Mbd3tm2Bh
Targeted Allele Detail
|
Symbol: |
Mbd3tm2Bh |
Name: |
methyl-CpG binding domain protein 3; targeted mutation 2, Brian Hendrich |
MGI ID: |
MGI:4887391 |
Synonyms: |
Mbd32lox, mbd3f, Mbd3Flox, mdb3Ex1-Flox |
Gene: |
Mbd3 Location: Chr10:80228373-80235365 bp, - strand Genetic Position: Chr10, 39.72 cM
|
Alliance: |
Mbd3tm2Bh page
|
|
Germline Transmission: |
Earliest citation of germline transmission:
J:167984
|
Parent Cell Line: |
E14TG2a (ES Cell)
|
Strain of Origin: |
129P2/OlaHsd
|
|
Allele Type: |
|
Targeted (Conditional ready, No functional change) |
Mutation: |
|
Insertion
|
|
|
Mutation details: This allele, in which exon 1 is flanked by loxP sites, was generated in embryonic stem (ES) cells heterozygous for Mbd3tm1Bh using a negative selection approach. First, a loxP-flanked hygromycin/thymidine kinase (hyg/tk) cassette was introduced into the wild-type allele upstream of exon 1. The ES cells were re-targeted with a vector having loxP sites flanking exon 1; two rounds of exposure to 6-thioguanine selected for cells in which the hyg/tk-tagged exon 1 had been replaced by the floxed exon. Immunoblot analysis of nuclear extracts of ES cells heterozygous for this floxed allele and the null Mbd3tm1Bh allele using antibody to MBD3 demonstrated expression of both normal protein isoforms, one of which (referred to as Mbda) contains the entire methyl-CpG-binding domain (MBD) and the other (Mbdb) lacking the N-terminal half of the MBD, encoded by exon 1. Following Cre recombinase-mediated excision of exon 1, neither isoform is detected.
(J:106974, J:167984)
|
|
|
View phenotypes and curated references for all genotypes (concatenated display).
|
|
|
Original: |
J:106974 Kaji K, et al., The NuRD component Mbd3 is required for pluripotency of embryonic stem cells. Nat Cell Biol. 2006 Mar;8(3):285-92 |
All: |
7 reference(s) |
|