Division of Cardiology, Department of Pediatrics, Children's Hospital of Philadelphia, PA, USA.
Dev Biol. 2010 Mar 15;339(2):519-27. doi: 10.1016/j.ydbio.2009.12.030. Epub 2010 Jan 4.
Pax3 is a transcription factor expressed in somitic mesoderm, dorsal neural tube and pre-migratory neural crest during embryonic development. We have previously identified cis-acting enhancer elements within the proximal upstream genomic region of Pax3 that are sufficient to direct functional expression of Pax3 in neural crest. These elements direct expression of a reporter gene to pre-migratory neural crest in transgenic mice, and transgenic expression of a Pax3 cDNA using these elements is sufficient to rescue neural crest development in mice otherwise lacking endogenous Pax3. We show here that deletion of these enhancer sequences by homologous recombination is insufficient to abrogate neural crest expression of Pax3 and results in viable mice. We identify a distinct enhancer in the fourth intron that is also capable of mediating neural crest expression in transgenic mice and zebrafish. Our analysis suggests the existence of functionally redundant neural crest enhancer modules for Pax3.
Pax3 是一种转录因子,在胚胎发育过程中表达于体节中胚层、背侧神经管和迁移前神经嵴。我们之前已经鉴定了 Pax3 近端上游基因组区域内的顺式作用增强子元件,这些元件足以指导 Pax3 在神经嵴中的功能性表达。这些元件在转基因小鼠中指导报告基因表达到迁移前的神经嵴,并且使用这些元件的 Pax3 cDNA 的转基因表达足以挽救 otherwise lacking endogenous Pax3 的小鼠的神经嵴发育。我们在这里表明,通过同源重组缺失这些增强子序列不足以消除 Pax3 的神经嵴表达,并导致存活的小鼠。我们鉴定了第四内含子中的一个独特增强子,它也能够在转基因小鼠和斑马鱼中介导神经嵴表达。我们的分析表明 Pax3 存在功能冗余的神经嵴增强子模块。