• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

斑马鱼中磷脂酶Cε1的分子克隆与表达

Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish.

作者信息

Zhou Weibin, Hildebrandt Friedhelm

机构信息

Departments of Pediatrics and Human Genetics, University of Michigan, 8220 MSRB3, 1150 W Medical Center Drive, Ann Arbor, MI 48109-5646, USA.

出版信息

Gene Expr Patterns. 2009 Jun;9(5):282-8. doi: 10.1016/j.gep.2009.03.003. Epub 2009 Mar 28.

DOI:10.1016/j.gep.2009.03.003
PMID:19332147
Abstract

Phospholipase C (PLC) is a key enzyme that generates inositol 1,4,5-triphosphate (IP(3)) and diacylglycerol (DAG), two second messengers in signal transduction. Phospholipase Cepsilon (PLCE1) is a unique member of the PLC family in that it carries both RasGEF and Ras-associating (RA) domains and may serve as an activator and an effector of small GTPases. Recently, mutations in PLCE1 have been associated with early-onset nephrotic syndrome. We have identified the zebrafish ortholog of PLCE1 and characterized its expression pattern in zebrafish embryos by in situ hybridization. Zebrafish plce1 gene encodes a protein of 2248 amino acids that shares 56% identity with mammalian PLCepsilon. During zebrafish embryonic development, plce1 is expressed in a dynamic pattern in a variety of organs, such as brain, muscle, liver, and pronephric glomeruli. Our results suggest that zebrafish may be used as a model organism to address the function of PLCepsilon during the development of these organs.

摘要

磷脂酶C(PLC)是一种关键酶,可生成肌醇1,4,5-三磷酸(IP(3))和二酰基甘油(DAG),这两种是信号转导中的第二信使。磷脂酶Cε(PLCE1)是PLC家族中的独特成员,因为它同时具有RasGEF和Ras结合(RA)结构域,并且可能作为小GTP酶的激活剂和效应器。最近,PLCE1中的突变与早发性肾病综合征有关。我们已经鉴定出斑马鱼中PLCE1的直系同源物,并通过原位杂交表征了其在斑马鱼胚胎中的表达模式。斑马鱼plce1基因编码一个2248个氨基酸的蛋白质,与哺乳动物的PLCε有56%的同源性。在斑马鱼胚胎发育过程中,plce1在多种器官中以动态模式表达,如脑、肌肉、肝脏和前肾肾小球。我们的结果表明,斑马鱼可作为一种模式生物来研究PLCε在这些器官发育过程中的功能。

相似文献

1
Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish.斑马鱼中磷脂酶Cε1的分子克隆与表达
Gene Expr Patterns. 2009 Jun;9(5):282-8. doi: 10.1016/j.gep.2009.03.003. Epub 2009 Mar 28.
2
Cloning, expression pattern and essentiality of the high-affinity copper transporter 1 (ctr1) gene in zebrafish.斑马鱼中高亲和力铜转运蛋白1(ctr1)基因的克隆、表达模式及必要性
Gene. 2004 Mar 17;328:113-20. doi: 10.1016/j.gene.2003.11.019.
3
Identification and expression pattern of zebrafish prox2 during embryonic development.斑马鱼prox2在胚胎发育过程中的鉴定及表达模式
Dev Dyn. 2008 Dec;237(12):3916-20. doi: 10.1002/dvdy.21798.
4
The molecular structures and expression patterns of zebrafish troponin I genes.斑马鱼肌钙蛋白I基因的分子结构与表达模式
Gene Expr Patterns. 2009 Jun;9(5):348-56. doi: 10.1016/j.gep.2009.02.001.
5
Differential expression of zebrafish gpia and gpib during development.斑马鱼gpia和gpib在发育过程中的差异表达。
Gene Expr Patterns. 2009 Apr;9(4):238-45. doi: 10.1016/j.gep.2008.12.006. Epub 2008 Dec 31.
6
Cloning and embryonic expression of zebrafish PLAG genes.斑马鱼PLAG基因的克隆与胚胎表达
Gene Expr Patterns. 2006 Mar;6(3):267-76. doi: 10.1016/j.modgep.2005.08.001. Epub 2005 Dec 27.
7
Molecular cloning and gene expression of the prox1a and prox1b genes in the medaka, Oryzias latipes.青鳉(Oryzias latipes)中prox1a和prox1b基因的分子克隆与基因表达
Gene Expr Patterns. 2009 Jun;9(5):341-7. doi: 10.1016/j.gep.2009.02.004. Epub 2009 Feb 20.
8
Identification and characterization of zebrafish semaphorin 6D.斑马鱼信号素6D的鉴定与特征分析。
Biochem Biophys Res Commun. 2007 Nov 23;363(3):762-8. doi: 10.1016/j.bbrc.2007.09.038. Epub 2007 Sep 20.
9
Role of a novel zebrafish nup98 during embryonic development.新型斑马鱼核孔蛋白 98 在胚胎发育中的作用。
Exp Hematol. 2010 Nov;38(11):1014-1021.e1-2. doi: 10.1016/j.exphem.2010.07.010. Epub 2010 Aug 7.
10
Zebrafish spata2 is expressed at early developmental stages.斑马鱼spata2在发育早期阶段表达。
Int J Dev Biol. 2007;51(3):241-6. doi: 10.1387/ijdb.062220em.

引用本文的文献

1
Genome-wide detection of positive and balancing signatures of selection shared by four domesticated rainbow trout populations (Oncorhynchus mykiss).基因组范围内检测四个家养虹鳟群体(Oncorhynchus mykiss)共享的正选择和平衡选择特征。
Genet Sel Evol. 2024 Feb 22;56(1):13. doi: 10.1186/s12711-024-00884-9.
2
Genetic variants related to successful migraine prophylaxis with verapamil.与维拉帕米预防偏头痛成功相关的遗传变异。
Mol Genet Genomic Med. 2021 Jun;9(6):e1680. doi: 10.1002/mgg3.1680. Epub 2021 Apr 7.
3
Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockout.
皮质类固醇治疗可加重 MAGI2A 敲除斑马鱼模型的肾病综合征。
Kidney Int. 2019 May;95(5):1079-1090. doi: 10.1016/j.kint.2018.12.026. Epub 2019 Mar 5.
4
PLCε1 regulates SDF-1α-induced lymphocyte adhesion and migration to sites of inflammation.磷脂酶Cε1(PLCε1)调节基质细胞衍生因子-1α(SDF-1α)诱导的淋巴细胞黏附以及向炎症部位的迁移。
Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):2693-2698. doi: 10.1073/pnas.1612900114. Epub 2017 Feb 17.
5
GADD45B mediates podocyte injury in zebrafish by activating the ROS-GADD45B-p38 pathway.GADD45B 通过激活 ROS-GADD45B-p38 通路介导足细胞损伤。
Cell Death Dis. 2016 Jan 21;7(1):e2068. doi: 10.1038/cddis.2015.300.
6
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling.DCDC2 突变通过破坏 Wnt 信号传导导致肾脏-肝脏纤毛病变。
Am J Hum Genet. 2015 Jan 8;96(1):81-92. doi: 10.1016/j.ajhg.2014.12.002. Epub 2014 Dec 31.
7
Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.Mg2+ 转运蛋白 SLC41A1 的突变导致类似肾单位肾痨的表型。
J Am Soc Nephrol. 2013 May;24(6):967-77. doi: 10.1681/ASN.2012101034. Epub 2013 May 9.
8
The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development.色素性视网膜炎蛋白 2 与多囊蛋白 2 相互作用并调节纤毛介导的脊椎动物发育。
Hum Mol Genet. 2010 Nov 15;19(22):4330-44. doi: 10.1093/hmg/ddq355. Epub 2010 Aug 20.
9
The expression patterns of minor fibrillar collagens during development in zebrafish.斑马鱼发育过程中小纤维胶原的表达模式。
Gene Expr Patterns. 2010 Oct-Dec;10(7-8):315-22. doi: 10.1016/j.gep.2010.07.002. Epub 2010 Jul 18.
10
Glomerular diseases: genetic causes and future therapeutics.肾小球疾病:遗传病因与未来治疗学。
Nat Rev Nephrol. 2010 Sep;6(9):539-54. doi: 10.1038/nrneph.2010.103. Epub 2010 Jul 20.