Aquatic Biotechnology and Environmental Laboratory, Warnell School of Forestry and Natural Resources, University of Georgia, Athens, GA 30602, United States.
Mutat Res. 2010 Jun 1;688(1-2):36-40. doi: 10.1016/j.mrfmmm.2010.02.008. Epub 2010 Mar 1.
Spermatozoa comprise a large and homogeneous population of cells that may serve as an alternative to resource-intensive assays of transmissible mutations based on progeny. To evaluate mutagenic responses in spermatozoa derived from germ cells exposed to a mutagen at different stages of spermatogenesis, we compared cII mutant frequencies (MFs) in spermatozoa collected from male lambda transgenic medaka exposed to ethylnitrosourea (ENU) as either post-meiotic or pre-meiotic germ cells. cII MFs in spermatozoa exposed to ENU as spermatogonial stem cells were induced significantly, 9-fold, compared to controls, whereas, cII MFs in spermatozoa exposed as spermatozoa/late spermatids were not elevated. To directly compare responses in spermatozoa with those in progeny, we analyzed cII MFs directly in spermatozoa and in the offspring produced from identical sperm samples of ENU-exposed males. cII MFs in isolated spermatozoa exposed to ENU as post-meiotic germ cells were not significantly elevated, whereas 11-30% of the progeny derived from the identically exposed germ cells exhibited significantly elevated cII MFs, approximately 2-fold to >130-fold, compared to controls. The contradictory responses between spermatozoa and progeny analyses can be attributed to induced pre-mutational lesions that remain intact in spermatozoa but were not detected as mutations. Progeny analyses, by contrast, revealed mutant individuals with elevated cII mutant frequencies because persistent DNA damage in the spermatozoa was fixed as mutations in cells of the early stage embryo. Spermatozoa exposed to a mutagen as spermatogonial stem cells can provide an efficient means to detect the portion of transmissible mutations that were fixed as mutations in spermatozoa. The caveat is that direct analyses of mutations in spermatozoa excludes the contribution of mutations that arise from post-fertilization processes in cells of early stage embryos, and therefore may underestimate the actual frequency of mutant offspring.
精子包含大量同质细胞群,这些细胞可能成为基于后代的资源密集型可传播突变检测的替代方法。为了评估暴露于诱变剂的生殖细胞衍生的精子中的诱变反应,我们比较了暴露于乙基亚硝脲(ENU)的 lambda 转座 medaka 雄性精子中的 cII 突变频率(MF),ENU 作为减数分裂后或减数分裂前的生殖细胞。与对照相比,暴露于ENU 的精原干细胞中的 cII MF 显著诱导了 9 倍,而暴露于精子/晚期精子中的 cII MF 没有升高。为了直接比较精子中的反应与后代中的反应,我们直接分析了暴露于ENU 的精子和来自相同精子样本的雄性后代中的 cII MF。暴露于ENU 的减数分裂后生殖细胞中的分离精子中的 cII MF 没有显著升高,而 11-30%的来自相同暴露生殖细胞的后代表现出显著升高的 cII MF,与对照相比约为 2 倍至>130 倍。精子和后代分析之间的矛盾反应可以归因于诱导的前突变损伤,这些损伤在精子中保持完整,但未被检测为突变。相比之下,后代分析揭示了具有升高的 cII 突变频率的突变个体,因为精子中的持续 DNA 损伤被固定为早期胚胎细胞中的突变。暴露于ENU 的精原干细胞的精子可以提供一种有效的方法来检测固定在精子中的可传播突变的部分。警告是,直接分析精子中的突变排除了从早期胚胎细胞的受精后过程中产生的突变的贡献,因此可能低估了突变后代的实际频率。