1 / 9

Zebrafish msxe E xpression Analysis

Zebrafish msxe E xpression Analysis. Cassie Wells. Outline. m sxe /MSX1 implication in orofacial clefting Bioinformatic Analysis My project goal Tol2Kit / Gateway Cloning System Expression Clone Design Acknowledgements. Cleft Lip and/or Palate.

melody
Télécharger la présentation

Zebrafish msxe E xpression Analysis

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Zebrafish msxe Expression Analysis Cassie Wells

  2. Outline • msxe/MSX1 implication in orofacial clefting • Bioinformatic Analysis • My project goal • Tol2Kit / Gateway Cloning System • Expression Clone Design • Acknowledgements

  3. Cleft Lip and/or Palate • The most common congenital facial abnormality • Association studies have linked the gene MSX1 to clefting in humans • Murine Msx1 expression is controlled at the tips of the growing facial prominences by the two highly conserved distal and proximal enhancers, (DE and PE, respectively) Murine Msx1 expression is controlled at the tips of the growing facial prominences by the two highly conserved distal and proximal enhancers, (DE and PE, respectively) (MacKenzie et al., 1997)

  4. Bioinformatic Analysis Schematic diagram of the msxe locus • Bioinformatic analysis revealed two highly conserved enhancer regions (DE and PE), presumably corresponding to the murine enhancers identified by Mackenzie, and a putative promoter

  5. Conservation of the DE and Protein Binding Sites

  6. Project Purpose • My project purpose: To develop the first step, transgenic expression component, of an in vivo functional assay for DNA and protein coding variants at the MSX1 locus.

  7. 3 Fragment Recombination • Three PCR Products flanked by specific att sites and three Donor vectors are used in separate BP recombination reactions to generate three entry clones • The three entry clones and a destination vector are used together in a LR recombination reaction to create one expression clone

  8. pME B1. EGFP B2. msxe B3. msxe/MSX1 knock-out and rescue B4. MSX1 B5. mutant MSX1 Expression Clone Construct Possibilities p5E A1. Promoter A2. DE-Promoter A3. PE-Promoter A4. 2.1kb chunk (DE – Prom) p3E C1. pA C2. EGFPpA B pDestTol2pA2 A C

  9. Acknowledgements • Dr. Peter Jezewski (PI) • Divakar Prakash • Henry Jackson • Dr. Heidi Erlandsen • Institute of Oral Health Research

More Related