Team:Hong Kong HKUST/riboregulator/regulatory RNAs catalog
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<p>asRNAs are single stranded RNAs that usually form base pair extensively with the target sense RNA / DNA. RNAs belonging to this class are capable of blocking translation, interfering with transcription, or modulating RNA stability. A review by Thomason and Storz provided detailed descriptions to their properties and functions.</p> | <p>asRNAs are single stranded RNAs that usually form base pair extensively with the target sense RNA / DNA. RNAs belonging to this class are capable of blocking translation, interfering with transcription, or modulating RNA stability. A review by Thomason and Storz provided detailed descriptions to their properties and functions.</p> | ||
<p><u>Reference:</u></p> | <p><u>Reference:</u></p> | ||
- | <p>Thomason MK, Storz G.,Bacterial antisense RNAs: how many are there, and what are they doing?Annual Review of Genetics Vol 44:167±188(2010)</p> | + | <p> Thomason MK, Storz G.,Bacterial antisense RNAs: how many are there, and what are they doing?, Annual Review of Genetics Vol 44:167±188(2010)</p> |
</div> | </div> |
Revision as of 23:29, 17 October 2014
Catalog for regulatory RNAs
(The page was created as part of iGEM 2014 HKUST team's effort in "Project Riboregulator" to catalog existing regulatory RNAs. Over the years, the number of regulatory RNAs in Part Registry has steadily increased over time and many has been made available to end users. Based on different mode actions and natures of regulatory RNAs, they can be grouped into different categories. However, the Part Registry currently does not have a catalog page, categorizing methods or guidelines to organize and curate existing regulatory RNAs. Some of them are grouped under type "RNA", while others are not. This is not useful for looking up and utilizing them.
We would like to solve this problem by designing a list of category tags as well as a guideline, so that automated display of regulatory RNAs by the <parttable> function can be facilitated. By doing so, we hope that we can assist other users to find and use those parts efficiently.
This page was written in compliance with Part Registry's format for general Catalog Pages. Currently, the information is uploaded manually because we have yet to submit our suggestions to iGEM HQ. Upon approval, we will tag existing regulatory RNAs and complete the page. Being part of the cross-cohort "Project Riboregulator", the page is far from complete and is expected to take shape by Spring 2015. We welcome and encourage constant update and adoption of this page in the future.)
Guideline for adding Categories
Some guidelines for categorizing RNA devices under this scheme:
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Riboregulator
Riboregulators regulate translation by having two elements, a cis-repressive sequence upstream of RBS in mRNA, and a non-coding RNA device, called trans-activating RNA. The cis-repressive sequence will binds to the 5'UTR, including the RBS by Watson-Crick base pairing, the sequestration of RBS represses translation. While trans-activating RNA will form complementary bases to cis-repressive sequence and exposing RBS for ribosomal binding and allow translation.
Proposed Categories: /RNA/non_coding/post_transcriptional/Riboregulator
Designer | Part Number | Description |
---|---|---|
Delft 2009 | BBa_K175029 | Weak lock |
Delft 2009 | BBa_K175030 | Key for lcok of weak RBS |
Delft 2009 | BBa_K175030 | Medium lock |
Delft 2009 | BBa_K175030 | Key for Medium lock |
Delft 2009 | BBa_K175034 | (Constitutive expression of GFP with weak RBS lock and inducible production of key for the lock Composite of K175029 + K175030 |
Delft 2009 | BBa_K175034 | Constitutive expression of GFP with medium RBS lock and inducible production of key for the lock Composite of K175031 + K175032 |
Caltech 2007 | BBa_I759015 | cis3-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759016 | cis4-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759020 | cis8-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759027 | cis3-repressed, tet-regulated Q |
Caltech 2007 | BBa_I759028 | cis4-repressed, tet-regulated Q |
Caltech 2007 | BBa_I759014 | (cis2-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759017 | cis5-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759018 | cis6-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759019 | cis7-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759013 | cis1-repressed, tet-regulated YFP |
Caltech 2007 | BBa_I759032 | Ptet_cis1_YFP |
Caltech 2007 | BBa_I759034 | Ptet_cis2_YFP |
Caltech 2007 | BBa_I759036 | Ptet_cis3_YFP |
Caltech 2007 | BBa_I759038 | Ptet_cis4_YFP |
Caltech 2007 | BBa_I759040 | Ptet_cis5_YFP |
Caltech 2007 | BBa_I759042 | Ptet_cis6_YFP |
Caltech 2007 | BBa_I759044 | Ptet_cis7_YFP |
Caltech 2007 | BBa_I759046 | Ptet_cis8_YFP |
Caltech 2007 | BBa_I759023 | pBAD-trans2 |
Caltech 2007 | BBa_I759022 | pBAD-trans1 |
Caltech 2007 | BBa_I759024 | pBAD-trans3 |
Caltech 2007 | BBa_I759025 | pBAD-trans4 |
Caltech 2007 | BBa_I759026 | pBAD-trans5 |
Peking 2007 | BBa_I714070 | R0040-J23078-pTet-Lock3 |
Peking 2007 | BBa_I714080 | [R0040][J23078][E0040][B0015] |
Peking 2007 | BBa_I714081 | R0040-J01010-E0040-B0015 |
Peking 2007 | BBa_I714037 | R751+ C600 E.coli cells with traI-R751 knockout |
Peking 2007 | BBa_I714074 | R0010-J23066-pLac-Key3-DblTerm Uses Lock and Key 3 from berkeley |
K.U. Leuven 2008 | BBa_K145215 | FILTER Key (TetR promoter + key) |
K.U. Leuven 2008 | BBa_K145216 | FILTER T7 RNA pol Lock from berkeley |
K.U. Leuven 2008 | BBa_K145217 | FILTER Complete The two previous together |
K.U. Leuven 2008 | BBa_K145220 | INVERTED TIMER |
K.U. Leuven 2008 | BBa_K145225 | RESET lactonase |
K.U. Leuven 2008 | BBa_K145300 | Lactonase controlled by key/lock |
K.U. Leuven 2008 | BBa_K145301 | lacI controlled by key/lock |
K.U. Leuven 2008 | BBa_K145302 | luxI generator controlled by key/lock |
K.U. Leuven 2008 | BBa_K145303 | GFP generator controlled by key/lock |
K.U. Leuven 2008 | BBa_K145003 | T7 PoPS -> RiboKey 3d |
K.U. Leuven 2008 | BBa_K145004 | T7 PoPS + RiboLock |> LuxI |
K.U. Leuven 2008 | BBa_K145005 | T7 PoPS + PR -> cI |
K.U. Leuven 2008 | BBa_K145216 | FILTER T7 RNA pol |
K.U. Leuven 2008 | BBa_K145251 | OLD RESET lactonase |
K.U. Leuven 2008 | BBa_K145253 | OLD INVERTIMER Part 1 |
K.U. Leuven 2008 | BBa_K145255 | NEW INVERTIMER part 1 |
K.U. Leuven 2008 | BBa_K145264 | test FILTER (new) |
K.U. Leuven 2008 | BBa_K145265 | test FILTER (old) |
K.U. Leuven 2008 | BBa_K145271 | GFP regulated by AND-gate |
K.U. Leuven 2008 | BBa_K145272 | GFP regulated by AND-gate |
K.U. Leuven 2008 | BBa_K145275 | T7 polymerase generator under TetR repressible promoter (filter) |
K.U. Leuven 2008 | BBa_K145276 | T7 polymerase generator under TetR repressible promoter |
K.U. Leuven 2008 | BBa_K145277 | T7 DNA polymerase regulated by lock |
K.U. Leuven 2008 | BBa_K145278 | T7 DNA polymerase regulated by [lock3d] |
K.U. Leuven 2009 | BBa_K238004 | Vanillin synthesis |
K.U. Leuven 2009 | BBa_K238006 | Short version of vanillin synthesis |
K.U. Leuven 2009 | BBa_K238012 | short version II of vanillin synthesis |
Groningen 2011 | BBa_K607005 | short version II of vanillin synthesis |
Groningen 2011 | BBa_K607000 | PhybB_taRNA |
VictoriaBC 2009 | BBa_K235010 | [K145303] (ribokey-controlled GFP generator) |
VictoriaBC 2009 | BBa_K235000 | [R0010][J23066] (pLac+ribokey+stop) |
VictoriaBC 2009 | BBa_K235001 | [J23102][J23066] (constitutive promoter+ribokey+stop) |
VictoriaBC 2009 | BBa_K235009 | [J23102][J23032] (constitutive promoter+ribolocked RBS) |
VictoriaBC 2009 | BBa_K235011 | [K235009][K235005] (ribokey-controlled mCherry generator) |
VictoriaBC 2009 | BBa_K235013 | [K145303][K235000] (ribokey-mediated pLac-controlled GFP reporter) |
VictoriaBC 2009 | BBa_K235014 | [K145303][K235001] (ribokey-mediated GFP generator) |
VictoriaBC 2009 | BBa_K235016 | [I0500][J23032] (pAra+ribolocked RBS) |
VictoriaBC 2009 | BBa_K235019 | [K235016][K235003] (ribokey-mediated pAra-controlled lambda repressor generator) |
VictoriaBC 2009 | BBa_K235021 | [K235009][K235003] (ribokey-mediated lambda repressor generator) |
VictoriaBC 2009 | BBa_K235022 | [K235018][K235019] (mCherry generator, pAra-controlled ribokey-mediated signal inversion) |
VictoriaBC 2009 | BBa_K235024 | [K235018][K235021] (mCherry generator, ribokey-mediated signal inversion) |
VictoriaBC 2009 | BBa_K235025 | [K235022][K235000] (NAND gate, pAra and pLac input signal control, mCherry output signal) |
VictoriaBC 2009 | BBa_K235026 | [K235022][K235001] (NAND gate control test, pLac positive control) |
VictoriaBC 2009 | BBa_K235027 | [K235024][K235000] (NAND gate control test, arabinose positive control) |
VictoriaBC 2009 | BBa_K235028 | [K235024][K235001] (NAND gate control test, positive control) |
Melborne2008 | BBa_K085000 | (lacI)promoter->key3c |
Melborne2008 | BBa_K085002 | pTet->lock3d->GFP |
Calgary 2007 | BBa_I737003 | OmpF controlled RNA Key |
Calgary 2007 | BBa_I737006 | Temperature induced repression/activation of an RNA key |
Calgary 2007 | BBa_I737005 | AHL and RNA lock controlled AraC |
RNA Aptamer
A RNA apatamer is any RNA molecule that can fold into a tertiary confirmation that binds with strong affinity and high specificity to small molecules through non-Watson-Crick base pairing.
Designer | Part Number | Description |
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Riboswitch
A riboswitch is a segment on mRNA that has the ability to detect small molecules or temperature, and regulates gene expression in an on or off manner. Riboswitches usually contain sensor domain for binding of small molecules and a regulatory domain for gene regulation. Riboswitches are therefore also aptamers in nature. Upon binding of a suitable ligand in the sensor domain, riboswitches undergo confirmation changes that can lead to different outcomes like translation inhibition or mRNA degradation.
Designer | Part Number | Description |
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RNA-IN-RNA-OUT
RNA-OUT is a small non-coding RNA that works at RNA level . RNA-OUT will bind to 5'UTR, which include RBS, of mRNA and prevents ribosome from binding to mRNA to inhibit translation of downstream gene. RNA-IN is also a non-coding RNA that is antisense to RNA-OUT and the binding of RNA-IN and RNA-OUT will prevent RNA-OUT from binding to mRNA, thus allowing ribosome to bind to mRNA and initiate translation.
Designer | Part Number | Description |
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Antisense RNAs (asRNAs)
asRNAs are single stranded RNAs that usually form base pair extensively with the target sense RNA / DNA. RNAs belonging to this class are capable of blocking translation, interfering with transcription, or modulating RNA stability. A review by Thomason and Storz provided detailed descriptions to their properties and functions.
Reference:
Thomason MK, Storz G.,Bacterial antisense RNAs: how many are there, and what are they doing?, Annual Review of Genetics Vol 44:167±188(2010)
Designer | Part Number | Description |
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Small interfering RNAs (siRNAs)
siRNAs work in the RNA interference (RNAi) pathway. siRNAs are usually produced by "dicing" exogenous, long double stranded RNA into 21-nucleotides small fragments. The siRNAs will then bind to Argonaute in RNA-induced silencing complex (RISC) and one strand is discarded. The remaining strand then guides the RISC to RNA targets with complementary base pairs and in most cases degrades the latter, result in inhibition of gene expression.
Designer | Part Number | Description |
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microRNAs (miRNAs)
miRNAs, like siRNA, work through the RNA interference (RNAi) pathway They are usually 19-25nt single stranded RNA that have an endogenous origin. They started as hairpin transcripts and processed by Drosha in non-random manner and are then processed by Dicer. Following binding to RISC, they regulate normal biological processes by degrading or inhibiting mRNAs that it has complementarity to.
Designer | Part Number | Description |
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Single guiding RNA (sgRNAs)
sgRNAs work in the CRISPR/Cas system. They are constructed by fusing functional domains of CRISPR RNA (crRNA) and trans-acting crRNA (taRNA) together through RNA linkers. They associate with Cas9 proteiens or their derivatives and guide them to DNA with complementarity with the targeting sequence of crRNA.
Designer | Part Number | Description |
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Ribozyme
A ribozyme is a RNA molecule with intrinsic catalytic activity, that can catalyse conversion of substrate into a product.
Designer | Part Number | Description |
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Aptazymes
RNA aptazymes, as the name suggests, are RNAs that carry properties from both aptamers and ribozymes. They are capable of sensing small molecules. Upon activation by a ligand, they can trigger ribozyme-mediated cleavage.
Designer | Part Number | Description |
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Structural Scaffolds
These ncRNAs have multiple interaction domains concatenated into a single molecule so as to facilitate co-localization of functional modules.
Designer | Part Number | Description |
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pT181-RNAI
The pT181-RNAI is a special class of regulatory RNAs derived from elements in Staphylococcus aureus pathogenicity plasmid pT181. A specific 5’ UTR region would normally form an anti-termination loop. Upon interacting with a pT181-RNAI, a premature terminator loop 5’ to the CDS will form and result in early termination before the mRNA can be completely transcribed.
Designer | Part Number | Description |
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Stability Control Elements
This class of ncRNAs can help to stabilize or destabilize a RNA molecule, typically by giving rise to hairpin structures that block or facilitate access of ribonucleases to the RNA itself.
Designer | Part Number | Description |
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Complex
This category contains ncRNA with dual or more functions resulting from combining 2 or multiple natures / functions of existing ncRNAs.
Designer | Part Number | Description |
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Targeted Sequence
This category deals with segments of ncRNAs that serve as recognizable targets by other ncRNAs.
Designer | Part Number | Description |
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Others
ncRNAs not belonging to the any of the above categories are listed here.
Designer | Part Number | Description |
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Differentiation
siRNA VS miRNAsiRNA and miRNA are two very similar RNA devices. Both of them will be processed by Dicer and both of them will from a RISC complex to carry out their function. However there are substantial differences between the two. First, siRNA are 20 to 25 nucleotides long; while miRNAs are 19-25 nucleotides long. Second, siRNA usually fully complement with the target mRNA; while miRNA can be partially complement with target mRNA.As a result, siRNA usually target few mRNA while miRNA can target 250-500 different mRNAs. Last but not least, siRNAs usually stem from exogenous DNA; while miRNA usually stem from endogenous DNA. |
siRNA / miRNA VS asRNAasRNAs refers to single stranded RNAs that are complementary to mRNA. Although no specific length requirement is imposed on asRNAs, asRNAs usually refers to RNA with longer length by historical reason. Whereas siRNA refers to short double stranded RNAs that are 20-25 nt long; miRNA usually refers to single stranded RNA that are 19-25 nt long. asRNA form duplex with mRNA, which will blocks the access of ribosome to mRNA, also the duplex may be degraded by ribonuclease exist in the cell. Either functions of siRNA and miRNA depends on RISC. |
Structural scaffold VS Stability control elementsStructural scaffold refers to the folding of RNA, which has the ability to recruit various molecules, mostly proteins. Scaffold may stabilize RNA devices and therefore a scaffold can also be stability control elements. While stability control elements refers to any RNA devices that contribute to the stability of RNA devices. It is not limited to RNA scaffold. One example is poly A tail elements for mRNA, it contributes to the stability of mRNA, however it is not a loop. |
Case Study
Case one: Spinach Aptamer
JustificationFUNCTION OF PART : //RNA/ncRNA/function/reporter
LEVEL OF REGULATION: NONE
CHASSIS: //Chassis/prokaryote/ecoli & //Chassis/eukaryote/human
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Case two: RNA_OUT
JustificationFUNCTION OF PART : //RNA/ncRNA/function/regulation
LEVEL OF REGULATION://RNA/ncRNA/function/regulation/RNA_level
NATURE OF PART: //RNA/ncRNA/RNA_OUT_type/ RNA_OUT
NATURE OF PART: //RNA/ncRNA/asRNA
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