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In the context of translation, a termination signal is the stop codon on the mRNA that elicits the release of the growing peptide from the ribosome. [ 2 ] Termination signals play an important role in regulating gene expression since they mark the end of a gene transcript and determine which DNA sequences are expressed in the cell. [ 1 ]
Translation is one of the key energy consumers in cells, hence it is strictly regulated. Numerous mechanisms have evolved that control and regulate translation in eukaryotes as well as prokaryotes. Regulation of translation can impact the global rate of protein synthesis which is closely coupled to the metabolic and proliferative state of a cell.
Poly-A polymerase adds approximately 200 adenines to the cleaved 3’ end of the RNA without a template. [35] The long poly-A tail is unique to transcripts made by Pol II. In the process of terminating transcription by Pol I and Pol II, the elongation complex does not dissolve immediately after the RNA is cleaved.
In biology, translation is the process in living cells in which proteins are produced using RNA molecules as templates. The generated protein is a sequence of amino acids . This sequence is determined by the sequence of nucleotides in the RNA.
Translation ends with a stop codon which may be a UAA, UGA, or UAG triplet. The mRNA does not contain all the information for specifying the nature of the mature protein. The nascent polypeptide chain released from the ribosome commonly requires additional processing before the final product emerges.
Once the polymerase nears the end of the gene it is transcribing, it encounters a series of G nucleotides which causes it to stall. [1] This stalling allows the rho factor to catch up to the RNA polymerase. The rho protein then pulls the RNA transcript from the DNA template and the newly synthesized mRNA is released, ending transcription.
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Translation promotes transcription elongation and regulates transcription termination. Functional coupling between transcription and translation is caused by direct physical interactions between the ribosome and RNA polymerase ("expressome complex"), ribosome-dependent changes to nascent mRNA secondary structure which affect RNA polymerase activity (e.g. "attenuation"), and ribosome-dependent ...