About   Help   FAQ
Tg(tetO-DMPK*)A2352Coop
Transgene Detail
Summary
Symbol: Tg(tetO-DMPK*)A2352Coop
Name: transgene insertion A2352, Thomas A Cooper
MGI ID: MGI:6158679
Synonyms: TREDT960I
Transgene: Tg(tetO-DMPK*)A2352Coop  Location: unknown  Genetic Position: Chr1, Syntenic
Alliance: Tg(tetO-DMPK*)A2352Coop page
Transgene
origin
Strain of Origin:  FVB/NJ
Transgene
description
Transgene Type:    Transgenic (Inducible, Inserted expressed sequence)
Inducer:    doxycycline/tetracycline
Mutation:    Insertion
 
Tg(tetO-DMPK*)A2352Coop expresses 1 gene
 
Mutation detailsThe transgene contains a human genomic segment containing exons 11-15 of the DMPK gene with 960 interrupted CTG repeats (CUG>960<) in exon 15 (at the site of the endogenous CTG repeats). These interrupted repeats are generated to contain 20 CTGs separated by five nucleotide spacers. The construct also contains 307 bp of the DMPK 3' flanking region containing the natural polyadenylation signals, and two copies of the cHS4 insulator flanking the 5' and 3' ends of the expression construct to prevent effects of the chromosomal insertion site. This mutant DMPK gene is under the direction of the tetO (tet-responsive element) promoter. The transgene integrated in chromosome 1 (9,622,984-9,660,005) is accompanied by a 37 kb genomic duplication. The integration site is located in the intronic region of 2610203C22Rik. It was also noted at that time that five nucleotide changes are in the transgene compared to the human DMPK sequence. Four of these changes (in intron 11 [CCCTTGGCAgCCCCTCTCGT], intron 14 [CACCCGCCCCgTGCCACCCG], and exon 15 [TTGCCAAACCtGCTTTTTCG and CCCAGCCGGCcCCGCCCGCT]) have no known effect on the Tg. One change, in exon 15 [CCTCGGTATcTATTGT], may affect the binding site for an antisense oligo. Similar to the human gene, it was discovered that two exons in the transgene undergo alternative splicing. (J:264569)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
References
Original:  J:264569 Morriss GR, et al., Mechanisms of skeletal muscle wasting in a mouse model for myotonic dystrophy type 1. Hum Mol Genet. 2018 Aug 15;27(16):2789-2804
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
09/03/2024
MGI 6.24
The Jackson Laboratory