Unité Mixte de Recherche 1313 Génétique Animale et Biologie Intégrative, Institut National de la Recherche Agronomique, Jouy-en-Josas, France.
PLoS One. 2011;6(7):e22242. doi: 10.1371/journal.pone.0022242. Epub 2011 Jul 21.
The developmental pathways involved in horn development are complex and still poorly understood. Here we report the description of a new dominant inherited syndrome in the bovine Charolais breed that we have named type 2 scurs. Clinical examination revealed that, despite a strong phenotypic variability, all affected individuals show both horn abnormalities similar to classical scurs phenotype and skull interfrontal suture synostosis. Based on a genome-wide linkage analysis using Illumina BovineSNP50 BeadChip genotyping data from 57 half-sib and full-sib progeny, this locus was mapped to a 1.7 Mb interval on bovine chromosome 4. Within this region, the TWIST1 gene encoding a transcription factor was considered as a strong candidate gene since its haploinsufficiency is responsible for the human Saethre-Chotzen syndrome, characterized by skull coronal suture synostosis. Sequencing of the TWIST1 gene identified a c.148_157dup (p.A56RfsX87) frame-shift mutation predicted to completely inactivate this gene. Genotyping 17 scurred and 20 horned founders of our pedigree as well as 48 unrelated horned controls revealed a perfect association between this mutation and the type 2 scurs phenotype. Subsequent genotyping of 32 individuals born from heterozygous parents showed that homozygous mutated progeny are completely absent, which is consistent with the embryonic lethality reported in Drosophila and mouse suffering from TWIST1 complete insufficiency. Finally, data from previous studies on model species and a fine description of type 2 scurs symptoms allowed us to propose different mechanisms to explain the features of this syndrome. In conclusion, this first report on the identification of a potential causal mutation affecting horn development in cattle offers a unique opportunity to better understand horn ontogenesis.
角发育涉及的发育途径复杂且仍知之甚少。在这里,我们报告了在夏洛莱牛品种中发现的一种新的显性遗传综合征,我们将其命名为 2 型赘生物。临床检查表明,尽管表现型存在很强的变异性,但所有受影响的个体都表现出类似经典赘生物表型的角异常和颅骨额间骨缝融合。基于使用 Illumina BovineSNP50 BeadChip 基因分型数据对 57 对半同胞和全同胞后代进行的全基因组连锁分析,该基因座被定位到牛 4 号染色体上的 1.7 Mb 区间内。在该区域内,编码转录因子的 TWIST1 基因被认为是一个强有力的候选基因,因为其杂合不足会导致人类 Saethre-Chotzen 综合征,其特征是颅骨冠状骨缝融合。TWIST1 基因的测序发现了一个 c.148_157dup (p.A56RfsX87) 移码突变,预计会完全使该基因失活。对我们家系的 17 个赘生物和 20 个有角的创始人以及 48 个无关的有角对照进行基因分型,发现该突变与 2 型赘生物表型之间存在完美的关联。对来自杂合父母的 32 个个体进行的随后基因分型显示,完全突变的后代完全不存在,这与 Drosophila 和患有 TWIST1 完全不足的小鼠报道的胚胎致死性一致。最后,对模式物种的先前研究数据和 2 型赘生物症状的详细描述使我们能够提出不同的机制来解释该综合征的特征。总之,这是首次报道鉴定出一种潜在的因果突变,该突变会影响牛的角发育,为更好地理解角发生提供了一个独特的机会。