Mammalian Genetics Laboratory, National Institute of Genetics, Mishima, Shizuoka, Japan.
Animal Resource Development Unit and Genetic Engineering Team, RIKEN Center for Life Science Technologies, Kobe, Hyogo, 650-0047, Japan.
Sci Rep. 2017 Oct 11;7(1):13004. doi: 10.1038/s41598-017-12532-y.
Interaction between the epithelium and mesenchyme coordinates patterning and differentiation of oral cavity structures including teeth, palatal rugae and tongue papillae. SHH is one of the key signaling molecules for this interaction. Epithelial expression of Shh in the tooth buds and tongue papillae is regulated by at least two enhancers, MRCS1 and MFCS4. However, it is unclear how the two enhancers cooperate to regulate Shh. Here, we found that simultaneous deletion of MRCS1 and MFCS4 results in the formation of a supernumerary tooth in front of the first molar. Since deletion of either single enhancer barely affects tooth development, MRCS1 and MFCS4 evidently act in a redundant fashion. Binding motifs for WNT signaling mediators are shared by MRCS1 and MFCS4, and play a central role in regulating Shh expression, indicating that the two redundant enhancers additively exert their Shh regulation by responding to WNT signal input.
上皮组织和间充质之间的相互作用协调了口腔结构的模式形成和分化,包括牙齿、腭皱襞和舌乳头。SHH 是这种相互作用的关键信号分子之一。牙蕾和舌乳头中 Shh 的上皮表达至少受两个增强子 MRCS1 和 MFCS4 的调控。然而,目前尚不清楚这两个增强子如何合作来调节 Shh。在这里,我们发现同时缺失 MRCS1 和 MFCS4 会导致第一磨牙前形成额外的牙齿。由于缺失任一个单一的增强子几乎不会影响牙齿发育,因此 MRCS1 和 MFCS4 显然以冗余的方式起作用。WNT 信号转导介质的结合基序由 MRCS1 和 MFCS4 共享,在调节 Shh 表达中起核心作用,表明这两个冗余的增强子通过响应 WNT 信号输入,通过附加方式发挥其 Shh 调节作用。