首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Zebrafish yolk-specific not really started (nrs) gene is a vertebrate homolog of the Drosophila spinster gene and is essential for embryogenesis.
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Zebrafish yolk-specific not really started (nrs) gene is a vertebrate homolog of the Drosophila spinster gene and is essential for embryogenesis.

机译:斑马鱼卵黄特异性未真正开始的基因(nrs)是果蝇spinster基因的脊椎动物同源物,对于胚胎发生至关重要。

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By using retroviral insertional mutagenesis in zebrafish, we have identified a recessive lethal mutation in the not really started (nrs) gene. The nrs mutation disrupts a gene located in linkage group 3 that is highly homologous to the spinster gene identified in Drosophila and to spinster orthologs identified in mammals. In flies, spinster encodes a membrane protein involved in lysosomal metabolism and programmed cell death in the central nervous system and in the ovary. In nrs mutant fish embryos, we detect an opaque substance in the posterior yolk cell extension at approximately 1 day after fertilization. This material progressively accumulates and by 48 hr after fertilization fills the entire yolk. By day 3 of embryogenesis, mutant embryos are severely reduced in size compared with their wild-type siblings and they die a few hours later. By in situ hybridization, we show that the nrs mRNA is expressed in the yolk cell at the time the mutant phenotype becomes apparent. In wild-type embryos, nrs message is present maternally and zygotically throughout embryogenesis and is also detected in adult animals. In nrs homozygous mutant embryos, nrs transcripts are undetectable at the time the phenotype becomes apparent, indicating that the retroviral insertion has most likely abolished expression of the nrs gene. Finally, the nrs phenotype can be partially rescued by microinjection of nrs encoding DNA. These results suggest that the nrs mutation affects an essential gene encoding a putative membrane-bound protein expressed specifically in the yolk cell during zebrafish embryogenesis.
机译:通过在斑马鱼中使用逆转录病毒插入诱变,我们已经确定了不是真正开始的(nrs)基因的隐性致死突变。 nrs突变破坏了位于连接群3中的一个基因,该基因与果蝇中鉴定的斯皮斯特基因和哺乳动物中鉴定的斯皮斯特直系同源物高度同源。在果蝇中,斯宾斯特编码一种膜蛋白,参与中枢神经系统和卵巢中的溶酶体代谢和程序性细胞死亡。在nrs突变的鱼胚胎中,我们在受精后约1天检测到卵黄质后延伸中的不透明物质。这种物质逐渐积累,并在受精后48小时充满整个蛋黄。到胚胎发生的第3天时,与野生型同胞相比,突变型胚胎的大小已严重缩小,并且在数小时后死亡。通过原位杂交,我们表明在突变表型变得明显时,卵黄细胞中表达了nrs mRNA。在野生型胚胎中,nrs信息在整个胚胎发生过程中均以母体和合子方式存在,并且在成年动物中也可以检测到。在nrs纯合突变体胚胎中,在表型变得明显时无法检测到nrs转录本,表明逆转录病毒插入极有可能消除了nrs基因的表达。最后,可以通过显微注射编码DNA的nrs来部分拯救nrs表型。这些结果表明,nrs突变会影响编码假定的膜结合蛋白的必需基因,该蛋白在斑马鱼胚胎发生过程中特别在卵黄细胞中表达。

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