摘要
vsx1(visual system homeobox-1),a homeobox gene originally identified from an adult goldfish retinal cDNA library,has been shown to regulate retina progenitor proliferation,differentiation and functional maintenance of bipolar cells in vertebrates.However,in all the examined vertebrate species,vsx1 transcripts can be also detected at the early developmental stage,suggesting that it may play an important role in regulating early embryogenesis as well.Here,we investigated the function of vsx1 in early embryogenesis of goldfish(Carassius auratus) with both overexpression and gene knockdown approaches.It was found that vsx1 overexpression specifically blocked dorsal midline structure for-mation and vsx1 knockdown led to disorganized dorsal midline structure.Whole-mount in situ hy-bridization revealed that the midline expression of ntl,a key regulatory gene for chordamesoderm,was repressed by vsx1 overexpression but enhanced in the vsx1 knockdown.Furthermore,VSX1 protein could bind ntl promoter directly and was sufficient to inhibit ntl promoter-driven reporter gene green fluorescence protein transcription.Together,these results suggested that vsx1 may act to repress ec-topic expression of ntl in neural progenitor cells to ensure neural tube development in a spatially coordinated pattern during early embryogenesis.
vsxl (visual system homeobox-1), a homeobox gene originally identified from an adult goldfish retinal cDNA library, has been shown to regulate retina progenitor proliferation, differentiation and functional maintenance of bipolar cells in vertebrates. However, in all the examined vertebrate species, vsxl transcripts can be also detected at the early developmental stage, suggesting that it may play an im- portant role in regulating early embryogenesis as well. Here, we investigated the function of vsxl in early embryogenesis of goldfish (Carassius auratus) with both overexpression and gene knockdown approaches. It was found that vsxl overexpression specifically blocked dorsal midline structure for- mation and vsxl knockdown led to disorganized dorsal midline structure. Whole-mount in situ hy- bridization revealed that the midline expression of ntl, a key regulatory gene for chordamesoderm, was repressed by vsxl overexpression but enhanced in the vsxl knockdown. Furthermore, VSX1 protein could bind ntl promoter directly and was sufficient to inhibit ntl promoter-driven reporter gene green fluorescence protein transcription. Together, these results suggested that vsxl may act to repress ec- topic expression of ntl in neural progenitor cells to ensure neural tube development in a spatially co- ordinated pattern during early embryogenesis.
基金
Supported by National Natural Science Foundation of China (Grant No.30430370)
National Key Basic Research and Development Program of China (Grant No.2004CB117401)
Doctoral Fund of Ministry of Education of China (Grant No.20050542002)