously inside the cells and are single stranded whereas siRNA are double stranded and are taken up by the cells exogenously through viruses or external vectors, plasmids.
a. What percent of the genome is thought to be functional, if including RNA? What role...
Question 2: The RNA interference (RNAi) pathway was discovered in C. elegans in 1993 and hs since rapidly towards therapeutic applications, including the first approved RNAi therapeutic in August of 2018. Use your u of RNAi and its therapeutic applications to answer the questions below. (A) Compare and contrast the short interfering RNA (siRNA) and micro-RNA (miRNA) processes. In what ways are these two RNAi pathways similar? In what ways do they differ? (8 points) (B) Suppose you work for...
1. The virus hijacks the cell, and RNA polymerases produce the complement to the positive stranded RNA genome. We can call these strands negative strands, and they then serve as templates for RNA polymerases to produce their complement. How does the sequence of these strands, the complement to the negative strands, compare with the original viral genome? 2-1. RNA polymerases lack proofreading ability. Define proofreading ability and describe its importance in replication of DNA genomes. a. Why is this a...
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b) What property p it to be functional"? Explain your sr Detity (or properties) of R be replcafec Snl sh RNA c) Which of t a "functional RNAz Chthe folowing CRN mNAR (2pts) Either: i) Pick any two types what ea d) at are functional RNAs, and briefly state each one does (make clear which two you have chosen), or i) Name the three types y of RNAs that participate in translation, and state what role each plays in this...
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LUIS 15 12. What are the 3 types of RNA? What is the role of each of them in translation? 13. Briefly describe what happens during the steps of translation 1. Initiation of translation 2. Elongation 3. Termination of translation 14. The base sequence of the gene coding for a short polypeptide is the following: TA CGC TAGGCGATTGACT A. What would be the base sequence of the mRNA transcribed from this gene? B. Using the genetic code given out...
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1. Describe one experiment that can test the hypothesis that DNA replication is semi conservative. Describe the results of this experiment if replication was conservative. And if it was distributive? 2. What type of chemical bond contributes to the specificity of base paring in the DNA? Are there any other chemical or physical factors in the structure o f the DNA molecule contributing to the thermodynamic stability of the DNA? 3. List the m ajor differences between DNA and RNA....
1) You are a studying the prog ression of cells through the cell cycle. You are particularly interested in the role of the APC, which in a ubiquitin E3 ligase, in the control of the metaphase cyclin (cyclin B) and the timing of events. To look at this you start by synchronizing your cells in G1 and examining the levels of Cyclin B over time. The APC usually works on cyclin B during anaphase. RBX57 is a substrate for Cylcia...