Chinese Journal of Tissue Engineering Research ›› 2021, Vol. 25 ›› Issue (11): 1682-1687.doi: 10.3969/j.issn.2095-4344.3079

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Identification and survival analysis of tTA/tetO-CCKR-2 double transgenic mice

Gao Ziqing1, Ruan Sibei2, Li Li1, Ling Feng2, Tang Xiaoqin2, Kang Qingmei2, Luo Siyi2, Luo Jing2, Tang Yaping3, 4, Tang Mingxi2    

  1. 1Southwest Medical University, Luzhou 646000, Sichuan Province, China; 2Department of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou 646000, Sichuan Province, China; 3Department of Neurobiology, Southwest Medical University, Luzhou 646000, Sichuan Province, China; 4Guangzhou Women and Children’s Medical Center, Guangzhou 510000, Guangdong Province, China
  • Received:2020-06-24 Revised:2020-07-01 Accepted:2020-07-31 Online:2021-04-18 Published:2020-12-21
  • Contact: 唐明希,博士,教授,硕士生导师,西南医科大学附属医院病理科,四川省泸州市 646000 并列通讯作者:唐亚平,博士,教授,博士生导师,西南医科大学神经生物教研室,四川省泸州市 646000; 广州市妇女儿童医疗中心 ,广东省广州市 510000
  • About author:Gao Ziqing, Master candidate, Physician, Southwest Medical University, Luzhou 646000, Sichuan Province, China
  • Supported by:
    the Science and Technology Support Plan of Sichuan Provincial Department of Science and Technology, No. 14ZC0054 (to TYP); Luzhou Science and Technology Bureau-Southwest Medical University joint Funded Project, No. 2017LZXNYD-J14 (to TMX)

Abstract: BACKGROUND: The inducible forebrain-specific cholecystokinin receptor-2 (CCKR-2) double transgenic (tTA/tetO-CCKR-2 tg, abbreviated as dtg) mice are an ideal model of anxiety-related diseases. However, there is still a lack of model identification and life related data
OBJECTIVE: To identify the genomic DNA of the offspring and the specific expression of CCKR-2 transgene in the forebrain, and to analyze the survival probability of dtg mice. 
METHODS: α-CaMKII/tTA single transgenic mice and tetO-CCKR-2 single transgenic mice were cross-fertilized to construct a dtg mouse model. The genomic DNA was extracted from the tail of the offspring, and the genotypes were detected by PCR and agarose gel electrophoresis. Wild-type (WT) mice were used as controls. In situ hybridization was used to detect the expression of CCKR-2. Survival of dtg mice and WT mice (30 females and 30 males) was observed and recorded within 2 years. The study protocol was approved by the Experimental Animal Ethics Committee of Southwest Medical University, with an approval No. 20150068.
RESULTS AND CONCLUSION: Agarose gel electrophoresis results showed the molecular weight of the PCR products of dtg mice was consistent with the expected target gene fragment. In situ hybridization results showed a strong signal of CCKR-2 was detected in the forebrain of dtg mice, but hardly present in the WT mice. The median survival time of dtg mice was 76 weeks in females and 77 weeks in males. The survival probability was decreased with age in dtg mice. The survival probability of WT mice was significantly better than that of dtg mice (P < 0.001). There was no significant sex difference between males and females of dtg mice (P=0.577). Therefore, the specific expression of CCKR-2 transgene in the forebrain can be identified using PCR amplification, genomic DNA extraction, agarose gel electrophoresis, and in situ hybridization. tTA/tetO-CCKR-2 double transgenic induction may shorten the survival time of mice, but no significant difference is observed between the females and males of dtg mice.

Key words: double transgenic mouse">, genotype identification">, in situ hybridization">, survival analysis">, anxiety disorder">, fear behavior">, post-traumatic stress disorder

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