Team:Valencia/Parts

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Submitted Biobricks
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==Parts==
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We placed the first prion-based inheritance element construction into a ''standard biological parts'', also called ''BioBricks''. These are nucleic acid coding molecular biological functions, along with the associated information defining and describing the parts.
 +
You can find more information about this on the website of [http://biobricks.org/ The BioBricks Foundation].
 +
 +
Using these molecules any synthetic biologist or biological engineer can program living organisms. All our parts are available to anyone for free via MIT's [http://partsregistry.org Registry of Standard Biological Parts].
 +
 +
We also placed the PM2 gene, coding the LEA3 protein, in another Biobrick, and probed that it conferes to our ''E. coli'' protection against extreme temperature.
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<groupparts>iGEM010 Valencia</groupparts>
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== '''LEA''' ==
 +
 +
 +
=== Function ===
 +
 +
PM2 corresponds to the LEA3 protein from soybean (''Glycine max''). Late Embryogenesis Abundant (LEA) proteins are known for their roles in plant embryogenesis, as important dessication-resistance factors. It has also been shown that they confer tolerance under several stress conditions in ''Escherichia coli''. You can read more about it in our wiki and in several references, as, for example, the following: Liu ''et al.'' (2010).
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Biobricks Submitted</span></center>
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<div class="thumbcaption"><b>LEA14</b> Three dimensional representation of the LEA14 proteinn.(EPDB)</div></div></div></div>
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===Parts===
 
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New for iGEM 2010 is the ''groupparts'' tag.  This tag will generate a table with all of the parts that your team adds to your team sandbox.  Note that if you want to document a part you need to document it on the [http://partsregistry.org Registry], not on your team wiki.
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PM2 can be useful as a general stress-resistance factor. It could improve survival under low or high temperatures, water stress and maybe other atypical conditions.
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<groupparts>iGEM010 Valencia</groupparts>
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===Original source===
 +
Our PM2 was inserted into the pET28a vector and transformed into ''E. coli'' BL21 Star cells.
 +
We sincerely thank professor Yizhi Zheng and Yun Liu (College of Life Science, Shenzhen University. Guangdong, China) for sending us the plasmid with the gene, and, in consequence, let us develop our project.
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== '''LEA''' ==
 
-
The LEA fragment we used was kindly sent by Liu (?) and consists of the protein PM2 (LEA3) from soybean (Glycine max (L) Merr.). It was inserted into the pET28a vector and transformed into E. coli BL21 Star cells. In order to amplificate it and clone it into the pSB1C3, we used the forward primer actagtagcggccgctgcagATGGCGTCCAAGAAAC and the reverse primer tctagaagcggccgcgaattcTGCGTCTATATATAC (capital letters indicate the region of the sequence that pairs with the coding sequence of PM2).
+
===Sequence===
 +
 
 +
The amplification previous to the clonation into the pSB1C3, was made using the primers previously employed in Liu and Zheng (2005):
 +
* Forward actagtagcggccgctgcagATGGCGTCCAAGAAAC
 +
* Reverse tctagaagcggccgcgaattcTGCGTCTATATATAC
 +
(capital letters indicate the region of the sequence that pairs with the coding sequence of PM2).
 +
 
 +
The sequence of the part, the  PM2 gene, was first reported by Z.-Y. Chen, .Y-I.C. Hsing and T.-Y. Chow and it is available at the NCBI Nucleotide database (accession number AF532313). The complete sequence is pasted below:
 +
 
 +
        1 cacaaaagtg ttccacttga gtgaaaagta gtgtgttaag aactaaacaa tttttcaatg
 +
      61 gcgtccaaga aacaagagga gcgagctgag gcagctgcga aagttgctgc caaagaactc
 +
      121 gaacaagtca acagagaaag aagagaccgt gatttcggtg ttgttgctga acaacaacaa
 +
      181 caacatcatc aggaagatca acaaaaacgt ggtgtaatcg ggtccatgtt taaggcggtg
 +
      241 caagacacct acgagaacgc caaggaagct gtcgttggca agaaagaagc tactaataac
 +
      301 gcgtacagta atacagaggt tattcacgat gttaacattc agcccgatga cgtgtcggca
 +
      361 acgggggaag taagggacat atcagccaca aagactcatg atatctacga ttctgccacg
 +
      421 gacaacaaca acaacaaaac cggttccaag gtcggagagt acgcagatta cgcttctcag
 +
      481 aaggccaagg aaacaaaaga tgcaacgatg gaaaaagctg gagagtacac agattatgct
 +
      541 tcgcagaaag cgaaggaagc gaagaagacg accatggaga agggtggaga atacaaggat
 +
      601 tactctgcgg agaaagctaa ggagagaaaa gatgctactg tgaataagat gggagagtat
 +
      661 aaggactatg ctgcggagaa agccaaagag gggaaagatg ctactgtgaa taaaatggga
 +
      721 gagtataagg actatgctgc ggagaaaacg aaagagggga aagatgccac tgtgaataag
 +
      781 atgggagagt ataaggatta cactgcggag aaggcgaaag aggggaaaga tacgacgttg
 +
      841 gggaagcttg gggagctgaa ggacacggct tcggatgcgg cgaagagggc cgtgggttac
 +
      901 ttgagcggca agaaagagga aactaaagag atggcttcgg agaccgccga ggcgacggcg
 +
      961 aataaggcag gggagatgaa ggaggcaaca aagaaaaaga cggcggagac cgcggaggcg
 +
    1021 gcgaagaata aggcggggga gatcaaggac agagccgcgg agacggcgga ggccgcgaaa
 +
    1081 aacaagaccg cggagaccgc ggaagtgacg aagaataagg ctttggagat gaaggatgca
 +
    1141 gcgaaggaca ggaccgctga gacaacggat gcggcgaagc agaaaactgc acaggcaaag
 +
    1201 gagaacacca aggaaaatgt gagtggtgca ggtgaaactg caaggaggaa aatggaagag
 +
    1261 ccaaagcttc aaggtaaaga agggtatggg ggccgtggag acaaggtggt ggtgaaagtg
 +
    1321 gaagagagtc gaccaggggc aattgcggaa acgctgaaag ccgccgacca gattgcggga
 +
    1381 cagaccttca acgatgtagg acgcttcgat gaagagggtg tcgtcaatgt ggagcgccgc
 +
    1441 aagaaataat taaaacgtga tctatgatac aacaatatta gtatatatag acgcatgcag
 +
    1501 tttatatagt atatattgtc atgttgtatg tttttacatt ttggtttgct tgtttacatt
 +
    1561 ctcttcaaaa aaaaaaaaaa tgtgtagtac gtgtaaggtt ttgaagattg gttctaggct
 +
    1621 ccgtgggaac catttcaaca ataaacattt tgcgcgttct tgtacacgta gtgatgagaa
 +
    1681 gagatgcctt atgggcagta tcatctaaaa cttattttca tccatcatag aatttggatc
 +
    1741 t
 +
 
 +
== '''Prionic Switch''' ==
 +
 
 +
 
 +
===Components===
 +
The switch is formed by two different parts: the activator and the reporter. The activator part is a construction of two fragments: the NM domains of the protein Sup35, which confers to the protein the prionic activity, and the GR<sup>526</sup> portion, which contains the DNA-binding and transcription-activation domains. The ligand-binding domain of the protein GR was eliminated, decoupling the response of the protein to the presence of glucocorticoids, and thus generating a constitutive transcription activation factor. The normal activity of this protein results in the activation of the genes preceded by the GRE (Glucocorticoid Response Element). When exposed to heat shock or other stress conditions, the NM domains start the prionic activity, eventually inhibiting the activation of transcription.
 +
 
 +
This part was amplified by using the primers indicated by Li and Lindquist (2000), together with the sequence recommended to use for the ligation protocol with the plasmid pSB1C3. Those primers are:
 +
* Forward actagtagcggccgctgcagATGTCGGATTCAAAC
 +
* Reverse tctagaagcggccgcgaattcTCCTGCAGTGGCTTG
 +
(again, capital letters represent the region that pairs with the coding sequence of NMGR<sup>526</sup>).
 +
 
 +
The second part consists of the GRE followed by the reporter gene. In our experiments, we used LacZ for this purpose. The amplification of this part could not be made because of some problems found when trying to find the sequence of the GRE.
 +
 
 +
===Sequence===
 +
The sequence of NMGR<sup>526</sup> can be reconstructed from the separated parts that compose it. The NM domain sequence can be found in the SUP35/YDR172W first fragments. The GR<sup>526</sup> sequence comes from the nucleotides 14-2398 of the NM_012576 (GI:158303299) locus. The sequence of the part is shown below:
 +
 
 +
    1 atgtcggattcaaaccaaggcaacaatcagcaaaactaccagcaatacagccagaacggt
 +
  61 aaccaacaacaaggtaacaacagataccaaggttatcaagcttacaatgctcaagcccaa
 +
  121 cctgcaggtgggtactaccaaaattaccaaggttattctgggtaccaacaaggtggctat
 +
  181 caacagtacaatcccgacgccggttaccagcaacagtataatcctcaaggaggctatcaa
 +
  241 cagtacaatcctcaaggcggttatcagcagcaattcaatccacaaggtggccgtggaaat
 +
  301 tacaaaaacttcaactacaataacaatttgcaaggatatcaagctggtttccaaccacag
 +
  361 tctcaaggtatgtctttgaacgactttcaaaagcaacaaaagcaggccgctcccaaacca
 +
  421 aagaagactttgaagcttgtctccagttccggtatcaagttggccaatgctaccaagaag
 +
  481 gttggcacaaaacctgccgaatctgataagaaagaggaagagaagtctgctgaaaccaaa
 +
  541 gaaccaactaaagagccaacaaaggtcgaagaaccagttaaaaaggaggagaaaccagtc
 +
  601 cagactgaagaaaagacggaggaaaaatcggaacttccaaaggtagaagaccttaaaatc
 +
  661 tctgaatcaacacataataccaacaatgccaatgttaccagtgctgatgccttgatcaag
 +
  721 gaacaggaagaagaagtggatgacgaagttgttaacgatatggactccaaagaatcctta
 +
  781 gctccccctggtagagacgaagtccctggcagtttgcttggccaggggagggggagcgta
 +
  841 atggacttttataaaagcctgaggggaggagctacagtcaaggtttctgcatcttcgccc
 +
  901 tcagtggctgctgcttctcaggcagattccaagcagcagaggattctccttgatttctcg
 +
  961 aaaggctccacaagcaatgtgcagcagcgacagcagcagcagcagcagcagcagcagcag
 +
1021 cagcagcagcagcagcagcagcagccagacttatccaaagccgtttcactgtccatgggg
 +
1081 ctgtatatgggagagacagaaacaaaagtgatggggaatgacttgggctacccacagcag
 +
1141 ggccaacttggcctttcctctggggaaacagactttcggcttctggaagaaagcattgca
 +
1201 aacctcaataggtcgaccagcgttccagagaaccccaagagttcaacgtctgcaactggg
 +
1261 tgtgctaccccgacagagaaggagtttcccaaaactcactcggatgcatcttcagaacag
 +
1341 aaaatcgaaaaagccagaccggcaccaacggaggcagtgtgaaattgtatcccacagacc
 +
1401 aaagcacctttgacctcttgaaggatttggagttttccgctgggtccccaggtaaagaca
 +
1461 caaacgagagtccctggagatcagacctgttgatagatgaaaacttgctttctcctttgg
 +
1521 cgggagaagatgatccattccttctcgaaggggacacgaatgaggattgtaagcctctta
 +
1581 ttttaccggacactaaacctaaaattaaggatactggagatacaatcttatcaagtccca
 +
1641 gcagtgtggcactgccccaagtgaaaacagaaaaagatgatttcattgaactttgcaccc
 +
1701 ccggggtaattaagcaagagaaactgggcccagtttattgtcaggcaagcttttctggga
 +
1761 caaatataattggtaataaaatgtctgccatttctgttcatggtgtgagtacctctggag
 +
1821 gacagatgtaccactatgacatgaatacagcatccctttctcagcagcaggatcagaagc
 +
1881 ctgtttttaatgtcattccaccaattcctgttggttctgaaaactggaataggtgccaag
 +
1941 gctccggagaggacagcctgacttccttgggggctctgaacttcccaggccggtcagtgt
 +
2001 tttctaatgggtactcaagccctggaatgagaccagatgtaagctctcctccatccagct
 +
2061 cgtcagcagccacgggaccacctcccaagctctgcctggtgtgctccgatgaagcttcag
 +
2121 gatgtcattacggggtgctgacatgtggaagctgcaaagtattctttaaaagagcagtgg
 +
2181 aaggacagcacaattacctttgtgctggaagaaacgattgcatcattgataaaattcgaa
 +
2241 ggaaaaactgcccagcatgccgctatcggaaatgtcttcaggctggaatgaaccttgaag
 +
2301 ctcgaaaaacaaagaaaaaaatcaaagggattcagcaagccactgcaggagtctca
 +
 
 +
 
 +
===Sup35p===
 +
[''PSI<sup>+</sup>''] is a non-Mendelian trait of ''Saccharomyces cerevisae'' that supress nonsense codons.  This phenotype is due to a self-replication conformation (prion state) of a protein encoded by the gene Sup35. This protein, Sup35p, is the yeast eukariotyc release factor 3 (eRF3) and forms the translation termination complex with Sup45p (eRF1). The function of Sup35p is releasing the nascent polypeptide chain from the ribosome through GTP hydrolysis when Sup45p recognize a stop codon (Shorter and Lindquist, 2005).
 +
 
 +
Sup35p is 685 amino acids long and has three distinct parts (Fig.2). The NH2-terminus (N) is termed the prion-forming domain (PrD) because plays a critical role in Sup35p’s changes in proteic conformation and it is responsible for its prion behaviour. This domain is 114 amino acids long and has a high content in glutamine and asparagine. The middle region (M) provides a solubilizing and/or spacing function. Finally, the COOH-terminus (C) is responsible for the translation-termination activity.
 +
 
 +
[[Image:Valencia_prion_sup35.jpg|thumb|center|400px|'''Figure 2'''. The prion domain of Sup35 is Q/N Rich and has the ability to propogate the corresponding prion in the absence of the rest of the molecule. Source: Wickner ''et al''. 2008.]]
 +
 
 +
In [''PSI<sup>+</sup>''] cells, most Sup35p is insoluble and nonfunctional, causing an increase in the translational read-through of stop codons. This trait is heritable because Sup35p in the amyloid state as every prion influences new Sup35p to adopt the same conformation and passes from mother cell to daughter. In [''psi<sup>-</sup>''] cells, the translation-termination factor Sup35p is soluble and functional.
 +
 
 +
===Behaviour===
 +
 
 +
Sup35p is a subunit of the translation termination complex. Its prionic nature has been proposed to have some effect on the stress response, as a possible mechanism to obtain modified genetic expression products. When the prionic conformation is activated, the termination of translation is less effective and thus new longer proteins form (True and Lindquist, 2000; Tyedmers ''et al.'', 2008). When the sequence corresponding to the NM domains of Sup35p is fused to other gene, the protein resulting of this construction acquires the prionic behaviour (Li and Lindquist, 2000).
 +
 
 +
On the other side, GR activates the transcription of genes preceded by GRE (Glucocorticoid Receptor Element) when steroid hormones are present (Heitzer ''et al.'', 2007). However, it becomes a constitutive transcription activator when it lacks its C terminal ligand-binding domain (Schena and Yamamoto, 1988). Because of the length of amino acids of the cut protein, this short version of GR is named GR<sup>526</sup>.
 +
 
 +
Li and Lindquist (2000) showed that the fused protein (NMGR<sup>526</sup>) is a functional constitutive transcription activator. In addition, when the prionic conformation is reached because of the presence of a certain stimulus, NMGR<sup>526</sup> is no longer capable of inducing the activation of the gene preceded by GRE. Tyedmers ''et al.'' (2000) checked the conditions that trigger the prionic conformation and they found that heat shock is a significantly relevant factor. The cells in which the prionic conformation is induced, the process is promoted in an autocatalytic manner and all the protein is found in the prionic conformation. The cells resulting show the phenotype [''PSI<sup>+</sup>''].
 +
 
 +
It is important to note that the rate of the change of conformation is not equal to zero even at optimal growth conditions, and that not all the cells become [''PSI<sup>+</sup>'']. The rate of spontaneous activation of the switch is thought to be around 10<sup>-6</sup> or 10<sup>-7</sup> (Alberti ''et al.'', 2009). This process is promoted under heat stress (Tyedmers ''et al.'', 2008), probably because of the important role of heat shock proteins like Hsp104 in the formation and maintenance of the amyloid fiber (Halfmann ''et al.'', 2009). These approximate rates will have very important implications for the yeastworld model that we briefly describe in the following subsection, and with more detail in our wiki [https://2010.igem.org/Team:Valencia/Modeling  Modeling] section.
 +
 
 +
 
 +
===Original source===
 +
 
 +
We thank D. Susan Lindquist (Whitehead Institute for Biomedical Research / Howard Hughes Medical Institute / Department of  Biology, MIT) for sending us the prionic system transformed E.coli strains.
 +
 
 +
 
 +
==Making our Biobricks==
 +
After a lot of attempts trying to make our BioBricks (we had some dificulties at different steps) we achieved our purpose: we built 2 BioBricks  and we sent them to de Registry.
 +
===PCR===
 +
First of all, we needed enough amounts of DNA in order to insert them as our Biobrick into the pSB1C3 provided by the Registry.
 +
We had purified DNA from PM2 E.coli strains and from NMGR526 E.coli strains. Using these as our DNA template we amplified the quoted genes: PM2 and NMGR526.
 +
The chosen program was:
 +
*A first denaturation cycle: 94ºC 3min
 +
*30 amplification cycles, made up of:
 +
**94ºC 30s
 +
**55ºC 1min
 +
**72ºC 1min
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*Final step: 72ºC 7min
 +
 
 +
===Digestion===
 +
Next step was the digestion of the amplified material with the enzimes EcoRI and PstI, keeping the reaction tubes during 4-5 hours at 37ºC with:
 +
 
 +
'''PM2'''
 +
*1 μL PstI
 +
*1μL EcoRI
 +
*2,5 μL of insert PM2 (at 370,9 ng/ μL)
 +
*4 μL H buffer
 +
*31,5 μL water
 +
 
 +
 
 +
'''NMGR<sup>526</sup>'''
 +
*1 μL PstI
 +
*1 μL EcoRI
 +
*1,8 μL of insert NMGR<sup>526</sup> (at 504,3 ng/ μL)
 +
*4 μL H buffer
 +
*32,2 μL water
 +
 
 +
===Ligation===
 +
After purificating the DNA using a simple etanol precipitation protocol, we resuspended the DNA into 12 μL of water. Then, we put both plasmid and PM2 in one tube, and both plasmid and NMGR526 in another one, using these amounts of components:
 +
*1 μL T4 ligase
 +
*3 μL pSB1C3
 +
*4 μL ligation buffer
 +
*Whole 12 μL of our DNA
 +
We kept it O/N in the fridge at 4ºC.
 +
 
 +
===Transformation===
 +
We transformed DH5α ''E.coli'' competent strain with our ligation product using a standard heat shock transformation protocol.
 +
 
 +
===Miniprep===
 +
Before the tranformation ending O/N step, we noticed that we had grown colonies in cloramphenicol LB plaques, so we used them to make a plasmidic DNA extraction (Miniprep: High Pure Plasmid Isolation Kit, Roche. 11 754 785 001).
 +
In order to check the process had been successful, we made an electrophoresis gel, putting  four careers:
 +
#Ligation product digested with EcoRI
 +
#Ligation product digested with PstI
 +
#Ligation product digested with EcoRI and PstI
 +
#Ligation product without any restriction enzyme
 +
 
 +
==References==
 +
*Alberti, S., Halfmann, R., King, O., Kapila, A., Lindquist, S. (2009). A systematic survey identifies prions and illuminates sequence features of prionogenic proteins. ''Cell''. 137: 146-158.
 +
 
 +
*Cobb, N.J., Surewicz, W. K. (2009). Prion diseases and their biochemical mechanisms. ''Biochemistry''. 48: 2574–2585.
 +
 
 +
*Cox,B.S. (1965). A cytoplasmic suppressor of super-suppressor in yeast. ''Heredity''. 20: 505–521.
 +
 
 +
*Halfmann, R., Alberti, S., Lindquist, S. (2009). Prions, protein homeostasis and phenotypic diversity. ''Trends in Cell Biology''. 20: 125-133.
 +
 
 +
*Heitzer, M.D., Wolf, I.M., Sanchez, E.R., Witchel, S.F., DeFranco, D.B. (2007). Glucocorticoid receptor phisiology. ''Rev. Endocr. Metab. Disord.''. 8: 321-330.
 +
 
 +
*Li, L., Lindquist, S. (2000). Creating a protein-based element of inheritance. ''Science''. 287: 661-664.
 +
 
 +
*Liu, Y., Zheng, Y. (2005). PM2, a group 3 LEA protein from soybean, and its 22-mer repeating region confer salt tolerance in Escherichia coli. ''Biochem. Biophys. Res. Com.'' 331: 325-332.
 +
 
 +
*Liu, Y., Zheng, Y., Zhang, Y., Wang, W., Li, R. (2010). Soybean PM2 protein (LEA3) confers the tolerance of ''Escherichia col''i and stabilization of enzyme activity under diverse stresses. ''Current Microbiology''. 60: 373-378.
 +
 
 +
*Prusiner, S.B. (1982). Novel proteinaceous infectious particles cause scrapie. Science. 216: 136–144.
 +
 
 +
*Prusiner, S.B. (1998). Prions. ''PNAS''. 95: 13363–13383.
 +
 
 +
*Si, K., Lindquist, S. Kandel, E.R. (2003). A neuronal isoform of the Aplysia CPEB has prion-like properties. ''Cell''. 115: 879-891.
 +
 
 +
*Schena, M., Yamamoto, K.R. (1988). Mammalian glucocorticoid receptor derivatives enhance transcription in yeast. ''Science''. 241: 965-967.
 +
 
 +
*Shorter, J., Lindquist, S. (2005). Prions as adaptive conduits of memory and inheritance. ''Nature''. 6: 435-450.
 +
 
 +
*True, H.L., Lindquist, S. (2000). A yeast prion provides a mechanism for genetic variation and phenotypic diversity. ''Nature''. 407: 477-483.
 +
 
 +
*Tyedmers, J., Madariaga, M.L., Lindquist, S. (2008). Prion switching in response to environmental stress. ''PLoS Biology''. 6: e294.
-
== PRIONIC SWITCH: ==
+
*Wickner, R.B. (1994). [URE3] as an altered ''URE2'' protein: evidence for a prion analog in ''Saccharomyces cerevisiae''. ''Science''. 264: 566-569.
-
The switch is formed by two different parts: the activator and the reporter. The activator part is a construction of two fragments: the NM domains of the protein Sup35, which confers to the protein the prionic activity, and the GR526 portion, which contains the DNA-binding and transcription-activation domains. The ligand-binding domain of the protein GR was eliminated, decoupling the response of the protein to the presence of glucocorticoids, and thus generating a constitutive transcription activation factor. The normal activity of this protein results in the activation of the genes preceded by the GRE (Glucocorticoid Response Element). When exposed to heat shock or other stress conditions, the NM domains start the prionic activity, eventually inhibiting the activation of transcription.
+
*Wickner, R.B., Shewmaker, F., Kryndushkin, D., Edskes, H.K. (2008). Protein inheritance (prions) based on parallel in-register β-sheet amyloid structures. ''BioEssays''. 30: 955-964.
-
This part was amplified by using the primers indicated by Lindquist et al (?), together with the sequence recommended to use for the ligation protocol with the plasmid pSB1C3. Those primers are: forward actagtagcggccgctgcagATGTCGGATTCAAAC and reverse tctagaagcggccgcgaattcTCCTGCAGTGGCTTG (again, capital letters represent the region that pairs with the coding sequence of NMGR526).
+
-
The reporter part consists of the GRE and the reporter gene. In our experiments, we used LacZ as a reporter. The amplification of this part could not be made because we had some trouble finding the sequence of the GRE.
+
</div>
</div>

Latest revision as of 16:23, 9 February 2011


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Submitted Biobricks

Parts

We placed the first prion-based inheritance element construction into a standard biological parts, also called BioBricks. These are nucleic acid coding molecular biological functions, along with the associated information defining and describing the parts. You can find more information about this on the website of The BioBricks Foundation.

Using these molecules any synthetic biologist or biological engineer can program living organisms. All our parts are available to anyone for free via MIT's Registry of Standard Biological Parts.

We also placed the PM2 gene, coding the LEA3 protein, in another Biobrick, and probed that it conferes to our E. coli protection against extreme temperature.

<groupparts>iGEM010 Valencia</groupparts>

LEA

Function

PM2 corresponds to the LEA3 protein from soybean (Glycine max). Late Embryogenesis Abundant (LEA) proteins are known for their roles in plant embryogenesis, as important dessication-resistance factors. It has also been shown that they confer tolerance under several stress conditions in Escherichia coli. You can read more about it in our wiki and in several references, as, for example, the following: Liu et al. (2010).

LEA14 Three dimensional representation of the LEA14 proteinn.(EPDB)


PM2 can be useful as a general stress-resistance factor. It could improve survival under low or high temperatures, water stress and maybe other atypical conditions.

Original source

Our PM2 was inserted into the pET28a vector and transformed into E. coli BL21 Star cells. We sincerely thank professor Yizhi Zheng and Yun Liu (College of Life Science, Shenzhen University. Guangdong, China) for sending us the plasmid with the gene, and, in consequence, let us develop our project.


Sequence

The amplification previous to the clonation into the pSB1C3, was made using the primers previously employed in Liu and Zheng (2005):

  • Forward actagtagcggccgctgcagATGGCGTCCAAGAAAC
  • Reverse tctagaagcggccgcgaattcTGCGTCTATATATAC

(capital letters indicate the region of the sequence that pairs with the coding sequence of PM2).

The sequence of the part, the PM2 gene, was first reported by Z.-Y. Chen, .Y-I.C. Hsing and T.-Y. Chow and it is available at the NCBI Nucleotide database (accession number AF532313). The complete sequence is pasted below:

       1 cacaaaagtg ttccacttga gtgaaaagta gtgtgttaag aactaaacaa tttttcaatg
      61 gcgtccaaga aacaagagga gcgagctgag gcagctgcga aagttgctgc caaagaactc
     121 gaacaagtca acagagaaag aagagaccgt gatttcggtg ttgttgctga acaacaacaa
     181 caacatcatc aggaagatca acaaaaacgt ggtgtaatcg ggtccatgtt taaggcggtg
     241 caagacacct acgagaacgc caaggaagct gtcgttggca agaaagaagc tactaataac
     301 gcgtacagta atacagaggt tattcacgat gttaacattc agcccgatga cgtgtcggca
     361 acgggggaag taagggacat atcagccaca aagactcatg atatctacga ttctgccacg
     421 gacaacaaca acaacaaaac cggttccaag gtcggagagt acgcagatta cgcttctcag
     481 aaggccaagg aaacaaaaga tgcaacgatg gaaaaagctg gagagtacac agattatgct
     541 tcgcagaaag cgaaggaagc gaagaagacg accatggaga agggtggaga atacaaggat
     601 tactctgcgg agaaagctaa ggagagaaaa gatgctactg tgaataagat gggagagtat
     661 aaggactatg ctgcggagaa agccaaagag gggaaagatg ctactgtgaa taaaatggga
     721 gagtataagg actatgctgc ggagaaaacg aaagagggga aagatgccac tgtgaataag
     781 atgggagagt ataaggatta cactgcggag aaggcgaaag aggggaaaga tacgacgttg
     841 gggaagcttg gggagctgaa ggacacggct tcggatgcgg cgaagagggc cgtgggttac
     901 ttgagcggca agaaagagga aactaaagag atggcttcgg agaccgccga ggcgacggcg
     961 aataaggcag gggagatgaa ggaggcaaca aagaaaaaga cggcggagac cgcggaggcg
    1021 gcgaagaata aggcggggga gatcaaggac agagccgcgg agacggcgga ggccgcgaaa
    1081 aacaagaccg cggagaccgc ggaagtgacg aagaataagg ctttggagat gaaggatgca
    1141 gcgaaggaca ggaccgctga gacaacggat gcggcgaagc agaaaactgc acaggcaaag
    1201 gagaacacca aggaaaatgt gagtggtgca ggtgaaactg caaggaggaa aatggaagag
    1261 ccaaagcttc aaggtaaaga agggtatggg ggccgtggag acaaggtggt ggtgaaagtg
    1321 gaagagagtc gaccaggggc aattgcggaa acgctgaaag ccgccgacca gattgcggga
    1381 cagaccttca acgatgtagg acgcttcgat gaagagggtg tcgtcaatgt ggagcgccgc
    1441 aagaaataat taaaacgtga tctatgatac aacaatatta gtatatatag acgcatgcag
    1501 tttatatagt atatattgtc atgttgtatg tttttacatt ttggtttgct tgtttacatt
    1561 ctcttcaaaa aaaaaaaaaa tgtgtagtac gtgtaaggtt ttgaagattg gttctaggct
    1621 ccgtgggaac catttcaaca ataaacattt tgcgcgttct tgtacacgta gtgatgagaa
    1681 gagatgcctt atgggcagta tcatctaaaa cttattttca tccatcatag aatttggatc
    1741 t

Prionic Switch

Components

The switch is formed by two different parts: the activator and the reporter. The activator part is a construction of two fragments: the NM domains of the protein Sup35, which confers to the protein the prionic activity, and the GR526 portion, which contains the DNA-binding and transcription-activation domains. The ligand-binding domain of the protein GR was eliminated, decoupling the response of the protein to the presence of glucocorticoids, and thus generating a constitutive transcription activation factor. The normal activity of this protein results in the activation of the genes preceded by the GRE (Glucocorticoid Response Element). When exposed to heat shock or other stress conditions, the NM domains start the prionic activity, eventually inhibiting the activation of transcription.

This part was amplified by using the primers indicated by Li and Lindquist (2000), together with the sequence recommended to use for the ligation protocol with the plasmid pSB1C3. Those primers are:

  • Forward actagtagcggccgctgcagATGTCGGATTCAAAC
  • Reverse tctagaagcggccgcgaattcTCCTGCAGTGGCTTG

(again, capital letters represent the region that pairs with the coding sequence of NMGR526).

The second part consists of the GRE followed by the reporter gene. In our experiments, we used LacZ for this purpose. The amplification of this part could not be made because of some problems found when trying to find the sequence of the GRE.

Sequence

The sequence of NMGR526 can be reconstructed from the separated parts that compose it. The NM domain sequence can be found in the SUP35/YDR172W first fragments. The GR526 sequence comes from the nucleotides 14-2398 of the NM_012576 (GI:158303299) locus. The sequence of the part is shown below:

   1 atgtcggattcaaaccaaggcaacaatcagcaaaactaccagcaatacagccagaacggt
  61 aaccaacaacaaggtaacaacagataccaaggttatcaagcttacaatgctcaagcccaa
 121 cctgcaggtgggtactaccaaaattaccaaggttattctgggtaccaacaaggtggctat
 181 caacagtacaatcccgacgccggttaccagcaacagtataatcctcaaggaggctatcaa
 241 cagtacaatcctcaaggcggttatcagcagcaattcaatccacaaggtggccgtggaaat
 301 tacaaaaacttcaactacaataacaatttgcaaggatatcaagctggtttccaaccacag
 361 tctcaaggtatgtctttgaacgactttcaaaagcaacaaaagcaggccgctcccaaacca
 421 aagaagactttgaagcttgtctccagttccggtatcaagttggccaatgctaccaagaag
 481 gttggcacaaaacctgccgaatctgataagaaagaggaagagaagtctgctgaaaccaaa
 541 gaaccaactaaagagccaacaaaggtcgaagaaccagttaaaaaggaggagaaaccagtc
 601 cagactgaagaaaagacggaggaaaaatcggaacttccaaaggtagaagaccttaaaatc
 661 tctgaatcaacacataataccaacaatgccaatgttaccagtgctgatgccttgatcaag
 721 gaacaggaagaagaagtggatgacgaagttgttaacgatatggactccaaagaatcctta
 781 gctccccctggtagagacgaagtccctggcagtttgcttggccaggggagggggagcgta
 841 atggacttttataaaagcctgaggggaggagctacagtcaaggtttctgcatcttcgccc
 901 tcagtggctgctgcttctcaggcagattccaagcagcagaggattctccttgatttctcg
 961 aaaggctccacaagcaatgtgcagcagcgacagcagcagcagcagcagcagcagcagcag
1021 cagcagcagcagcagcagcagcagccagacttatccaaagccgtttcactgtccatgggg
1081 ctgtatatgggagagacagaaacaaaagtgatggggaatgacttgggctacccacagcag
1141 ggccaacttggcctttcctctggggaaacagactttcggcttctggaagaaagcattgca
1201 aacctcaataggtcgaccagcgttccagagaaccccaagagttcaacgtctgcaactggg
1261 tgtgctaccccgacagagaaggagtttcccaaaactcactcggatgcatcttcagaacag
1341 aaaatcgaaaaagccagaccggcaccaacggaggcagtgtgaaattgtatcccacagacc
1401 aaagcacctttgacctcttgaaggatttggagttttccgctgggtccccaggtaaagaca
1461 caaacgagagtccctggagatcagacctgttgatagatgaaaacttgctttctcctttgg
1521 cgggagaagatgatccattccttctcgaaggggacacgaatgaggattgtaagcctctta
1581 ttttaccggacactaaacctaaaattaaggatactggagatacaatcttatcaagtccca
1641 gcagtgtggcactgccccaagtgaaaacagaaaaagatgatttcattgaactttgcaccc
1701 ccggggtaattaagcaagagaaactgggcccagtttattgtcaggcaagcttttctggga
1761 caaatataattggtaataaaatgtctgccatttctgttcatggtgtgagtacctctggag
1821 gacagatgtaccactatgacatgaatacagcatccctttctcagcagcaggatcagaagc
1881 ctgtttttaatgtcattccaccaattcctgttggttctgaaaactggaataggtgccaag
1941 gctccggagaggacagcctgacttccttgggggctctgaacttcccaggccggtcagtgt
2001 tttctaatgggtactcaagccctggaatgagaccagatgtaagctctcctccatccagct
2061 cgtcagcagccacgggaccacctcccaagctctgcctggtgtgctccgatgaagcttcag
2121 gatgtcattacggggtgctgacatgtggaagctgcaaagtattctttaaaagagcagtgg
2181 aaggacagcacaattacctttgtgctggaagaaacgattgcatcattgataaaattcgaa
2241 ggaaaaactgcccagcatgccgctatcggaaatgtcttcaggctggaatgaaccttgaag
2301 ctcgaaaaacaaagaaaaaaatcaaagggattcagcaagccactgcaggagtctca


Sup35p

[PSI+] is a non-Mendelian trait of Saccharomyces cerevisae that supress nonsense codons. This phenotype is due to a self-replication conformation (prion state) of a protein encoded by the gene Sup35. This protein, Sup35p, is the yeast eukariotyc release factor 3 (eRF3) and forms the translation termination complex with Sup45p (eRF1). The function of Sup35p is releasing the nascent polypeptide chain from the ribosome through GTP hydrolysis when Sup45p recognize a stop codon (Shorter and Lindquist, 2005).

Sup35p is 685 amino acids long and has three distinct parts (Fig.2). The NH2-terminus (N) is termed the prion-forming domain (PrD) because plays a critical role in Sup35p’s changes in proteic conformation and it is responsible for its prion behaviour. This domain is 114 amino acids long and has a high content in glutamine and asparagine. The middle region (M) provides a solubilizing and/or spacing function. Finally, the COOH-terminus (C) is responsible for the translation-termination activity.

File:Valencia prion sup35.jpg

In [PSI+] cells, most Sup35p is insoluble and nonfunctional, causing an increase in the translational read-through of stop codons. This trait is heritable because Sup35p in the amyloid state as every prion influences new Sup35p to adopt the same conformation and passes from mother cell to daughter. In [psi-] cells, the translation-termination factor Sup35p is soluble and functional.

Behaviour

Sup35p is a subunit of the translation termination complex. Its prionic nature has been proposed to have some effect on the stress response, as a possible mechanism to obtain modified genetic expression products. When the prionic conformation is activated, the termination of translation is less effective and thus new longer proteins form (True and Lindquist, 2000; Tyedmers et al., 2008). When the sequence corresponding to the NM domains of Sup35p is fused to other gene, the protein resulting of this construction acquires the prionic behaviour (Li and Lindquist, 2000).

On the other side, GR activates the transcription of genes preceded by GRE (Glucocorticoid Receptor Element) when steroid hormones are present (Heitzer et al., 2007). However, it becomes a constitutive transcription activator when it lacks its C terminal ligand-binding domain (Schena and Yamamoto, 1988). Because of the length of amino acids of the cut protein, this short version of GR is named GR526.

Li and Lindquist (2000) showed that the fused protein (NMGR526) is a functional constitutive transcription activator. In addition, when the prionic conformation is reached because of the presence of a certain stimulus, NMGR526 is no longer capable of inducing the activation of the gene preceded by GRE. Tyedmers et al. (2000) checked the conditions that trigger the prionic conformation and they found that heat shock is a significantly relevant factor. The cells in which the prionic conformation is induced, the process is promoted in an autocatalytic manner and all the protein is found in the prionic conformation. The cells resulting show the phenotype [PSI+].

It is important to note that the rate of the change of conformation is not equal to zero even at optimal growth conditions, and that not all the cells become [PSI+]. The rate of spontaneous activation of the switch is thought to be around 10-6 or 10-7 (Alberti et al., 2009). This process is promoted under heat stress (Tyedmers et al., 2008), probably because of the important role of heat shock proteins like Hsp104 in the formation and maintenance of the amyloid fiber (Halfmann et al., 2009). These approximate rates will have very important implications for the yeastworld model that we briefly describe in the following subsection, and with more detail in our wiki Modeling section.


Original source

We thank D. Susan Lindquist (Whitehead Institute for Biomedical Research / Howard Hughes Medical Institute / Department of Biology, MIT) for sending us the prionic system transformed E.coli strains.


Making our Biobricks

After a lot of attempts trying to make our BioBricks (we had some dificulties at different steps) we achieved our purpose: we built 2 BioBricks and we sent them to de Registry.

PCR

First of all, we needed enough amounts of DNA in order to insert them as our Biobrick into the pSB1C3 provided by the Registry. We had purified DNA from PM2 E.coli strains and from NMGR526 E.coli strains. Using these as our DNA template we amplified the quoted genes: PM2 and NMGR526. The chosen program was:

  • A first denaturation cycle: 94ºC 3min
  • 30 amplification cycles, made up of:
    • 94ºC 30s
    • 55ºC 1min
    • 72ºC 1min
  • Final step: 72ºC 7min

Digestion

Next step was the digestion of the amplified material with the enzimes EcoRI and PstI, keeping the reaction tubes during 4-5 hours at 37ºC with:

PM2

  • 1 μL PstI
  • 1μL EcoRI
  • 2,5 μL of insert PM2 (at 370,9 ng/ μL)
  • 4 μL H buffer
  • 31,5 μL water


NMGR526

  • 1 μL PstI
  • 1 μL EcoRI
  • 1,8 μL of insert NMGR526 (at 504,3 ng/ μL)
  • 4 μL H buffer
  • 32,2 μL water

Ligation

After purificating the DNA using a simple etanol precipitation protocol, we resuspended the DNA into 12 μL of water. Then, we put both plasmid and PM2 in one tube, and both plasmid and NMGR526 in another one, using these amounts of components:

  • 1 μL T4 ligase
  • 3 μL pSB1C3
  • 4 μL ligation buffer
  • Whole 12 μL of our DNA

We kept it O/N in the fridge at 4ºC.

Transformation

We transformed DH5α E.coli competent strain with our ligation product using a standard heat shock transformation protocol.

Miniprep

Before the tranformation ending O/N step, we noticed that we had grown colonies in cloramphenicol LB plaques, so we used them to make a plasmidic DNA extraction (Miniprep: High Pure Plasmid Isolation Kit, Roche. 11 754 785 001). In order to check the process had been successful, we made an electrophoresis gel, putting four careers:

  1. Ligation product digested with EcoRI
  2. Ligation product digested with PstI
  3. Ligation product digested with EcoRI and PstI
  4. Ligation product without any restriction enzyme

References

  • Alberti, S., Halfmann, R., King, O., Kapila, A., Lindquist, S. (2009). A systematic survey identifies prions and illuminates sequence features of prionogenic proteins. Cell. 137: 146-158.
  • Cobb, N.J., Surewicz, W. K. (2009). Prion diseases and their biochemical mechanisms. Biochemistry. 48: 2574–2585.
  • Cox,B.S. (1965). A cytoplasmic suppressor of super-suppressor in yeast. Heredity. 20: 505–521.
  • Halfmann, R., Alberti, S., Lindquist, S. (2009). Prions, protein homeostasis and phenotypic diversity. Trends in Cell Biology. 20: 125-133.
  • Heitzer, M.D., Wolf, I.M., Sanchez, E.R., Witchel, S.F., DeFranco, D.B. (2007). Glucocorticoid receptor phisiology. Rev. Endocr. Metab. Disord.. 8: 321-330.
  • Li, L., Lindquist, S. (2000). Creating a protein-based element of inheritance. Science. 287: 661-664.
  • Liu, Y., Zheng, Y. (2005). PM2, a group 3 LEA protein from soybean, and its 22-mer repeating region confer salt tolerance in Escherichia coli. Biochem. Biophys. Res. Com. 331: 325-332.
  • Liu, Y., Zheng, Y., Zhang, Y., Wang, W., Li, R. (2010). Soybean PM2 protein (LEA3) confers the tolerance of Escherichia coli and stabilization of enzyme activity under diverse stresses. Current Microbiology. 60: 373-378.
  • Prusiner, S.B. (1982). Novel proteinaceous infectious particles cause scrapie. Science. 216: 136–144.
  • Prusiner, S.B. (1998). Prions. PNAS. 95: 13363–13383.
  • Si, K., Lindquist, S. Kandel, E.R. (2003). A neuronal isoform of the Aplysia CPEB has prion-like properties. Cell. 115: 879-891.
  • Schena, M., Yamamoto, K.R. (1988). Mammalian glucocorticoid receptor derivatives enhance transcription in yeast. Science. 241: 965-967.
  • Shorter, J., Lindquist, S. (2005). Prions as adaptive conduits of memory and inheritance. Nature. 6: 435-450.
  • True, H.L., Lindquist, S. (2000). A yeast prion provides a mechanism for genetic variation and phenotypic diversity. Nature. 407: 477-483.
  • Tyedmers, J., Madariaga, M.L., Lindquist, S. (2008). Prion switching in response to environmental stress. PLoS Biology. 6: e294.
  • Wickner, R.B. (1994). [URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae. Science. 264: 566-569.
  • Wickner, R.B., Shewmaker, F., Kryndushkin, D., Edskes, H.K. (2008). Protein inheritance (prions) based on parallel in-register β-sheet amyloid structures. BioEssays. 30: 955-964.