Difference between revisions of "Part:BBa K404127"
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[[Image:Freiburg10_Vectorplasmid composite 9.png|thumb|center|480px]]<br>
 
[[Image:Freiburg10_Vectorplasmid composite 9.png|thumb|center|480px]]<br>
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{| style="color:black; margin: 0px 0px 500px 20px;" cellpadding="6" cellspacing="1" border="2" align="right"
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! colspan="2" style="background:#66bbff;"|[https://parts.igem.org/Part:BBa_K404127 [AAV2]-left-ITR_pCMV_betaglobin_mVenus_[AAV2]-right-ITR
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]
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|-
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! colspan="2"|[[Freiburg10_Vectorplasmid composite 9.png|200px]]
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|-
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|'''BioBrick Nr.'''
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|[https://parts.igem.org/Part:BBa_K404127 BBa_K404127]
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|-
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|'''RFC standard'''
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|[https://parts.igem.org/Help:Assembly_standard_10 RFC 10]
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|-
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|'''Requirement'''
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|pSB1C3<br>
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|-
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|'''Source'''
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|Assembled vectorplasmid of prvided BioBricks
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|-
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|'''Submitted by'''
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|[http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]
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|}
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<html>
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<p style="text-align:justify;">
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The iGEM team Freiburg provides an hGH plolyadenylation sequence within the ‘Virus Construction Kit’ due to the fact that almost every eukaryotic mRNA is processed at their 3´ and 5´end except for histone mRNAs (Millevoi et al. 2006). Pre-mRNAs contain two canonical conserved sequences. First, the polyadenylation signal “AATAAA” which is recognized by the multiprotein complex and second the GT-rich region (downstream sequence element, DSE) which is located 30 nucleotides downstream of the cleavage site. The assembled 3´end-processing machinery cleaves the mRNA transcript immediately after a CA-nucleotide therefore defining the cleavage site (Danckwardt et al. 2008). 
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<img src="https://static.igem.org/mediawiki/parts/c/cd/Freiburg10_p5_regulation.png" style="margin: 0px 20px 0px 0px; width: 600px;" />
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<b> Figure 1: Assembled vectorplasmid missing the hGH termination signal.</b>.
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<br />
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<br />
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<br />
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<h3>Characterization</h3>
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<p style="width:660px; text-align:justify;">
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Recombinant AAV genomes were engineered containing the inverted terminal repeats (ITRs), a strong eukaryotic promoter and mVenus as gene of interest with and without the hGH terminator signal. Transduction of HT1080 cells with viral particles containing the rAAV genomes and measuring mVenus expression 24-hours post infection by flow cytometry demonstrated that transgene expression of the constructs lacking the hGH termination signal is significantly reduced. Therefore, the expected result that hGH is essential for mRNA processing could be confirmed. The iGEM team Freiburg_Bioware 2010 therefore suggests using the provided hGH termination signal within the Virus Construction Kit for optimal gene expression. 
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 03:41, 25 October 2010

[AAV2]-left-ITR_pCMV_betaglobin_mVenus_[AAV2]-right-ITR

Freiburg10 Vectorplasmid composite 9.png

[AAV2-left-ITR_pCMV_betaglobin_mVenus_[AAV2]-right-ITR

]

200px
BioBrick Nr. BBa_K404127
RFC standard RFC 10
Requirement pSB1C3
Source Assembled vectorplasmid of prvided BioBricks
Submitted by [http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]

The iGEM team Freiburg provides an hGH plolyadenylation sequence within the ‘Virus Construction Kit’ due to the fact that almost every eukaryotic mRNA is processed at their 3´ and 5´end except for histone mRNAs (Millevoi et al. 2006). Pre-mRNAs contain two canonical conserved sequences. First, the polyadenylation signal “AATAAA” which is recognized by the multiprotein complex and second the GT-rich region (downstream sequence element, DSE) which is located 30 nucleotides downstream of the cleavage site. The assembled 3´end-processing machinery cleaves the mRNA transcript immediately after a CA-nucleotide therefore defining the cleavage site (Danckwardt et al. 2008).

Figure 1: Assembled vectorplasmid missing the hGH termination signal..


Characterization

Recombinant AAV genomes were engineered containing the inverted terminal repeats (ITRs), a strong eukaryotic promoter and mVenus as gene of interest with and without the hGH terminator signal. Transduction of HT1080 cells with viral particles containing the rAAV genomes and measuring mVenus expression 24-hours post infection by flow cytometry demonstrated that transgene expression of the constructs lacking the hGH termination signal is significantly reduced. Therefore, the expected result that hGH is essential for mRNA processing could be confirmed. The iGEM team Freiburg_Bioware 2010 therefore suggests using the provided hGH termination signal within the Virus Construction Kit for optimal gene expression.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1319
    Illegal AgeI site found at 2039
  • 1000
    COMPATIBLE WITH RFC[1000]