GSK3β控制着淋巴细胞2-4个细胞阶段第五螺旋分裂的时间和模式。

IF 0.8 3区 生物学 Q4 CELL BIOLOGY
Development Genes and Evolution Pub Date : 2019-05-01 Epub Date: 2019-01-10 DOI:10.1007/s00427-018-00625-1
Hiromi Takahashi, Masanori Abe, Reiko Kuroda
{"title":"GSK3β控制着淋巴细胞2-4个细胞阶段第五螺旋分裂的时间和模式。","authors":"Hiromi Takahashi, Masanori Abe, Reiko Kuroda","doi":"10.1007/s00427-018-00625-1","DOIUrl":null,"url":null,"abstract":"<p><p>Establishment of the body plan of multicellular organisms by the primary body axis determination and cell-fate specification is a key issue in biology. We have examined the mRNA localization of three Wnt pathway components gsk3β, β-catenin, and disheveled and investigated the effects of four selective inhibitors of these proteins on the early developmental stages of the spiral cleavage embryo of the fresh water snail Lymnaea (L.) stagnalis. mRNAs for gsk3β and β-catenin were distributed uniformly throughout the embryo during development whereas disheveled mRNA showed specific localization with intra- and inter-blastomere differences in concentration along the A-V axis during spiral cleavages. Remarkably, through inhibitor studies, we identified a short sensitive period from the 2- to 4-cell stage in which GSK3β inhibition by the highly specific 1-azakenpaullone (AZ) and by LiCl induced a subsequent dramatic developmental delay and alteration of the cleavage patterns of blastomeres at the fifth cleavage (16- to 24-cell stage) resulting in exogastrulation and other abnormalities in later stages. Inhibition of β-Catenin or Disheveled had no effect. Our inhibitor experiments establish a novel role for GSK3β in the developmental timing and orientated cell division of the snail embryo. Further work will be needed to identify the downstream targets of the kinase.</p>","PeriodicalId":50588,"journal":{"name":"Development Genes and Evolution","volume":"229 2-3","pages":"73-81"},"PeriodicalIF":0.8000,"publicationDate":"2019-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"GSK3β controls the timing and pattern of the fifth spiral cleavage at the 2-4 cell stage in Lymnaea stagnalis.\",\"authors\":\"Hiromi Takahashi, Masanori Abe, Reiko Kuroda\",\"doi\":\"10.1007/s00427-018-00625-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Establishment of the body plan of multicellular organisms by the primary body axis determination and cell-fate specification is a key issue in biology. We have examined the mRNA localization of three Wnt pathway components gsk3β, β-catenin, and disheveled and investigated the effects of four selective inhibitors of these proteins on the early developmental stages of the spiral cleavage embryo of the fresh water snail Lymnaea (L.) stagnalis. mRNAs for gsk3β and β-catenin were distributed uniformly throughout the embryo during development whereas disheveled mRNA showed specific localization with intra- and inter-blastomere differences in concentration along the A-V axis during spiral cleavages. Remarkably, through inhibitor studies, we identified a short sensitive period from the 2- to 4-cell stage in which GSK3β inhibition by the highly specific 1-azakenpaullone (AZ) and by LiCl induced a subsequent dramatic developmental delay and alteration of the cleavage patterns of blastomeres at the fifth cleavage (16- to 24-cell stage) resulting in exogastrulation and other abnormalities in later stages. Inhibition of β-Catenin or Disheveled had no effect. Our inhibitor experiments establish a novel role for GSK3β in the developmental timing and orientated cell division of the snail embryo. Further work will be needed to identify the downstream targets of the kinase.</p>\",\"PeriodicalId\":50588,\"journal\":{\"name\":\"Development Genes and Evolution\",\"volume\":\"229 2-3\",\"pages\":\"73-81\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2019-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Development Genes and Evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s00427-018-00625-1\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2019/1/10 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Development Genes and Evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00427-018-00625-1","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/1/10 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

通过确定主体轴和确定细胞命运来确定多细胞生物的机体计划是生物学中的一个关键问题。我们检测了Wnt通路三种组分gsk3β、β-catenin和disheveled的mRNA定位,并研究了这些蛋白的四种选择性抑制剂对淡水蜗牛lynaea (L.)停滞螺螺旋切割胚胎早期发育阶段的影响。gsk3β和β-catenin mRNA在胚胎发育过程中均匀分布,而在螺旋切割过程中,mRNA在卵裂球内和卵裂球间沿A-V轴的浓度差异显示出特异性定位。值得注意的是,通过抑制剂研究,我们发现在2- 4细胞阶段有一个短暂的敏感期,在此期间,高度特异性的1-azakenpaullone (AZ)和LiCl对GSK3β的抑制诱导了随后的显著发育延迟和卵裂球第五次分裂(16- 24细胞阶段)切割模式的改变,导致后期的外泌乳和其他异常。抑制β-Catenin或Disheveled均无效果。我们的抑制剂实验确定了GSK3β在蜗牛胚胎发育时间和定向细胞分裂中的新作用。需要进一步的工作来确定激酶的下游靶标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GSK3β controls the timing and pattern of the fifth spiral cleavage at the 2-4 cell stage in Lymnaea stagnalis.

Establishment of the body plan of multicellular organisms by the primary body axis determination and cell-fate specification is a key issue in biology. We have examined the mRNA localization of three Wnt pathway components gsk3β, β-catenin, and disheveled and investigated the effects of four selective inhibitors of these proteins on the early developmental stages of the spiral cleavage embryo of the fresh water snail Lymnaea (L.) stagnalis. mRNAs for gsk3β and β-catenin were distributed uniformly throughout the embryo during development whereas disheveled mRNA showed specific localization with intra- and inter-blastomere differences in concentration along the A-V axis during spiral cleavages. Remarkably, through inhibitor studies, we identified a short sensitive period from the 2- to 4-cell stage in which GSK3β inhibition by the highly specific 1-azakenpaullone (AZ) and by LiCl induced a subsequent dramatic developmental delay and alteration of the cleavage patterns of blastomeres at the fifth cleavage (16- to 24-cell stage) resulting in exogastrulation and other abnormalities in later stages. Inhibition of β-Catenin or Disheveled had no effect. Our inhibitor experiments establish a novel role for GSK3β in the developmental timing and orientated cell division of the snail embryo. Further work will be needed to identify the downstream targets of the kinase.

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
Development Genes and Evolution
Development Genes and Evolution 生物-发育生物学
CiteScore
4.30
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: Development Genes and Evolution publishes high-quality reports on all aspects of development biology and evolutionary biology. The journal reports on experimental and bioinformatics work at the systemic, cellular and molecular levels in the field of animal and plant systems, covering key aspects of the following topics: Embryological and genetic analysis of model and non-model organisms Genes and pattern formation in invertebrates, vertebrates and plants Axial patterning, embryonic induction and fate maps Cellular mechanisms of morphogenesis and organogenesis Stem cells and regeneration Functional genomics of developmental processes Developmental diversity and evolution Evolution of developmentally relevant genes Phylogeny of animals and plants Microevolution Paleontology.
×
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