Laboratory Animals > Volume 43, Number 1 > Pp. 1-10

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Analysis of breeding and pathology helps refine management practices of a large-scale N'-ethyl-N'-nitrosourea mouse mutagenesis programme

A P L Smith ¹, S Polley ², S Wells ², M Stewart ², L Vizor ², J Humphreys ¹, M V Warren ^3 4, N Dear ^2 5 and M T Cheeseman ¹ 

¹ Pathology Group, Mary Lyon Centre, Medical Research Council, Harwell, Oxfordshire OX11 0RD, UK; ² Mary Lyon Centre, Medical Research Council, Harwell, Oxfordshire OX11 0RD, UK; ³ The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK; ⁴ Department of Pathology, University of Cambridge, Addenbrookes Hospital, Cambridge CB2 2QQ, UK; ⁵ Current address: Mammalian Genetics of Disease Group, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield S10 2RX, UK

Corresponding author: Michael T Cheeseman. Email: m.cheeseman{at}har.mrc.ac.uk

N'-ethyl-N'-nitrosourea (ENU) is a powerful germline mutagen used in conjunction with phenotype-driven screens to generate novel mouse mutants. ENU also induces genetic lesions in somatic cells and dosage requires optimization between maximum germline mutation rate versus induced sterility and tumourigenesis that compromise the welfare and fecundity of the ENU-treated males. Here, we present our experience with BALB/cAnNCrl and C57BL/6J mice in terms of the pathology induced by ENU and its impact on breeding. In both mouse strains, morbidity and mortality rises with ENU dose. In more than 75% of C57BL/6J males, morbidity and mortality were attributable to the development of malignant T-lymphoblastic lymphoma. Approximately 50% of ENU-treated BALB/cAnNCrl males develop early malignant T-lymphoblastic lymphoma, but the cohort that survives develops late-onset lung carcinoma. Within strains, the latency of these clinically important tumour(s) was not dosage-dependent, but the proportion of mice developing tumours and consequently removed from the breeding programme increased with ENU dosage. The median number of offspring per ENU-treated C57BL/6J male in standard matings with C3H/HeH females decreased with increasing dosage. The two most important underlying causes for lower male fecundity were increased infertility in the highest dosage group and reduced numbers of litters born to the remaining fertile C57BL/6J males due to a higher incidence of morbidity. These findings have allowed us to refine breeding strategy. To maximize the number of offspring from each ENU-treated male, we now rotate productive males between two cages to expose them to more females. This optimizes the number of mutation carrying offspring while reducing the number of ENU-treated males that must be generated.

Key Words: N'-ethyl-N'-nitrosourea • mouse mutagenesis • pathology • breeding management

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