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首页> 外文期刊>Environmental and molecular mutagenesis. >Transgenic lambda medaka as a new model for germ cell mutagenesis.
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Transgenic lambda medaka as a new model for germ cell mutagenesis.

机译:转基因lambda medaka作为生殖细胞诱变的新模型。

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To address the need for improved approaches to study mutations transmitted to progeny from mutagen-exposed parents, we evaluated lambda transgenic medaka, a small fish that carries the cII mutation target gene, as a new model for germ cell mutagenesis. Mutations in the cII gene in progeny derived from ethyl-nitrosourea (ENU)-exposed males were readily detected. Frequencies of mutant offspring, proportions of mosaic or whole body mutant offspring, and mutational spectra differed according to germ cell stage exposed to ENU. Postmeiotic germ cells (spermatozoa/late spermatids) generated a higher frequency of mutant offspring (11%) compared to premeiotic germ cells (3.5%). Individuals with cII mutant frequencies (MF) elevated more than threefold above the spontaneous MF (3 x 10(-5)) in the range of 10(-4) to 10(-3) were mosaic mutant offspring, whereas those with MFs approaching 1 x 10(-2) were whole body mutant offspring. Mosaic mutant offspring comprised the majority of mutant offspring derived from postmeiotic germ cells, and unexpectedly, from spermatogonial stem cells. Mutational spectra comprised of two different mutations, but at identical sites were unusual and characteristic of delayed mutations, in which fixation of a second mutation was delayed following fertilization. Delayed mutations and prevalence of mosaic mutant offspring add to growing evidence that implicates germ cells in mediating processes postfertilization that contribute to genomic instability in progeny. This model provides an efficient and sensitive approach to assess germ cell mutations, expands opportunities to increase understanding of fundamental mechanisms of mutagenesis, and provides a means for improved assessment of potential genetic health risks. Environ. Mol. Mutagen., 2008. (c) 2008 Wiley-Liss, Inc.
机译:为了满足对改进的方法进行研究的必要性,我们研究了λ诱变转基因medaka(一种携带cII突变靶基因的小型鱼类)作为生殖细胞诱变的新模型,以研究改良的方法。很容易检测到来自暴露于乙基亚硝基脲(ENU)的雄性后代中cII基因的突变。突变后代的频率,镶嵌或全身突变后代的比例以及突变谱根据暴露于ENU的生殖细胞阶段而有所不同。与减数分裂前的生殖细胞(3.5%)相比,减数分裂后的生殖细胞(精子/晚期精子)产生更高频率的突变后代(11%)。具有cII突变频率(MF)的个体在10(-4)到10(-3)范围内比自发MF(3 x 10(-5))高出三倍以上,是镶嵌突变体后代,而具有MF的个体接近1 x 10(-2)是全身突变体的后代。镶嵌突变体后代包括大多数来自减数分裂后生殖细胞的突变体后代,以及出乎意料地来自精原干细胞的突变体后代。突变谱由两个不同的突变组成,但在相同的位点是不寻常的且具有延迟突变的特征,其中第二个突变的固定在受精后被延迟。延迟突变和镶嵌突变体后代的流行增加了越来越多的证据,表明生殖细胞参与了受精后的介导过程,从而导致后代的基因组不稳定。该模型提供了一种有效且敏感的方法来评估生殖细胞突变,扩大了机会,以加深对诱变的基本机制的了解,并提供了一种改进对潜在遗传健康风险评估的方法。环境。大声笑Mutagen。,2008.(c)2008 Wiley-Liss,Inc.

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