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本文引用的文献

1
Development and developmental disorders of the enteric nervous system.肠神经系统的发育和发育障碍。
Nat Rev Gastroenterol Hepatol. 2013 Jan;10(1):43-57. doi: 10.1038/nrgastro.2012.234. Epub 2012 Dec 11.
2
The enteric nervous system and neurogastroenterology.肠神经系统与神经胃肠病学。
Nat Rev Gastroenterol Hepatol. 2012 Mar 6;9(5):286-94. doi: 10.1038/nrgastro.2012.32.
3
BAPTI and BAPTISM birthdating of neurons in zebrafish.
Cold Spring Harb Protoc. 2012 Jan 1;2012(1):87-92. doi: 10.1101/pdb.prot067520.
4
Development of the zebrafish enteric nervous system.斑马鱼肠道神经系统的发育
Methods Cell Biol. 2011;101:143-60. doi: 10.1016/B978-0-12-387036-0.00006-2.
5
Asymmetrical distribution of non-conserved regulatory sequences at PHOX2B is reflected at the ENCODE loci and illuminates a possible genome-wide trend.PHOX2B处非保守调控序列的不对称分布在ENCODE基因座上得以体现,并揭示了一种可能的全基因组趋势。
BMC Genomics. 2009 Jan 7;10:8. doi: 10.1186/1471-2164-10-8.
6
Functional development of the enteric nervous system--from migration to motility.肠道神经系统的功能发育——从迁移到蠕动
Neurogastroenterol Motil. 2008 May;20 Suppl 1:20-31. doi: 10.1111/j.1365-2982.2008.01098.x.
7
Critical numbers of neural crest cells are required in the pathways from the neural tube to the foregut to ensure complete enteric nervous system formation.从神经管到前肠的通路中需要关键数量的神经嵴细胞,以确保完整的肠神经系统形成。
Development. 2008 May;135(9):1681-91. doi: 10.1242/dev.017418. Epub 2008 Apr 2.
8
Metrics of sequence constraint overlook regulatory sequences in an exhaustive analysis at phox2b.在对phox2b进行详尽分析时,序列约束指标忽略了调控序列。
Genome Res. 2008 Feb;18(2):252-60. doi: 10.1101/gr.6929408. Epub 2007 Dec 10.
9
The Tol2kit: a multisite gateway-based construction kit for Tol2 transposon transgenesis constructs.Tol2试剂盒:一种基于多位点Gateway技术的用于构建Tol2转座子转基因构建体的试剂盒。
Dev Dyn. 2007 Nov;236(11):3088-99. doi: 10.1002/dvdy.21343.
10
Evaluating the biological relevance of putative enhancers using Tol2 transposon-mediated transgenesis in zebrafish.利用Tol2转座子介导的转基因技术在斑马鱼中评估假定增强子的生物学相关性。
Nat Protoc. 2006;1(3):1297-305. doi: 10.1038/nprot.2006.230.

使用Tg(-8.3bphox2b:Kaede)转基因斑马鱼对肠神经系统发育进行体内可视化。

In vivo visualization of the development of the enteric nervous system using a Tg(-8.3bphox2b:Kaede) transgenic zebrafish.

作者信息

Harrison Colin, Wabbersen Tara, Shepherd Iain T

机构信息

Department of Biology, Emory University, Atlanta, Georgia.

出版信息

Genesis. 2014 Dec;52(12):985-90. doi: 10.1002/dvg.22826. Epub 2014 Nov 4.

DOI:10.1002/dvg.22826
PMID:25264359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5804488/
Abstract

The phox2b gene encodes a transcription factor that is expressed in the developing enteric nervous system (ENS). An enhancer element has been identified in the zebrafish phox2b locus that can drive tissue specific expression of reporter genes in enteric neuron precursor cells. We have generated a transgenic zebrafish line in which the Kaede fluorescent protein is under the control of this phox2b enhancer. This line has stable expression of the Kaede protein in enteric neuron precursor cells over three generations. To demonstrate the utility of this line we compared the migration and division rates of enteric neuron precursor cells in wild type and the zebrafish ENS mutant lessen.

摘要

phox2b基因编码一种在发育中的肠神经系统(ENS)中表达的转录因子。在斑马鱼phox2b基因座中已鉴定出一种增强子元件,它可以驱动报告基因在肠神经元前体细胞中进行组织特异性表达。我们构建了一种转基因斑马鱼品系,其中Kaede荧光蛋白受该phox2b增强子的控制。该品系在三代以上的肠神经元前体细胞中具有稳定的Kaede蛋白表达。为了证明该品系的实用性,我们比较了野生型和斑马鱼ENS突变体lessen中肠神经元前体细胞的迁移和分裂速率。