Characterisation of the genomic canine Fgf8 locus and screen for genetic variants in 4 dogs with different face types.

Kim E Haworth, Christopher Healy, Imelda M McGonnell, Matthew Binns, Paul T Sharpe
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引用次数: 4

Abstract

We are investigating the genetic basis of morphological differences in skull shape between domestic dogs of different breeds using a candidate gene approach to identify genes involved in the genetic regulation. One such candidate is Fgf8. Fgf8 is a signalling molecule important in the embryonic development and patterning of the craniofacial region. Mice conditional null for the expression of Fgf8 after E9.5 have a short foreface and a wide skull (Trumpp et al. 1999). Using a combination of bioinformatics and PCR cloning, we have characterised the genomic loci of the canine Fgf8 gene. Like the mouse homologue, it is composed of six exons and we also predict that like the mouse, there are eight alternative isoforms that are generated by alternative splicing events. We have identified a short 200 bp sequence upstream of the Fgf8 gene that is highly conserved between species and have predicted putative transcription factor binding sites using the Transfac database. Genetic analysis of 4 dogs with different skull types identified genetic variation. None of the variants however, were predicted to have any functional significance.

4只不同脸型犬Fgf8基因座特征及基因变异筛选
我们正在研究不同品种家养狗颅骨形状形态学差异的遗传基础,使用候选基因方法来识别参与遗传调控的基因。其中一个候选就是Fgf8。Fgf8是胚胎发育和颅面区形成过程中重要的信号分子。E9.5后Fgf8表达条件为零的小鼠具有较短的前额和较宽的头骨(Trumpp et al. 1999)。利用生物信息学和PCR克隆的结合,我们已经确定了犬Fgf8基因的基因组位点。与小鼠同源物一样,它由6个外显子组成,我们也预测,与小鼠一样,有8个可选的同种异构体是由可选的剪接事件产生的。我们已经确定了Fgf8基因上游200 bp的短序列,该序列在物种之间高度保守,并使用Transfac数据库预测了可能的转录因子结合位点。对4只不同颅骨类型的狗进行遗传分析,发现了遗传变异。然而,没有一种变异被预测有任何功能意义。
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