Znfl1s作为视黄酸的直接靶基因,对斑马鱼后后脑前后轴的图案化至关重要

IF 2.6 Q2 Medicine
Jingyun Li , Yingmin Zhao , Luqingqing He , Yun Huang , Xiaojing Yang , Lingling Yu , Qingshun Zhao , Xiaohua Dong
{"title":"Znfl1s作为视黄酸的直接靶基因,对斑马鱼后后脑前后轴的图案化至关重要","authors":"Jingyun Li ,&nbsp;Yingmin Zhao ,&nbsp;Luqingqing He ,&nbsp;Yun Huang ,&nbsp;Xiaojing Yang ,&nbsp;Lingling Yu ,&nbsp;Qingshun Zhao ,&nbsp;Xiaohua Dong","doi":"10.1016/j.mod.2018.11.001","DOIUrl":null,"url":null,"abstract":"<div><p>RA (retinoic acid) signaling is essential for the patterning the hindbrain of vertebrates. Although hundreds of potential RA targets genes are identified, the ones other than <em>hox</em> genes playing roles in patterning anterior-posterior axis of hindbrain by mediating RA signaling remains largely unknown. Previously, we reported that <em>znfl1s</em> play essential roles in the formation of posterior neuroectoderm in zebrafish embryos. Here, we revealed that <em>znfl1s</em> play a critical role in patterning the posterior axis of hindbrain by maintaining the homeostasis of RA signaling in zebrafish embryos. Knocking down <em>znfl1s</em> shortened the length of the posterior hindbrain in a similar way of reducing RA signaling in zebrafish embryos and the defective posterior hindbrain was effectively rescued by elevating RA signaling. By performing mutagenesis assays and chromatin immunoprecipitation assays on the promoter of <em>znfl1s</em>, we demonstrated that <em>znfl1s</em> are direct target genes of RA to mediate RA signaling through a functional DR1 RA response element. Taken together, our results showed that Znfl1s are essential for patterning the anterior-posterior axis development of posterior hindbrain by acting as direct target genes of RA signaling.</p></div>","PeriodicalId":49844,"journal":{"name":"Mechanisms of Development","volume":"155 ","pages":"Pages 27-33"},"PeriodicalIF":2.6000,"publicationDate":"2019-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.mod.2018.11.001","citationCount":"0","resultStr":"{\"title\":\"Znfl1s are essential for patterning the anterior-posterior axis of zebrafish posterior hindbrain by acting as direct target genes of retinoic acid\",\"authors\":\"Jingyun Li ,&nbsp;Yingmin Zhao ,&nbsp;Luqingqing He ,&nbsp;Yun Huang ,&nbsp;Xiaojing Yang ,&nbsp;Lingling Yu ,&nbsp;Qingshun Zhao ,&nbsp;Xiaohua Dong\",\"doi\":\"10.1016/j.mod.2018.11.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>RA (retinoic acid) signaling is essential for the patterning the hindbrain of vertebrates. Although hundreds of potential RA targets genes are identified, the ones other than <em>hox</em> genes playing roles in patterning anterior-posterior axis of hindbrain by mediating RA signaling remains largely unknown. Previously, we reported that <em>znfl1s</em> play essential roles in the formation of posterior neuroectoderm in zebrafish embryos. Here, we revealed that <em>znfl1s</em> play a critical role in patterning the posterior axis of hindbrain by maintaining the homeostasis of RA signaling in zebrafish embryos. Knocking down <em>znfl1s</em> shortened the length of the posterior hindbrain in a similar way of reducing RA signaling in zebrafish embryos and the defective posterior hindbrain was effectively rescued by elevating RA signaling. By performing mutagenesis assays and chromatin immunoprecipitation assays on the promoter of <em>znfl1s</em>, we demonstrated that <em>znfl1s</em> are direct target genes of RA to mediate RA signaling through a functional DR1 RA response element. Taken together, our results showed that Znfl1s are essential for patterning the anterior-posterior axis development of posterior hindbrain by acting as direct target genes of RA signaling.</p></div>\",\"PeriodicalId\":49844,\"journal\":{\"name\":\"Mechanisms of Development\",\"volume\":\"155 \",\"pages\":\"Pages 27-33\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2019-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.mod.2018.11.001\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mechanisms of Development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S092547731830128X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mechanisms of Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S092547731830128X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

RA(视黄酸)信号对于脊椎动物后脑的模式是必不可少的。虽然已经确定了数百个潜在的RA靶基因,但除了hox基因外,通过介导RA信号传导在后脑前后轴的模式中发挥作用的基因仍然很大程度上未知。之前,我们报道了znfl1s在斑马鱼胚胎后神经外胚层的形成中起重要作用。在这里,我们发现znfl1s通过维持斑马鱼胚胎中RA信号的稳态,在后脑后轴的模式化中发挥关键作用。敲除znfl1s可以缩短斑马鱼后后脑的长度,其方式与减少斑马鱼胚胎中RA信号传导类似,并且通过提高RA信号传导有效地挽救了有缺陷的后后脑。通过对znfl1s启动子进行诱变实验和染色质免疫沉淀实验,我们证明znfl1s是RA的直接靶基因,通过功能性DR1 RA反应元件介导RA信号传导。综上所述,我们的研究结果表明,Znfl1s作为RA信号的直接靶基因,对后后脑的前后轴发育至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Znfl1s are essential for patterning the anterior-posterior axis of zebrafish posterior hindbrain by acting as direct target genes of retinoic acid

RA (retinoic acid) signaling is essential for the patterning the hindbrain of vertebrates. Although hundreds of potential RA targets genes are identified, the ones other than hox genes playing roles in patterning anterior-posterior axis of hindbrain by mediating RA signaling remains largely unknown. Previously, we reported that znfl1s play essential roles in the formation of posterior neuroectoderm in zebrafish embryos. Here, we revealed that znfl1s play a critical role in patterning the posterior axis of hindbrain by maintaining the homeostasis of RA signaling in zebrafish embryos. Knocking down znfl1s shortened the length of the posterior hindbrain in a similar way of reducing RA signaling in zebrafish embryos and the defective posterior hindbrain was effectively rescued by elevating RA signaling. By performing mutagenesis assays and chromatin immunoprecipitation assays on the promoter of znfl1s, we demonstrated that znfl1s are direct target genes of RA to mediate RA signaling through a functional DR1 RA response element. Taken together, our results showed that Znfl1s are essential for patterning the anterior-posterior axis development of posterior hindbrain by acting as direct target genes of RA signaling.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Mechanisms of Development
Mechanisms of Development 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
12.4 weeks
期刊介绍: Mechanisms of Development is an international journal covering the areas of cell biology and developmental biology. In addition to publishing work at the interphase of these two disciplines, we also publish work that is purely cell biology as well as classical developmental biology. Mechanisms of Development will consider papers in any area of cell biology or developmental biology, in any model system like animals and plants, using a variety of approaches, such as cellular, biomechanical, molecular, quantitative, computational and theoretical biology. Areas of particular interest include: Cell and tissue morphogenesis Cell adhesion and migration Cell shape and polarity Biomechanics Theoretical modelling of cell and developmental biology Quantitative biology Stem cell biology Cell differentiation Cell proliferation and cell death Evo-Devo Membrane traffic Metabolic regulation Organ and organoid development Regeneration Mechanisms of Development does not publish descriptive studies of gene expression patterns and molecular screens; for submission of such studies see Gene Expression Patterns.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信