| NBRP Rat No: 0851 |
Strain name: SHR-Apoeem1Izm Prdx2em1Izm |
Commmon Name: |
Rat Genome Database |
| Principal Investigator: |
Tohru Nabika Shimane University, School of Medicine 89-1 Enya-cho, Izumo 693-8901 Shimane Japan |
| Tel: 0853-20-2136 Fax: 0853-20-2135 |
Email: nabika@med.shimane-u.ac.jp |
| Preservation Status: |
Embryo Sperm Living Animals |
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| Coat Color |
白色 |
| Inbred Generations |
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| Usage Restrictions |
The recipient of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. |
| Genetic Status |
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| Comercial Availability |
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| Research Category |
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| Gene Affected |
Apoe: Apolipoprotein E(Rattus norvegicus)、Prdx2: Peroxiredoxin-2(Rattus norvegicus) |
| Origin |
Apoe knockout SHR/Izm rats (SHR-Apoeem1Izm, NBRP-Rat No.0810) and Prdx2 knockout SHR/Izm rats (SHR-Prdx2em1Izm, NBRP-Rat No.0814) were generated by co-introducing a guide RNA targeting Apoe or Prdx2 gene and a Cas9 nuclease expression plasmid into fertilized eggs of SHR/Izm rats to induce deletion of the gene sequence at the Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University.
This strain, Apoe-Prdx2 double knockout SHR/Izm rat was generated by crossing the Apoe and Prdx2 knockout SHR/Izm rat strains by the depositor, after introduced into the Department of Experimental Animals, Shimane University.
There is a 13-base deletion in exon 2 of Apoe (5'-GCCCTGCTGTTGG-3', c.16_28del13), and a 7-base deletion in exon 2 of Prdx2 (5'-CTCCGGC-3', c.6_13del7).
Details of the target sequences are as follows: Apoe: 5'-CCTGCTGTTGGTCCCATTGCTGA-3' (5'-side CCT is the PAM sequence, the sequence below is the target sequence of the guide RNA), Prdx2: 5'-CCTCCGGCAACGCGCACATCGGA-3' (5'-side CCT is the PAM sequence, the sequence below is the target sequence of the guide RNA) |
| Strain characteristics |
The effects of increased oxidative stress on the development of atherosclerosis were examined in SHR/Izm rats lacking both the Apoe gene and Prdx2 gene. A high-fat, high-cholesterol diet (HFD) did not result in mature atheroma. Furthermore, salt loading promoted the progression of fat deposition but did not promote the development of atheroma. |
| Breeding Conditions |
Maintained by mating siblings of homozygous deletion of Apoe and Prdx2 genes. |
| Genotyping |
This can be determined by PCR using primers designed to flank the deletion region, or by sequencing of genomic DNA. The primers designed by the depositor are as follows:
For Apoe deletion confirmation (F: AGGACTGGGAGCTGGAATTT, R: AGCTGCTCAGGGCTATTGAA), for Prdx2 deletion confirmation (F: CCAAAAGTGACCTTGGGAAG, R: TCCTTAAAGGCACCATCCAC).
Product size for Apoe: Wild-type: 372 bp, Apoeem1 (Δ13): 359 bp. For Prdx2: Wild-type: 162 bp, Prdx2em1 (Δ7): 155 bp |
| References |
H Matsuo, K Kawakami, H Ohara, T Kaneko, T Mashimo, T Yamada, T Nabika
Apolipoprotein E-depletion accelerates arterial fat deposition in the spontaneously hypertensive rat
Exp Anim. 2023 Nov 9;72(4):439-445. |
| Additional strain information |
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