Booker Betty M, Friedrich Tara, Mason Mandy K, VanderMeer Julia E, Zhao Jingjing, Eckalbar Walter L, Logan Malcolm, Illing Nicola, Pollard Katherine S, Ahituv Nadav
Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America.
Institute for Human Genetics, University of California San Francisco, San Francisco, California, United States of America.
PLoS Genet. 2016 Mar 28;12(3):e1005738. doi: 10.1371/journal.pgen.1005738. eCollection 2016 Mar.
The molecular events leading to the development of the bat wing remain largely unknown, and are thought to be caused, in part, by changes in gene expression during limb development. These expression changes could be instigated by variations in gene regulatory enhancers. Here, we used a comparative genomics approach to identify regions that evolved rapidly in the bat ancestor, but are highly conserved in other vertebrates. We discovered 166 bat accelerated regions (BARs) that overlap H3K27ac and p300 ChIP-seq peaks in developing mouse limbs. Using a mouse enhancer assay, we show that five Myotis lucifugus BARs drive gene expression in the developing mouse limb, with the majority showing differential enhancer activity compared to the mouse orthologous BAR sequences. These include BAR116, which is located telomeric to the HoxD cluster and had robust forelimb expression for the M. lucifugus sequence and no activity for the mouse sequence at embryonic day 12.5. Developing limb expression analysis of Hoxd10-Hoxd13 in Miniopterus natalensis bats showed a high-forelimb weak-hindlimb expression for Hoxd10-Hoxd11, similar to the expression trend observed for M. lucifugus BAR116 in mice, suggesting that it could be involved in the regulation of the bat HoxD complex. Combined, our results highlight novel regulatory regions that could be instrumental for the morphological differences leading to the development of the bat wing.
导致蝙蝠翅膀发育的分子事件在很大程度上仍不为人知,并且被认为部分是由肢体发育过程中基因表达的变化引起的。这些表达变化可能是由基因调控增强子的变异所引发的。在这里,我们采用了一种比较基因组学方法来识别在蝙蝠祖先中快速进化但在其他脊椎动物中高度保守的区域。我们发现了166个蝙蝠加速区域(BARs),它们与发育中的小鼠肢体中的H3K27ac和p300 ChIP-seq峰重叠。使用小鼠增强子检测,我们表明五个大足鼠耳蝠BARs在发育中的小鼠肢体中驱动基因表达,与小鼠直系同源BAR序列相比,大多数显示出不同的增强子活性。其中包括BAR116,它位于HoxD簇的端粒处,在胚胎第12.5天,大足鼠耳蝠序列在前肢有强烈表达,而小鼠序列则无活性。对纳塔尔皱唇蝠Hoxd10 - Hoxd13的发育肢体表达分析显示,Hoxd10 - Hoxd11在前肢高表达而后肢低表达,这与在小鼠中观察到的大足鼠耳蝠BAR116的表达趋势相似,表明它可能参与了蝙蝠HoxD复合体的调控。综合来看,我们的结果突出了新的调控区域,这些区域可能对导致蝙蝠翅膀发育的形态差异具有重要作用。