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Downregulation of N1 gene expression inhibits the initial heartbeating and heart development in axolotls

机译:N1基因表达的下调抑制a的初始心跳和心脏发育

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Recessive mutant gene c in the axolotl results in a failure of affected embryos to develop contracting hearts. This abnormality can be corrected by treating the mutant heart with RNA isolated from normal anterior endoderm or from endoderm conditioned medium. A cDNA library was constructed from the total conditioned medium RNA using a random priming technique in a pcDNAII vector. We have previously identified a clone (designated as N1) from the constructed axolotl cDNA library, which has a unique nucleotide sequence. We have also discovered that the N1 gene product is related to heart development in the Mexican axolotl [Cell Mol. Biol. Res. 41 (1995) 117]. In the present studies, we further investigate the role of N1 on heartbeating and heart development in axolotls. N1 mRNA expression has been determined by using semi-quantitative RT-PCR with specifically designed primers. Normal embryonic hearts (at stages 30-3 1) have been transfected with anti-sense oligonucleotides against N1 to determine if downregulation of N1 gene expression has any effect on normal heart development. Our results show that cardiac N1 mRNA expression is partially blocked in the hearts transfected with anti-sense nucleotides and the downregulation of N1 gene expression results in a decrease of heartbeating in normal embryos, although the hearts remain alive as indicated by calcium spike movement throughout the hearts. Confocal microscopy data indicate some myofibril disorganization in the hearts transfected with the anti-sense N1 oligonucleotides. Interestingly, we also find that N1 gene expression is significantly decreased in the mutant axolotl hearts. Our results suggest that N1 is a novel gene'in Mexican axolotls and it probably plays an important role in myofibrillogenesis and in the initiation of heartbeating during heart development. (C) 2003 Elsevier Ltd. All rights reserved
机译:轴突中的隐性突变基因c导致受影响的胚胎无法发育收缩的心脏。可以通过用从正常前内胚层或内胚层条件培养基分离的RNA处理突变心脏来纠正这种异常。使用随机引物技术在pcDNAII载体中从总条件培养基RNA构建cDNA文库。我们先前已经从构建的axolotl cDNA文库中鉴定出一个克隆(称为N1),该克隆具有唯一的核苷酸序列。我们还发现,N1基因产物与墨西哥a的心脏发育有关。生物学Res。 41(1995)117]。在当前的研究中,我们进一步调查N1在a中的心跳和心脏发育中的作用。 N1 mRNA表达已通过使用具有专门设计引物的半定量RT-PCR确定。正常胚胎心脏(在30-3 1阶段)已用针对N1的反义寡核苷酸转染,以确定N1基因表达的下调是否对正常心脏发育有任何影响。我们的结果表明,在反义核苷酸转染的心脏中,心脏N1 mRNA的表达被部分阻断,N1基因表达的下调会导致正常胚胎的心跳减弱,尽管心脏在整个过程中都保持了钙尖峰运动,但仍然存活心。共聚焦显微镜数据表明,在用反义N1寡核苷酸转染的心脏中,肌原纤维发生了一些混乱。有趣的是,我们还发现在突变的x心脏中N1基因表达显着降低。我们的结果表明,N1是墨西哥Mexican的一个新基因,它可能在肌原纤维形成和心脏发育过程中的心跳启动中起重要作用。 (C)2003 Elsevier Ltd.保留所有权利

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