Difference between revisions of "Part:BBa K404103"

 
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<partinfo>BBa_K404103 short</partinfo>
 
<partinfo>BBa_K404103 short</partinfo>
  
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{| style="color:black" cellpadding="6" cellspacing="1" border="2" align="right"
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! colspan="2" style="background:#66bbff;"|[https://parts.igem.org/Part:BBa_K404103 p5 promoter]
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|-
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! colspan="2"|[[image:Freiburg10 p5 promoter.png|200px]]
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|-
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|'''BioBrick Nr.'''
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|[https://parts.igem.org/Part:BBa_K404103 BBa_K404103]
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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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|pAAV_RC from Stratagene
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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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<p style="text-align:justify;">
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The p5 promoter, located downstream of the rep and cap ORF (Figure 5: The p5 promoter of the wtAAV-2 is located upstream of the rep and cap ORF and contains several elements, which interact with Rep and endogenous proteins.)of the wtAAV-2, regulates gene expression of the two larger non-structural proteins Rep 78 and Rep 68 that are essential in genome replication and viral genome integration into several hotspots of the human chromosome. <br />
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Several binding elements for cellular and viral proteins involved in regulation can be found in the p5 promoter(Figure 1) therefore playing an important role in gene transcription, integration and replication, dependent on the presence or absence of helper viruses such as adenovirus (Ad) or herpes simplex virus (HSV) (Murphy et al. 2007). Besides regulation of gene expression, the p5 integration efficient element (p5IEE) containing the rep binding element (RBE) and a terminal resolution site (trs) is responsible for mediating site specific integration into the human genome (Philpott et al. 2002).
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<img src="https://static.igem.org/mediawiki/parts/c/cd/Freiburg10_p5_regulation.png" style="margin: 0px 30px 0px 0px;" />
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<b> Figure 1: The p5 promoter of the wtAAV-2 is located upstream of the rep and cap ORF and contains several elements, which interact with Rep and endogenous proteins </b>.
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Containing two consensus sequences for binding immediate early E1A gene product from adenoviruses (Chang et al. 1989), p5 promoter is transactivated in the presence of helper viruses whereas suppression occurs in absence of adenoviral proteins by low levels of Rep proteins (Beaton et al. 1989). Regulating of Rep78/68 by its negative feedback loop is critical since overexpression leads to cell cycle arrest in the S-phase (Berthet et al. 2005) and suppression of cellular promoters (Jing et al. 2001).
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<!-- Add more about the biology of this part here
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===Usage and Biology===
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<h3>References</h3>
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<b>Beaton, a, P Palumbo, and K I Berns,</b> "Expression from the adeno-associated virus p5 and p19 promoters is negatively regulated in trans by the rep protein.." Journal of virology 63, no. 10 (1989): 4450-4 <br />
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<b>Berthet, Carole, Kenneth Raj, Philippe Saudan, and Peter Beard,</b> "How adeno-associated virus Rep78 protein arrests cells completely in S phase.." Proceedings of the National Academy of Sciences of the United States of America 102, no. 38 (2005): 13634-9 <br />
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<b>Chang, L S, Yang Shi, and Thomas Shenk,</b> "Adeno-associated virus P5 promoter contains an adenovirus E1A-inducible element and a binding site for the major late transcription factor.." Journal of virology 63, no. 8 (1989): 3479-88
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<b>Jing, X J, V Kalman-Maltese, X Cao, Q Yang, and J P Trempe,</b> "Inhibition of adenovirus cytotoxicity, replication, and E2a gene expression by adeno-associated virus.." Virology 291, no. 1 (2001): 140-51 <br />
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<b>Murphy, Mary, Janette Gomos-Klein, Marko Stankic, and Erik Falck-Pedersen,</b> "Adeno-associated virus type 2 p5 promoter: a rep-regulated DNA switch element functioning in transcription, replication, and site-specific integration.." Journal of virology 81, no. 8 (2007): 3721-30 <br />
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<b>Philpott, Nicola J, Janette Gomos, Kenneth I Berns, and Erik Falck-Pedersen,</b> "A p5 integration efficiency element mediates Rep-dependent integration into AAVS1 at chromosome 19.." Proceedings of the National Academy of Sciences of the United States of America 99, no. 19 (2002): 12381-5 <br 7>
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</html>
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 02:28, 25 October 2010

p5 promoter

p5 promoter
Freiburg10 p5 promoter.png
BioBrick Nr. BBa_K404103
RFC standard RFC 10
Requirement pSB1C3
Source pAAV_RC from Stratagene
Submitted by [http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]

The p5 promoter, located downstream of the rep and cap ORF (Figure 5: The p5 promoter of the wtAAV-2 is located upstream of the rep and cap ORF and contains several elements, which interact with Rep and endogenous proteins.)of the wtAAV-2, regulates gene expression of the two larger non-structural proteins Rep 78 and Rep 68 that are essential in genome replication and viral genome integration into several hotspots of the human chromosome.
Several binding elements for cellular and viral proteins involved in regulation can be found in the p5 promoter(Figure 1) therefore playing an important role in gene transcription, integration and replication, dependent on the presence or absence of helper viruses such as adenovirus (Ad) or herpes simplex virus (HSV) (Murphy et al. 2007). Besides regulation of gene expression, the p5 integration efficient element (p5IEE) containing the rep binding element (RBE) and a terminal resolution site (trs) is responsible for mediating site specific integration into the human genome (Philpott et al. 2002).

Figure 1: The p5 promoter of the wtAAV-2 is located upstream of the rep and cap ORF and contains several elements, which interact with Rep and endogenous proteins .


Containing two consensus sequences for binding immediate early E1A gene product from adenoviruses (Chang et al. 1989), p5 promoter is transactivated in the presence of helper viruses whereas suppression occurs in absence of adenoviral proteins by low levels of Rep proteins (Beaton et al. 1989). Regulating of Rep78/68 by its negative feedback loop is critical since overexpression leads to cell cycle arrest in the S-phase (Berthet et al. 2005) and suppression of cellular promoters (Jing et al. 2001).


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
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 136