reporter knock-in

3
REPORTER KNOCK-IN MOUSE BY KALYANI RAJALINGHAM In order to create a reporter knock-in mouse, one must first create a knock-in construct, and introduce them into ES cells via methods like electroporation. The target vector construct would include a 5’-arm, a 3’-arm, a LacZ gene, a neomycin gene, and HSV-tk (Figure 5). Homologous recombination between the target vector, and the wild-type allele (in genome) should in theory incorporate the foreign DNA segment of interest. Subsequently, the ES cells must be screened using a negative selection method – antibiotics like neomycin – and cultivate the cell culture. Genotyping via Southern Blotting can be carried out as a confirmation procedure (Iwatsuki et al. 2010). Generated Foxk2 +/LacZ ES cells are then injected into the host blastocyst which can then be implanted into a female foster mouse or surrogate mother. The foster mouse will give birth to chimeric mice. Chimeric mice are crossed with normal mice to obtain Foxk2 +/LacZ mice; heterozygotes can then be crossed to generate homozygous Foxk2 LacZ/LacZ mice. The tip of the tail is then cut off, and used for genotyping. Analysis of Reporter gene expression is carried out via X-gal staining. In most cases, three samples are strained: Foxk2 +/LacZ , Foxk2 LacZ/LacZ , and the wild-type (control). Histological slices or sections of the organism can be photographed. Fluorescent immunohistochemistry using antibodies against Foxk2, and β-galactosidase can further be used to validate the results obtained from the X-gal staining of the three strains (Foxk2 +/LacZ , Foxk2 LacZ/LacZ , and the wild-type) (Iwatsuki et al. 2010).

Upload: kalyani-rajalingham-married-to-dr-kane

Post on 10-Aug-2015

18 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: Reporter Knock-In

REPORTER KNOCK-IN MOUSE

BY KALYANI RAJALINGHAM

In order to create a reporter knock-in mouse, one must first create a knock-in construct, and

introduce them into ES cells via methods like electroporation. The target vector construct

would include a 5’-arm, a 3’-arm, a LacZ gene, a neomycin gene, and HSV-tk (Figure 5).

Homologous recombination between the target vector, and the wild-type allele (in genome)

should in theory incorporate the foreign DNA segment of interest. Subsequently, the ES cells

must be screened using a negative selection method – antibiotics like neomycin – and

cultivate the cell culture. Genotyping via Southern Blotting can be carried out as a

confirmation procedure (Iwatsuki et al. 2010).

Generated Foxk2+/LacZ

ES cells are then injected into the host blastocyst which can then be

implanted into a female foster mouse or surrogate mother. The foster mouse will give birth to

chimeric mice. Chimeric mice are crossed with normal mice to obtain Foxk2+/LacZ

mice;

heterozygotes can then be crossed to generate homozygous Foxk2LacZ/LacZ

mice. The tip of the

tail is then cut off, and used for genotyping.

Analysis of Reporter gene expression is carried out via X-gal staining. In most cases, three

samples are strained: Foxk2+/LacZ

, Foxk2LacZ/LacZ

, and the wild-type (control). Histological

slices or sections of the organism can be photographed.

Fluorescent immunohistochemistry using antibodies against Foxk2, and β-galactosidase can

further be used to validate the results obtained from the X-gal staining of the three strains

(Foxk2+/LacZ

, Foxk2LacZ/LacZ

, and the wild-type) (Iwatsuki et al. 2010).

Page 2: Reporter Knock-In

Figure 5: Target vector construct (LacZ = gene for production of β-galactosidase; Neo =

Neomycin (negative selection method); HSV-tk = lethal marker (positive selection

marker); 5’Arm = region homologous to genomic DNA at 5’ end; 3’Arm = region

homologous to genomic DNA at 3’ end)

Page 3: Reporter Knock-In

REFERENCES

Iwatsuki, Ken, Masatoshi Nomura, Atsushi Shibata, Reiko Ichikawa, Patricio L.m. Enciso,

Lixiang Wang, Ryoichi Takayanagi, Kunio Torii, and Hisayuki Uneyama. "Generation and

Characterization of T1R2-LacZ Knock-in Mouse." Biochemical and Biophysical Research

Communications 402.3 (2010): 495-99. Web.