Tail Biopsy Template

Purpose

The proper identification of transgenic animals in a litter is critical to the efficient pursuit of research and in reducing the number of animals involved in a research project. Most often the genotype is determined by analysis of DNA extracted from tissues of young mice. Analysis by the Polymerase Chain Reaction (PCR) requires the least amount of DNA. DNA for PCR analysis can be obtained from ear punches, hair samples, or oral swabs (see references 1-6). Depending on the requirements of the study, investigators are urged to consider these alternatives. Larger amounts of DNA are required for Southern Blot determination of the genotype. The IACUC has determined that obtaining tissue from a mouse for DNA analysis via tail biopsy is a safe, effective and humane procedure that causes minimal or transient pain and distress when performed properly. DNA prepared from tail biopsies is suitable for analysis by either Southern Blot or PCR.

Guidelines for Tail Biopsy

1. Procedures for tail biopsy for DNA analysis and/or genotyping must be described in an approved animal protocol.

2. Ideally, mice should be 10-21 days old. At this age, the tail tissue is soft (vertebra are not yet calcified) and the yield of DNA is highest. In addition, prompt analysis of tail tissue allows the desired mice to be identified prior to weaning which can facilitate more efficient use of cage space.

a. For mice 10-21 days of age: Because pain sensory development may be complete, and to further minimize any transient pain or distress, investigators are strongly encouraged to apply local anesthesia to the tail. Local anesthesia may be achieved by immersion of the tail in ice cold ethanol for 10 seconds. Alternatively, the tail can be disinfected with 70% ethanol and allowed to dry, followed by an application of ethyl chloride spray or other suitable anesthetic as recommended by the attending veterinarian.

b. For mice greater than 21 days of age: The use of a general anesthetic is required prior to collection of tissue. Avertin (tribromoethanol) can be used in mice by intraperitoneal injection of 0.3-0.6 mg/g. Other anesthetic agents for use in mice can be found on this web site at Anesthesia and Analgesia for Mice.

3. Manually restrain the mouse between thumb and forefinger. This is a convenient time to identify the animals using the appropriate method (i.e. ear punch, ear tag, transponder etc.).

4. With sterile scalpel, razor blade, or scissors cleanly excise the distal 5 mm of tail. If the proper procedures are followed, the yield of DNA from 5 mm of tail should exceed 50 micrograms, enough for multiple analyses. The yield of DNA does not proportionally increase as tail fragments larger than 5mm are used. If small amounts of DNA are required, investigators should consider taking only 2 mm of tail. If the analysis of the DNA is to be performed by PCR, great care should be taken to remove all tissue from the scissors or scalpel after each animal. Disinfect the scalpel or scissors between animals. If a scalpel is used, also disinfect the work surface on which the tail is placed between animals.

5. The investigator must monitor the animals to assure hemostasis after the animals are returned to the cage. Apply digital pressure, silver nitrate, or other means of hemostasis.

6. Repeat tail biopsies require general anesthesia and must be justified in the protocol.

Template

Tails are collected from 10-21 day old mice without general anesthesia. The mouse is gently but firmly grasped by skin behind the neck. To provide local anesthesia, the tail is dipped in ice cold ethanol for 10 seconds before performing the tail biopsy. A sterile scalpel, razor blade, or scissors is used to cleanly excise the distal 5 mm of the tail. Silver nitrate or direct pressure is used on the tip of the tail to effect hemostasis and the animal is returned to the cage once hemostasis is verified. Mice older than 21 days are anesthetized with Avertin before the tail biopsy is performed. Depth of anesthesia is evaluated by the toe pinch technique before the biopsy is collected from anesthetized animals.

References

1. Hofstetter JR, Zhang A, Mayeda AR, Guscar, T, Numberger JI and Lahiri DK. Genomic DNA from Mice: A Comparison of Recovery Methods and Tissue Sources. Biochem Mol Med 1997 Dec; 62(2):197-202.

2. Dennis, MB. IACUC Review of Genetic Engineering. Lab Animal 2000 Mar; 29(3):34-37.

3. Irwin MH, Moffatt RJ and Pinkert CA. Identification of Transgenic Mice by PCR Analysis of Saliva. Nat Biotechnol 1996 Sep;14(9): 1146-8.

4. Schmitteckert EM, Prokop CM and Hedrich HJ. DNA Detection in Hair of Transgenic Mice - A Simple Technique Minimizing the Distress on the Animals. Laboratory Animals 1999; 33/4: 385-389.

5. Couse JF, Davis VL, Tally WC and Korach KS. An Improved Method of Genomic DNA Extraction for Screening Transgenic Mice. National Institute of Environmental Health Sciences, National Institutes of Health. BioTechniques 1994; 17:1030-1032.

6. Malumbres M, Mangues R, Ferrer N, Lu S and Pellicer A. Isolation of High Molecular Weight DNA for Reliable Genotyping of Transgenic Mice. BioTechniques 1997; 22/6:1114-1119.