Takeuchi T, Yamazaki Y, Katoh-Fukui Y, Tsuchiya R, Kondo S, Motoyama J, Higashinakagawa T
Mitsubishi Kasei Institute of Life Sciences, Machida, Tokyo, Japan.
Genes Dev. 1995 May 15;9(10):1211-22. doi: 10.1101/gad.9.10.1211.
A mouse mutation, termed jumonji (jmj), was generated by a gene trap strategy. Expression of the trapped gene (jmj gene), as monitored by X-gal staining, was detected predominantly at the midbrain-hindbrain boundary and in the cerebellum, depending on the stage of development. All embryos homozygous for the jmj mutation died before embryonic day 15.5. Some, but not all, of the homozygotes developed an abnormal groove in a region just anterior to the midbrain-hindbrain boundary on the neural plate at embryonic day 8-8.5 and showed a defect in neural tube closure in the midbrain region. Analyses of jmj cDNA revealed that the jmj gene is novel, conserved among vertebrates, and disrupted by vector insertion in the jmj homozygotes. The amino acid sequence deduced from the cDNA shared a portion of significant homology with human retinoblastoma-binding protein RBP-2 and with a putative protein encoded by human gene XE169 that escapes X-chromosome inactivation. These results suggest that jmj gene is essential for normal morphogenesis of the neural tube.
通过基因捕获策略产生了一种名为jumonji(jmj)的小鼠突变。通过X-gal染色监测,捕获基因(jmj基因)的表达主要在中脑-后脑边界和小脑中检测到,这取决于发育阶段。所有jmj突变纯合子胚胎在胚胎第15.5天之前死亡。一些(但不是全部)纯合子在胚胎第8 - 8.5天在神经板上中脑-后脑边界前方的区域形成了一条异常沟,并在中脑区域显示神经管闭合缺陷。对jmj cDNA的分析表明,jmj基因是新的,在脊椎动物中保守,并且在jmj纯合子中因载体插入而被破坏。从cDNA推导的氨基酸序列与人类视网膜母细胞瘤结合蛋白RBP - 2以及人类基因XE169编码的一种逃避X染色体失活的假定蛋白有一部分显著同源性。这些结果表明,jmj基因对于神经管的正常形态发生至关重要。