Difference between revisions of "Part:BBa K3351011"
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<partinfo>BBa_K3351011 short</partinfo> | <partinfo>BBa_K3351011 short</partinfo> | ||
− | + | ===Summary=== | |
+ | Terminator regions, which are located downstream of protein coding sequences, encode 3′ untranslated regions (3′-UTRs) of mRNA. Terminator regions are usually involved in two complex events: ″transcriptional termination″, which involves the cleavage of 3′-mRNA and poly(A) addition and ″post-transcriptional regulation″, in which the 3′-UTR determines the stability, translational efficiency, and localization of the mRNA. Sequence and structural cis-elements located in the 3′-UTR of mRNA transcripts interact with RNA-binding proteins (RBPs) to post-transcriptionally regulate various aspects of gene expression including mRNA localization, translation, and decay. | ||
+ | |||
+ | ===Reference=== | ||
+ | [1] Richard, P. and Manley, J. L. (2009) Transcription termination by nuclear RNA polymerases Genes Dev. 23, 1247– 1269 | ||
+ | [2] Kuehner, J. N., Pearson, E. L., and Moore, C. (2011) Unravelling the means to an end: RNA polymerase II transcription termination Nat. Rev. Mol. Cell. Biol. 12, 283– 294 | ||
+ | [3] Kuersten, S. and Goodwin, E. B. (2003) The power of the 3′ UTR: translational control and development Nat. Rev. Genet. 4, 626– 637 | ||
+ | [4] Yamanishi, M., Ito, Y., Kintaka, R., Imamura, C., Katahira, S., Ikeuchi, A., Moriya, H., & Matsuyama, T. (2013). A genome-wide activity assessment of terminator regions in saccharomyces cerevisiae provides a "terminatome" toolbox. ACS Synthetic Biology, 2(6), 337-347. | ||
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Revision as of 13:51, 19 October 2020
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A T7 terminator of pet28a plasmid. SummaryTerminator regions, which are located downstream of protein coding sequences, encode 3′ untranslated regions (3′-UTRs) of mRNA. Terminator regions are usually involved in two complex events: ″transcriptional termination″, which involves the cleavage of 3′-mRNA and poly(A) addition and ″post-transcriptional regulation″, in which the 3′-UTR determines the stability, translational efficiency, and localization of the mRNA. Sequence and structural cis-elements located in the 3′-UTR of mRNA transcripts interact with RNA-binding proteins (RBPs) to post-transcriptionally regulate various aspects of gene expression including mRNA localization, translation, and decay.
Reference[1] Richard, P. and Manley, J. L. (2009) Transcription termination by nuclear RNA polymerases Genes Dev. 23, 1247– 1269 [2] Kuehner, J. N., Pearson, E. L., and Moore, C. (2011) Unravelling the means to an end: RNA polymerase II transcription termination Nat. Rev. Mol. Cell. Biol. 12, 283– 294 [3] Kuersten, S. and Goodwin, E. B. (2003) The power of the 3′ UTR: translational control and development Nat. Rev. Genet. 4, 626– 637 [4] Yamanishi, M., Ito, Y., Kintaka, R., Imamura, C., Katahira, S., Ikeuchi, A., Moriya, H., & Matsuyama, T. (2013). A genome-wide activity assessment of terminator regions in saccharomyces cerevisiae provides a "terminatome" toolbox. ACS Synthetic Biology, 2(6), 337-347. |
Secondary Structure
Measurement
- [http://openwetware.org/wiki/Cconboy:Terminator_Characterization/Results How these parts were measured]