Part:BBa_J31001:Design

DNA invertase Hin tagged with LVA

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
  COMPATIBLE WITH RFC[1000]

Hin Invertase

Figure 1. 3-D structure of a Hin protein complex bound to DNA. View the [http://www.rcsb.org/pdb/explore/explore.do?structureId=1ZR4 interactive 3-D Jmol image].

To the left is a 3-D model of the a Hin/ DNA complex crystal structure (Figure 1, Protein Data Bank ID 1ZR4, Li et al. 2005). A Hin protein dimer binds each HixC sequence flanking the fragment of DNA to be inverted. The two dimers (dimer 1 = leftward green and blue protein structures; dimer 2 = rightward yellow and purple protein structures) come together to form a tetrad complex where cleaved DNA ends are swapped and ligated (Richards and Johnson 2004).

Design Notes

The Biobricks on this part are not wildtype but the cut sites are still viable.

Standard BioBrick Cloning Sites (Knight)

5'--GAATTC GCGGCCGC T TCTAGA G ----insert---- T ACTAGT A GCGGCCG CTGCAG-- 3'--CTTAAG CGCCGGCG A AGATCT C -------------- A TGATCA T CGCCGGC GACGTC--

BBa_J31001 Cloning Sites

5'--GAATTC GCGGCCGC * TCTAGA * --Hin coding-- * ACTAGT T GCGGCCGCCTGCAG-- 3'--CTTAAG CGCCGGCG * AGATCT * -------------- * TGATCA A CGCCGGCGGACGTC-- Prefix There is no T spacer (*) between the NotI site and the XbaI site. There is no G spacer (*) between the XbaI and the Hin coding region. Suffix There is no T spacer (*) between the Hin coding region and the SpeI site. The A spacer between the SpeI and the NotI has changed to a T. There is an extra C between the NotI site and the PstI site

Data

Inversion of HixC-flanked DNA in the presence of HinLVA HinLVA has been assembled with a pLac promoter and RBS (see BBa_S03536) to create a HinLVA expression casette. We observe inversion of HixC-flanked segments of DNA in the presence of this casette. Figure 2 shows the sizes of predicted NheI restriction fragments for different confirmations of two HixC-flanked DNA segments. The forward orientation of pBad yeilds a 200 bp fragment, while the reverse orientation yields a larger 300 bp fragment (Figure 3, lanes 2 and 3, respectively). In the presence of Hin, a plasmid originally containing pBad in the forward orientation shows restriction fragments for both orientations (Figure 3, lane 4). Similar results are seen for a HixC-flanked RBS-Tet resistance segment (Figure 4). The occurrence of the two orientations in roughly equal proportions suggests that inversion has reached a steady state. Inversion occurs without IPTG induction of pLac-Hin. This may be caused by Hin expression via read-through from the vector backbone or leaky transcription from pLac.
File:NheI map.jpg Figure 2. Predicted NheI fragments for different conformations of the different HixC-flanked DNA fragments tested.	Figure 3. An NheI digest detects Hin-mediated flipping of a HixC-flanked pBad promoter.	Figure 4. An NheI digest detects Hin-mediated flipping of a HixC-flanked coding region (RBS-Tet).

Source

Hin invertase (BBa_J31000) from Salmonella typhimurium and the LVA degredation tag (BBa_M0040).

References

• Li, W., Kamtekar, S., Xiong, Y., Sarkis, G.J., Grindley, N.D., Steitz, T.A. (2005) Structure of a synaptic gamma delta resolvase tetramer covalently linked to two cleaved DNAs. Science. 309: 1210-1215
• Sanders, E.R., Johnson, R.C. (2004) Stepwise Dissection of the Hin-catalyzed Recombination Reaction from Synapsis to Resolution. J. Mol. Biol. 340: 753–766.
• Knight, Tom. Idempotent Vector Design for Standard Assembly of Biobricks