Difference between revisions of "Part:BBa K782007"
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==Characterization== | ==Characterization== | ||
− | We discovered that NicTAL part deposited in the Registry by the Slovenian iGEM2010 team [1] was missing subdomain in DNA-binding domain, so our team added this missing part on N terminal sequence. Apart from adding N terminal sequence,we added HIS tag on N terminal end and NLS on terminal C end of NicTAL12 (Figure 2). | + | We discovered that NicTAL part deposited in the Registry by the Slovenian iGEM2010 team [1] was missing subdomain in DNA-binding domain, so our team added this missing part on N terminal sequence. Apart from adding N terminal sequence,we added HIS tag on N terminal end and NLS on terminal C end of NicTAL12 (Figure 2). This construct was later used for designing TAL-based activator and repressor by adding VP16 [https://parts.igem.org/wiki/index.php?title=Part:BBa_K782066] and KRAB [https://parts.igem.org/wiki/index.php?title=Part:BBa_K782011] domain. |
− | + | [[Image:Svn_12_NicTAL10vs12.PNG]] | |
+ | |||
+ | '''Figure 2:'''Sequence alignment of NicTAL10 and NicTAL12, showing differences between constructs. | ||
Results obtained by testing NicTAL12 repressor and activator, proved that NicTAL12 binds to its bonding sites (link do BS) better than NicTAL10. | Results obtained by testing NicTAL12 repressor and activator, proved that NicTAL12 binds to its bonding sites (link do BS) better than NicTAL10. |
Revision as of 14:00, 25 September 2012
NicTAL12:NLS DNA binding domain
Introduction
TAL effectors (TALEs) are bacterial plant pathogen transcription factors, that bind to DNA by specifically recognizing one base pair with a single tandem repeat in their DNA-binding domain. A tandem TALE repeat contains 33 to 35 amino acids, where the 12th and 13th amino acid, called a “repeat variable diresidue” (RVD), are responsible for specific interactions with the corresponding base pair (Scholze and Boch, 2011).
Figure 1: Schematic representation of the construct
Characterization
We discovered that NicTAL part deposited in the Registry by the Slovenian iGEM2010 team [1] was missing subdomain in DNA-binding domain, so our team added this missing part on N terminal sequence. Apart from adding N terminal sequence,we added HIS tag on N terminal end and NLS on terminal C end of NicTAL12 (Figure 2). This construct was later used for designing TAL-based activator and repressor by adding VP16 [1] and KRAB [2] domain.
Figure 2:Sequence alignment of NicTAL10 and NicTAL12, showing differences between constructs.
Results obtained by testing NicTAL12 repressor and activator, proved that NicTAL12 binds to its bonding sites (link do BS) better than NicTAL10.
Figure 3: results of testing NicTAL12:VP16 activator and NicTAL12:KRAB repressor, shows, that NicTAL12 binds to DNA better than NicTAL10.
Single binding sequence for NicTAL:
References
Scholze, H., and Boch, J. (2011) TAL effectors are remote controls for gene activation. Curr. Opin. Microbiol. 14, 47-53.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2133
Illegal XhoI site found at 1224 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]