Strain Information | |
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Image | |
BRC No. | RBRC03743 |
Type | Transgene![]() |
Species | Mus musculus |
Strain name | B6D2-Tg(CAG/Su9-DsRed2,Acr3-EGFP)RBGS002Osb |
Former Common name | B6D2F1-Tg(CAG/su9-DsRed2,Acr3-EGFP), RBGS002Osb (Nov. 2011), RBGS-002 |
H-2 Haplotype | |
ES Cell line | |
Background strain | Jcl:B6D2F1 |
Appearance | |
Strain development | Developed by Masaru Okabe, Research Institute for Microbial Diseases, Osaka University. This transgenic line was generated by coinjected with Acr3-EGFP and CAG/su9-DsRed2 transgene constructs into fertilized eggs. C57BL/6 and DBA/2 mixed background. |
Strain description | Trangenic mice expressing GFP in sperm acrosome from acr3-EGFP and RFP in sperm mitochondoria from CAG/su9-DsRed2. The dual fluorescent sperm show normal fertilizing ability and can be observed through uterine and oviductal walls under excitation light. Acrosome reacted sperm and acrosome intact sperm are easily distinguishable from each other by red fluorescence. Acr3-EGFP, in which EGFP with a proacrosin signal peptide and proacrosin N-terminal peptide were connected to the acrosin promoter. CAG/su9-DsRed2, in which a RFP(DsRed2) is connected to the CAG promoter with a mitochondrial import signal sequence of Atp5g1(su9). |
Colony maintenance | Carrier x Noncarrier [or Crossing to Jcl:B6D2F1] |
References | Transgenic mouse sperm that have green acrosome and red mitochondria allow visualization of sperm and their acrosome reaction in vivo. Hasuwa H, Muro Y, Ikawa M, Kato N, Tsujimoto Y, Okabe M Exp. Anim., 59:105-107(2010). 20224175 |
Health Report | |
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Examination Date / Room / Rack | 2025/01/07Room:3-BRack:CSentinel mouse program 2024/10/07Room:3-BRack:CSentinel mouse program 2024/07/08Room:3-BRack:CSentinel mouse program 2024/04/08Room:3-BRack:CSentinel mouse program 2024/01/09Room:3-BRack:CSentinel mouse program 2023/10/10Room:3-BRack:CSentinel mouse program 2023/07/10Room:3-BRack:CSentinel mouse program 2023/04/10Room:3-BRack:CSentinel mouse program |
Gene | |||||||
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Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
DsRed2 | Red Fluorescent Protein (Discosoma sp.) | UN | DsRed2 | ||||
EGFP | Enhanced Green Fluorescent Protein (Aequorea victoria) | UN | EGFP | acrosin promoter | |||
su9 | mitochondria localization signal of mouse Atp5g1[ATP synthase Fo complex subunit 9 (su9)] | UN | su9 | CAG promoter (CMV-IE enhancer, chicken beta-actin promoter, rabbit beta-globin genomic DNA) |
Phenotype | |
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Annotation by Mammalian phenotyhpe ontology | |
Detailed phenotype data |
Ordering Information | |
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Donor DNA | CAG promoter (CMV-IE enhancer, chicken beta-actin promoter, rabbit beta-globin genomic DNA), mitochondria localization signal of mouse Atp5g1[ATP synthase Fo complex subunit 9 (su9)], Discosoma sp. DsRed2 cDNA, acrosin promoter, acrosin localization signal, jellyfish EGFP cDNA |
Research application | Fluorescent Proteins/lacZ System |
Specific Term and Conditions | The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. Exp. Anim., 59:105-107(2010). In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. RECIPIENT which wants to use the BIOLOGICAL RESOURCE for the purpose other than education or not-for-profit research is requested to enter into a Material Transfer Agreement with Osaka University (https://www.ccb.osaka-u.ac.jp/en/). The RECIPIENT must contact the DEPOSITOR in the case of application for any patents or commercial use based on the results from the use of the BIOLOGICAL RESOURCE. The RECIPIENT which wants to use the BIOLOGICAL RESOURCE even after five years must obtain a written consent from the DEPOSITOR again. |
Depositor | Masaru Okabe (Osaka University) |
Strain Status | ![]() ![]() ![]() |
Strain Availability | Cryopreserved sperm (within 1 month) Cryopreserved embryos (within 1 month) Live mouse (1 to 3 months) |
Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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Wang Z, Wei H, Wu Z, Zhang X, Sun Y, Gao L, Zhang W, Su YQ, Zhang M. The oocyte cumulus complex regulates mouse sperm migration in the oviduct. Commun Biol 5(1) 1327(2022) 36463362 |
Lück JC, Puchkov D, Ullrich F, Jentsch TJ. LRRC8/VRAC anion channels are required for late stages of spermatid development in mice. J Biol Chem 293(30) 11796-11808(2018) 29880644 |
Hino T, Muro Y, Tamura-Nakano M, Okabe M, Tateno H, Yanagimachi R. The Behavior and Acrosomal Status of Mouse Spermatozoa In Vitro, and Within the Oviduct During Fertilization after Natural Mating. Biol Reprod 95(3) 50(2016) 27417908 |
Luo SM, Ge ZJ, Wang ZW, Jiang ZZ, Wang ZB, Ouyang YC, Hou Y, Schatten H, Sun QY. Unique insights into maternal mitochondrial inheritance in mice. Proc Natl Acad Sci U S A 110(32) 13038-43(2013) 23878233 |