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post transcriptional regulation khan academy

1 Passage 5 Question 28. The genes that a eukaryotic cell turns “on” largely determine its identity and properties. If you're behind a web filter, please make sure that the domains *.kastatic.org and *.kasandbox.org are unblocked. Khan Academy is a 501(c)(3) nonprofit organization. With RNA being a single-stranded nucleic acid subject to degradation, increases to mRNA stability will improve rates of translation while destructive targeting by small regulatory RNA (microRNAs or miRNAs) will decrease translation. Practice Exam 2 B/B Section Passage 1 Question 1. In comparison to transcriptional regulation, it results in much more immediate cellular adjustment through direct regulation of protein concentration. In eukaryotic cells like photoreceptors, gene expression is often controlled primarily at the level of transcription. FASEB J 10:453–60. All cells control or regulate Level up on all the skills in this unit and collect up to 700 Mastery points. Translational regulation refers to the control of the levels of protein synthesized from its mRNA. This involves the removal of introns that do not code for protein. Regulation after transcription Alternative splicing, miRNAs and siRNAs, translation initiation factors, & protein modifications. Khan Academy. Khan Academy. This regulation is vastly important to the cellular response to stressors, growth cues, and differentiation. After being pro­duced, the sta­bil­ity and dis­tri­b­u­tion of the dif­fer­ent tran­scripts is reg­u­lated (post-tran­scrip­tional reg­u­la­tion) by means of RNA bind­ing pro­tein (RBP) that con­trol the var­i­ous steps and rates cripts: events such as al­ter­na­tive splic­ing, nu­clear degra­da­tion (ex­o­some), pro­cess­ing, nu­clear ex­port (three al­ter­na­tive path­ways), se­ques­tra­tion in P-bod­ies for stor­age or degra­da­tion and ul­ti­mately trans­la­tion. As with the epigenetic and transcriptional stages of processing, this post-transcriptional step can also be regulated to control gene expression in the cell. If you're behind a web filter, please make sure that the domains *.kastatic.org and *.kasandbox.org are unblocked. Our mission is to provide a free, world-class education to anyone, anywhere. The micro RNA is a small RNA that does not code for proteins but is involved in the post-transcriptional regulation of gene expression and silencing of RNA. Section Bank B/B Section Passage 12 Question 96. Curr Opin Chem Biol 8:33–41. News; These pro­teins achieve these events thanks to a RNA recog­ni­tion motif (RRM) that binds a s… Myelogenous leukemia and two chemotherapeutic agents MCAT Official Prep (AAMC) Biology Question Pack, Vol. Donate or volunteer today! View Khan Academy MCAT Preview.pdf from BIOL MISC at Saint Louis University. If you're seeing this message, it means we're having trouble loading external resources on our website. Section Bank B/B Section Passage 9 Question 65. Site Navigation. This processing after an RNA molecule has been transcribed, but before it is translated into a protein, is called post-transcriptional modification. For instance, a photoreceptor cell in your eye can detect light because it expresses genes for light-sensitive proteins, as well as as genes for neurotransmitters that allow signals to be relayed to the brain. Google Classroom Facebook Twitter Donate or volunteer today! Please try again later. Sample Test B/B Section Passage 3 Question 14 Key Points • Catabolite activator protein (CAP) must bind to cAMP to activate transcription of the lac operon by RNA polymerase. Post-transcriptional control, basic concept of splicing (introns, exons) Regulation of chromatin structure Role of non-coding RNAs Our investigations span RNA stability (Giraldez, A et al. Biology is brought to you with support from the Amgen Foundation. To log in and use all the features of Khan Academy, please enable JavaScript in your browser. If the RNA is not processed, shuttled, or translated, then no protein will be synthesized. The big picture of eukaryotic gene regulation. Jensen ON (2004) Modification-specific proteomics: Characterization of post-translational modifications by mass spectrometry. Nuclear run-on assays indicated transcriptional regulation of MUC4 while no post-transcriptional mRNA stabilization was observed by actinomycin D chase experiments. RNAi is becoming an important method for analyzing … Pongali Raghavendra, Thammineni Pullaiah, in Advances in Cell and Molecular Diagnostics, 2018. Eukaryotic gene transcription: Going from DNA to mRNA, Practice: Transcription and RNA processing, let's talk about post transcriptional regulation which is regulation basically once DNA has been transcribed into mRNA and I've drawn out this little schematic for you here and it kind of just shows you how a DNA strand has corresponding RNA strand and then the mRNA strand afterwards and I'll sort of explain what all the different colors and words mean in just a little bit so once DNA is transcribed by RNA polymerase into the corresponding RNA strand this RNA strand needs to get what I call a tight a little haircut and then Don some protective outerwear before it can leave the comfort of the nucleus for its big debut into the cytoplasm in the form of a fully processed messenger RNA or mRNA strand now keep in mind that this form of regulation occurs in eukaryotes only and this modification also helps to stabilize the mRNA to protect it from premature degradation before it gets translated into a protein so as you can see here DNA gets transcribed one-to-one base for base into RNA and you can see here that there are sections of the RNA that ultimately make it into the finished mRNA these short segments which are termed exons and they are the sequences that code for the ultimate protein product and then there are short non-coding segments of RNA that get cut or spliced out and this would be the haircut that I alluded to earlier and so these are called introns and this is accomplished by a large molecular entity called the spliceosome so the spliceosome binds on either side of an intron loops the intron into a circle and then cleaves it off and then ly ate the two cut ends of the exposing exons together kind of cinches them together and an easy way to remember which sequences are exons which ones are introns is that exons exit the nucleus and introns stay in the nucleus so exons kind of stands for exit now even though the mRNA has gotten its nice little haircut it's not quite ready to leave the nucleus just yet it has to grab what is called a five prime cap and a 3 prime poly a tail now what are those things that I just mentioned so a five prime cap refers to changes at the five prime end of the mRNA and remember that this is the phosphate end of the nucleotide bases in the mRNA and some people like to remember this as F four five Prime and for the phosphate so that's how you can kind of keep the two end street and capping at the five prime end converts this end of the mRNA to a three prime end by a five prime to five prime linkage which basically just protects the mRNA from exonucleases which degrade foreign RNA the cap also promotes ribosomal binding for translation and also helps the regulation of nuclear export of the mRNA now the poly a tail that goes on the other end the three prime end of the mRNA which has the terminal hydroxyl group and so what do I mean when I say poly a tail well poly a tail refers to polyadenylation in which multiple adenosine monophosphate or basically an adenine bases are added to act as a buffer for exonucleases in order to increase the half-life of mRNA and again protect it from degradation and so the purpose of the poly a tail is really very similar to the five prime cap which is basically to protect from degradation help with promoting translation and regulating nuclear export the poly a tail also does one more thing and it kind of just helps with transcription termination for the RNA polymerase that's transcribing the messenger RNA polyadenylation is catalyzed by an enzyme called polyadenylate polymerase which adds the adenosine monophosphate using adenosine triphosphate as the substrate and the poly a tail is built until it's about 250 or so nucleotides long so overall the 5 prime cap and the poly a tail help to stabilize the mRNA for translation that's the key point to take home from here so once the mRNA has donned its cap and tail and had its introns sliced out it's now ready to exit the nucleus to be translated into a protein now additionally there is one more type of RNA regulation called RNA editing which is a process that results in sequence variation RNA molecule and is catalyzed by various enzymes RNA editing is relatively rare and these events may include insertion deletion and base substitution of nucleotides within the edited RNA molecule now one of these enzymes is called adenosine deaminase acting on RNA or ad a are enzymes which convert specific adenosine residues to inosine in an mrna molecule by hydrolytic deamination another type of editing is called site adine deaminase acting on RNA or c dar which involves deamination of cytosine to urine by site Adeem deaminase RNA editing is currently being extensively studied in relation to infectious diseases because the editing process alters viral enzymes and their function so kind of an exciting new emerging concept in post transcriptional regulation, Biology is brought to you with support from the Amgen Foundation. 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