STOCK Synpr^tm1Sud Syngr1^tm1Sud Syngr3^tm1Sud Syp^tm1Sud/J

Stock number: 008415
Product name: SQI
Research areas: Neurobiology Research, Research Tools

Description

This compound mutant strain carries targeted knockouts of the Syngr1 (P29; synaptogyrin I) and Syp (P38; synaptophysin I) genes, and floxed conditional mutations of Synpr (SP2; synaptophysin II) and Syngr3 (SG3; synaptogyrin III). This strain may be useful in studies of synaptic plasticity and the role of synaptophysins and synaptogyrins in neurological systems.

Detailed description

This compound mutant strain carries targeted knockouts of the Syngr1 (P29; synaptogyrin I) and Syp (P38; synaptophysin I) genes, and floxed conditional mutations of Synpr (SP2; synaptophysin II) and Syngr3 (SG3; synaptogyrin III). The donating laboratory reports that seizures may occur after about 2 months of age, triggered by lifting mice up by the tail (highest incidence) or other sensory stimuli (less common). This strain may be useful in studies of synaptic plasticity and the role of synaptophysins and synaptogyrins in neurological systems.

(Updated February 5, 2015)

Development

This strain carries four targeted mutations, created independently then intercrossed.

Synpr (SP2) floxed conditional: LoxP sites flank exon 5. A neomycin cassette flanked by Frt sites was used for positive selection.

Syngr1 (P29) knockout: Exon 2 of this X-linked gene was replaced by a neomycin resistance cassette via homologous recombination in 129S6/SvEvTac-derived SM1 embryonic stem (ES) cells. Absence of expression was confirmed by the donating lab in total brain (Western Blot) and hippocampus (immunohistochemical).

Syngr3 (SG3) floxed conditional: LoxP sites flank exon 3, the coding portion of exon 4, and a C-terminus GFP (Venus) tag. A neomycin cassette flanked by Frt sites was used for positive selection.

Syp (P38) knockout: A genomic clone containing seven exons of the gene was used to construct a targeting vector that deletes exon 3 and most of the genomic sequence between exons 2 and 4. A centrally located neomycin resistance gene cassette was used for selection.

The genetic background of this compound mutant strain includes contributions from C57BL/6 and 129.

(Updated February 5, 2015)

Allele

Symbol: Synpr^tm1Sud
Name: targeted mutation 1, Thomas C Sudhof
MGI accession ID: MGI:4421428
Generation method: Targeted
Attributes: Conditional ready (e.g. floxed)
Marker symbol: Synpr
Marker name: synaptoporin
Marker synonyms: 1500003F20Rik; SPO
Chromosome: 14
Strain of origin: Not Specified
Molecular note: LoxP sites flank exon 5. A neomycin cassette flanked by Frt sites was used for positive selection.

Allele

Symbol: Syngr3^tm1Sud
Name: targeted mutation 1, Thomas C Sudhof
MGI accession ID: MGI:4421429
Generation method: Targeted
Attributes: Conditional ready (e.g. floxed)
Marker symbol: Syngr3
Marker name: synaptogyrin 3
Chromosome: 17
Strain of origin: Not Specified
Molecular note: LoxP sites flank exon 3, the coding portion of exon 4, and a C-terminus GFP (Venus) tag. A neomycin cassette flanked by Frt sites was used for positive selection.

Allele

Symbol: Syp^tm1Sud
Name: targeted mutation 1, Thomas C Sudhof
MGI accession ID: MGI:2179741
Generation method: Targeted
Attributes: Null/Knockout
Synonyms: syp I deficient
Marker symbol: Syp
Marker name: synaptophysin
Marker synonyms: A230093K24Rik; MRX96; MRXSYP; p38; Syn; Syp I; Syp1; XLID96
Chromosome: X
Strain of origin: Not Specified
Molecular note: A neomycin resistance cassette replaced exon 3 and flanking sequences. Western blot analysis on brain lysates from homozygous mice confirmed that no detectable encoded protein was present.

Allele

Symbol: Syngr1^tm1Sud
Name: targeted mutation 1, Thomas C Sudhof
MGI accession ID: MGI:2179744
Generation method: Targeted
Attributes: Null/Knockout
Marker symbol: Syngr1
Marker name: synaptogyrin 1
Marker synonyms: p29; Syngr1b
Chromosome: 15
Strain of origin: 129S6/SvEvTac
Molecular note: A neomycin resistance cassette replaced exon II and flanking sequences, which encodes two transmembrane domains of the encoded protein. Western blot analysis on total brain protein confirmed that no detectable encoded protein was present in homozygous mice.