Loebel David A F, Hor Angelyn C C, Bildsoe Heidi K, Tam Patrick P L
Embryology Unit, Children's Medical Research Institute, Westmead, New South Wales, Australia; Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
Embryology Unit, Children's Medical Research Institute, Westmead, New South Wales, Australia.
PLoS One. 2014 Jun 3;9(6):e98945. doi: 10.1371/journal.pone.0098945. eCollection 2014.
Twist1 encodes a transcription factor that plays a vital role in limb development. We have used a tamoxifen-inducible Cre transgene, Ubc-CreERT2, to generate time-specific deletions of Twist1 by inducing Cre activity in mouse embryos at different ages from embryonic (E) day 9.5 onwards. A novel forelimb phenotype of supernumerary pre-axial digits and enlargement or partial duplication of the distal radius was observed when Cre activity was induced at E9.5. Gene expression analysis revealed significant upregulation of Hoxd10, Hoxd11 and Grem1 in the anterior half of the forelimb bud at E11.5. There is also localized upregulation of Ptch1, Hand2 and Hoxd13 at the site of ectopic digit formation, indicating a posterior molecular identity for the supernumerary digits. The specific skeletal phenotypes, which include duplication of digits and distal zeugopods but no overt posteriorization, differ from those of other Twist1 conditional knockout mutants. This outcome may be attributed to the deferment of Twist1 ablation to a later time frame of limb morphogenesis, which leads to the ectopic activation of posterior genes in the anterior tissues after the establishment of anterior-posterior anatomical identities in the forelimb bud.
Twist1编码一种转录因子,其在肢体发育中起着至关重要的作用。我们使用了一种他莫昔芬诱导型Cre转基因Ubc-CreERT2,通过在胚胎(E)第9.5天及以后的不同年龄诱导小鼠胚胎中的Cre活性,来产生Twist1的时间特异性缺失。当在E9.5诱导Cre活性时,观察到了一种新的前肢表型,即额外的轴前指以及桡骨远端的增大或部分重复。基因表达分析显示,在E11.5时,前肢芽前半部分的Hoxd10、Hoxd11和Grem1显著上调。在异位指形成部位,Ptch1、Hand2和Hoxd13也有局部上调,表明额外指具有后部分子特征。包括指和远端肢体中段重复但无明显后部化的特定骨骼表型,与其他Twist1条件性敲除突变体不同。这一结果可能归因于Twist1缺失推迟到肢体形态发生的较晚时间框架,这导致在前肢芽建立前后解剖特征后,前侧组织中后部基因的异位激活。