Ruan Xu Zhi, Yang Han Suo, Yao Shao Hua, Ma Fan Xin, Zhao Xin Yu, Yan Fei, Wang Chun Ting, Lai Song Tao, Deng Hong Xin, Wei Yu Quan
State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, P.R.China.
Mol Reprod Dev. 2007 Dec;74(12):1505-13. doi: 10.1002/mrd.20739.
We have identified a novel Xenopus gene (xVAP019) encoding a DUF1208 domain containing protein. Using whole-mount in situ hybridization and RT-PCR, we found abundant xVAP019 maternal transcripts in the animal hemisphere during the cleavage stages and blastula stages. During gastrulation xVAP019 is differentially expressed with higher levels in the animal helf and the highest in marginal zone, then further expressed widely at neuronal stages with strongest signals in the prospective CNS regions and the epidermal ectoderm. Subsequently xVAP019 was expressed predominantly in the head, the eyes, the otic vesicle, branchial arches, spinal cord, notochord, somites, and tailbud. It is absent or very weak in the endoderm. Injecting a morpholino oligo complementary to xVAP019 mRNA or injecting a caped xVAP019 mRNA caused most of embryos to die during gastrulation and neurulation. Overexpression of xVAP019 mRNA also led to eye defect, shorten interocular distance, small body size and abnormal pigment formation in parts of the survival embryos. Similar effects were induced by injecting the xVAP019 human homologous gene FAM92A1. Our results suggest that xVAP019 is essential for the normal ectoderm and axis mesoderm differentiation and embryos survival. This investigation is for the first time in vivo study examining the role of this novel gene and reveals an important role of xVAP019 in embryonic development.
我们鉴定出了一个新的非洲爪蟾基因(xVAP019),它编码一种含有DUF1208结构域的蛋白质。通过全胚胎原位杂交和逆转录聚合酶链反应,我们发现在卵裂期和囊胚期,动物半球中存在大量xVAP019母源转录本。在原肠胚形成期,xVAP019呈差异表达,在动物半球表达水平较高,在边缘区表达最高,随后在神经元阶段广泛表达,在前脑区和表皮外胚层信号最强。随后,xVAP019主要在头部、眼睛、耳泡、鳃弓、脊髓、脊索、体节和尾芽中表达。在内胚层中不存在或表达非常微弱。注射与xVAP019 mRNA互补的吗啉代寡核苷酸或注射带帽的xVAP019 mRNA会导致大多数胚胎在原肠胚形成期和神经胚形成期死亡。xVAP019 mRNA的过表达也会导致存活胚胎出现眼睛缺陷、眼间距缩短、体型变小和部分区域色素形成异常。注射xVAP019的人类同源基因FAM92A1也会诱导类似的效应。我们的结果表明,xVAP019对于正常的外胚层和轴中胚层分化以及胚胎存活至关重要。这项研究首次在体内研究了这个新基因的作用,并揭示了xVAP019在胚胎发育中的重要作用。