Team:Hong Kong HKUST/riboregulator/regulatory RNAs catalog
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<tr><td>FUNCTION OF PART</td><td>//RNA/ncRNA/function/regulation</td></tr> | <tr><td>FUNCTION OF PART</td><td>//RNA/ncRNA/function/regulation</td></tr> | ||
<tr><td>NATURE OF PART</td><td>//RNA/ncRNA/aptamer</td></tr> | <tr><td>NATURE OF PART</td><td>//RNA/ncRNA/aptamer</td></tr> | ||
- | <tr><td | + | <tr><td rowspan="2">Chassis</td><td>//Chassis/prokaryote/ecoli</td></tr> |
<tr><td>//Chassis/eukaryote/human</td></tr> | <tr><td>//Chassis/eukaryote/human</td></tr> | ||
<tr><td> </td><td> </td></tr> | <tr><td> </td><td> </td></tr> |
Revision as of 21:36, 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.)
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
Part number | Description | Designer |
---|---|---|
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 |
Riboswitch
A riboswitch is a segment on mRNA that have the ability to detect small molecules or temperature, and regulate gene expression in on or off manner. Riboswitches usually contain a region for binding of small molecules, as known as sensor domain, and a region for gene regulation, as known as regulatory domain.In the presence of suitable ligand in the sensor domain, the structure of riboswitch will change. This change in conformation of riboswitch may give various action including translation inhibition or mRNA degradation.
Part number | Description | Designer |
---|
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.
Part number | Description | Designer |
---|
Small interfering RNAs (siRNAs)
siRNAs usually involved in RNA interference pathway. siRNA s are produced by "dicing" long double stranded RNA into 21-nucleotides small fragments. The siRNAs will then bind to a protein and one strand of siRNA is removed. Then siRNA, which have complementary base pairs with its target mRNA, will binds to target mRNA. The binding of siRNA usually causes the degradation of target mRNA, result in inhibition of gene expression.
Part number | Description | Designer |
---|
Single guiding RNA (sgRNAs)
sgRNAs are non-coding RNA that have a hairpin structure mimicking trans-acting RNA and crRNA in CRISPR system. When in complex with Cas9 the,complex are able to target specific DNA sequence and breaking double stranded DNA.
Part number | Description | Designer |
---|
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 antisense RNAAntisense RNAs refers to single stranded RNAs that are complementary to mRNA. Although no specific length requirement is imposed on antisense RNA, antisense RNA 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. Antisense RNA 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
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