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转基因介导的斑马鱼骨骼表型变异。

Transgene-mediated skeletal phenotypic variation in zebrafish.

机构信息

Institute of Neuroscience, University of Oregon, Eugene, Oregon, USA.

School of Biology and Ecology, University of Maine, Orono, Maine, USA.

出版信息

J Fish Biol. 2021 Apr;98(4):956-970. doi: 10.1111/jfb.14300. Epub 2020 Mar 30.

Abstract

When considering relationships between genotype and phenotype we frequently ignore the fact that the genome of a typical animal, notably including that of a fish and a human, harbours a huge amount of foreign DNA. Such DNA, in the form of transposable elements, can affect genome function in a major way, and transgene biology needs to be included in our understanding of the genome. Here we examine an unexpected phenotypic effect of the chromosomally integrated transgene fli1a-F-hsp70l:Gal4VP16 that serves as a model for transgene function generally. We examine larval fras1 mutant zebrafish (Danio rerio). Gal4VP16 is a potent transcriptional activator that is already well known for toxicity and mediating unusual transcriptional effects. In the presence of the transgene, phenotypes in the neural crest-derived craniofacial skeleton, notably fusions and shape changes associated with loss of function fras1 mutations, are made more severe, as we quantify by scoring phenotypic penetrance, the fraction of mutants expressing the trait. A very interesting feature is that the enhancements are highly specific for fras1 mutant phenotypes, occurring in the apparent absence of more widespread changes. Except for the features due to the fras1 mutation, the transgene-bearing larvae appear generally healthy and to be developing normally. The transgene behaves as a genetic partial dominant: a single copy is sufficient for the enhancements, yet, for some traits, two copies may exert a stronger effect. We made new strains bearing independent insertions of the fli1a-F-hsp70l:Gal4VP16 transgene in new locations in the genome, and observed increased severities of the same phenotypes as observed for the original insertion. This finding suggests that sequences within the transgene, for example Gal4VP16, are responsible for the enhancements, rather than the effect on neighbouring host sequences (such as an insertional mutation). The specificity and biological action underlying the traits are subjects of considerable interest for further investigation, as we discuss. Our findings show that work with transgenes needs to be undertaken with caution and attention to detail.

摘要

当考虑基因型和表型之间的关系时,我们常常忽略一个事实,即典型动物的基因组,特别是鱼类和人类的基因组,蕴藏着大量的外源 DNA。这种以转座元件形式存在的 DNA 可以极大地影响基因组的功能,因此转基因生物学需要纳入我们对基因组的理解。在这里,我们研究了整合到染色体上的 fli1a-F-hsp70l:Gal4VP16 转基因的一个意外表型效应,该基因作为转基因功能的一般模型。我们研究了幼虫 fras1 突变斑马鱼(Danio rerio)。Gal4VP16 是一种强大的转录激活子,已经因毒性和介导异常转录效应而广为人知。在转基因的存在下,神经嵴衍生的颅面骨骼的表型,特别是与 fras1 功能缺失突变相关的融合和形状变化,变得更加严重,我们通过评分表型外显率来量化,即表达该特征的突变体的分数。一个非常有趣的特征是,增强作用高度特异于 fras1 突变表型,似乎没有更广泛的变化。除了由于 fras1 突变引起的特征外,携带转基因的幼虫通常看起来健康且正常发育。转基因表现为遗传部分显性:一个拷贝就足以增强,但对于某些特征,两个拷贝可能会产生更强的效果。我们制造了新的品系,在基因组的新位置携带独立插入的 fli1a-F-hsp70l:Gal4VP16 转基因,并观察到与原始插入相同的表型增强。这一发现表明,转基因内的序列,例如 Gal4VP16,是增强的原因,而不是对邻近宿主序列(如插入突变)的影响。我们讨论了这些表型背后的特性的特异性和生物学作用,这些都是进一步研究的重要课题。我们的研究结果表明,在进行转基因工作时需要谨慎并注意细节。

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