Suppr超能文献

一种在盘基网柄菌趋化性和环磷酸腺苷信号转导中所需的新型Ras相互作用蛋白。

A novel Ras-interacting protein required for chemotaxis and cyclic adenosine monophosphate signal relay in Dictyostelium.

作者信息

Lee S, Parent C A, Insall R, Firtel R A

机构信息

Department of Biology, Center for Molecular Genetics, University of California, San Diego, La Jolla, California 92093-0634, USA.

出版信息

Mol Biol Cell. 1999 Sep;10(9):2829-45. doi: 10.1091/mbc.10.9.2829.

Abstract

We have identified a novel Ras-interacting protein from Dictyostelium, RIP3, whose function is required for both chemotaxis and the synthesis and relay of the cyclic AMP (cAMP) chemoattractant signal. rip3 null cells are unable to aggregate and lack receptor activation of adenylyl cyclase but are able, in response to cAMP, to induce aggregation-stage, postaggregative, and cell-type-specific gene expression in suspension culture. In addition, rip3 null cells are unable to properly polarize in a cAMP gradient and chemotaxis is highly impaired. We demonstrate that cAMP stimulation of guanylyl cyclase, which is required for chemotaxis, is reduced approximately 60% in rip3 null cells. This reduced activation of guanylyl cyclase may account, in part, for the defect in chemotaxis. When cells are pulsed with cAMP for 5 h to mimic the endogenous cAMP oscillations that occur in wild-type strains, the cells will form aggregates, most of which, however, arrest at the mound stage. Unlike the response seen in wild-type strains, the rip3 null cell aggregates that form under these experimental conditions are very small, which is probably due to the rip3 null cell chemotaxis defect. Many of the phenotypes of the rip3 null cell, including the inability to activate adenylyl cyclase in response to cAMP and defects in chemotaxis, are very similar to those of strains carrying a disruption of the gene encoding the putative Ras exchange factor AleA. We demonstrate that aleA null cells also exhibit a defect in cAMP-mediated activation of guanylyl cyclase similar to that of rip3 null cells. A double-knockout mutant (rip3/aleA null cells) exhibits a further reduction in receptor activation of guanylyl cyclase, and these cells display almost no cell polarization or movement in cAMP gradients. As RIP3 preferentially interacts with an activated form of the Dictyostelium Ras protein RasG, which itself is important for cell movement, we propose that RIP3 and AleA are components of a Ras-regulated pathway involved in integrating chemotaxis and signal relay pathways that are essential for aggregation.

摘要

我们从盘基网柄菌中鉴定出一种新型的Ras相互作用蛋白RIP3,趋化作用以及环磷酸腺苷(cAMP)趋化信号的合成与传递都需要其发挥功能。rip3基因缺失的细胞无法聚集,腺苷酸环化酶缺乏受体激活,但在悬浮培养中,它们能够响应cAMP诱导聚集期、聚集后以及细胞类型特异性基因表达。此外,rip3基因缺失的细胞无法在cAMP梯度中正确极化,趋化作用严重受损。我们证明,趋化作用所需的cAMP对鸟苷酸环化酶的刺激在rip3基因缺失的细胞中降低了约60%。鸟苷酸环化酶激活的降低可能部分解释了趋化作用的缺陷。当用cAMP脉冲处理细胞5小时以模拟野生型菌株中发生的内源性cAMP振荡时,细胞会形成聚集体,然而,其中大多数会在丘状阶段停滞。与野生型菌株中的反应不同,在这些实验条件下形成的rip3基因缺失细胞聚集体非常小,这可能是由于rip3基因缺失细胞的趋化缺陷。rip3基因缺失细胞的许多表型,包括无法响应cAMP激活腺苷酸环化酶以及趋化缺陷,与携带假定的Ras交换因子AleA编码基因破坏的菌株非常相似。我们证明,aleA基因缺失的细胞在cAMP介导的鸟苷酸环化酶激活方面也表现出与rip3基因缺失细胞类似的缺陷。双敲除突变体(rip3/aleA基因缺失细胞)在鸟苷酸环化酶的受体激活方面进一步降低,并且这些细胞在cAMP梯度中几乎没有细胞极化或移动。由于RIP3优先与盘基网柄菌Ras蛋白RasG的激活形式相互作用,而RasG本身对细胞运动很重要,我们提出RIP3和AleA是Ras调节途径的组成部分,该途径参与整合对聚集至关重要的趋化作用和信号传递途径。

相似文献

3
A novel Dictyostelium RasGEF required for chemotaxis and development.
BMC Cell Biol. 2005 Dec 7;6:43. doi: 10.1186/1471-2121-6-43.
6
TOR complex 2 integrates cell movement during chemotaxis and signal relay in Dictyostelium.
Mol Biol Cell. 2005 Oct;16(10):4572-83. doi: 10.1091/mbc.e05-04-0342. Epub 2005 Aug 3.
8
A new HECT ubiquitin ligase regulating chemotaxis and development in Dictyostelium discoideum.
J Cell Sci. 2017 Feb 1;130(3):551-562. doi: 10.1242/jcs.194225. Epub 2017 Jan 3.
9
Multiple cyclic AMP receptors are linked to adenylyl cyclase in Dictyostelium.
Mol Biol Cell. 1992 Nov;3(11):1229-34. doi: 10.1091/mbc.3.11.1229.

引用本文的文献

1
The mTORC2 signaling network: targets and cross-talks.
Biochem J. 2024 Jan 25;481(2):45-91. doi: 10.1042/BCJ20220325.
2
TOR complex 2 is a master regulator of plasma membrane homeostasis.
Biochem J. 2022 Sep 30;479(18):1917-1940. doi: 10.1042/BCJ20220388.
3
Structural insights into Ras regulation by SIN1.
Proc Natl Acad Sci U S A. 2022 May 10;119(19):e2119990119. doi: 10.1073/pnas.2119990119. Epub 2022 May 6.
4
RAS interaction with Sin1 is dispensable for mTORC2 assembly and activity.
Proc Natl Acad Sci U S A. 2021 Aug 17;118(33). doi: 10.1073/pnas.2103261118.
5
Ras, PI3K and mTORC2 - three's a crowd?
J Cell Sci. 2020 Oct 8;133(19):jcs234930. doi: 10.1242/jcs.234930.
7
The Atypical MAP Kinase ErkB Transmits Distinct Chemotactic Signals through a Core Signaling Module.
Dev Cell. 2019 Feb 25;48(4):491-505.e9. doi: 10.1016/j.devcel.2018.12.001. Epub 2019 Jan 3.
8
Association of mSin1 with mTORC2 Ras and Akt reveals a crucial domain on mSin1 involved in Akt phosphorylation.
Oncotarget. 2017 Jun 28;8(38):63392-63404. doi: 10.18632/oncotarget.18818. eCollection 2017 Sep 8.
9
The small GTPases Ras and Rap1 bind to and control TORC2 activity.
Sci Rep. 2016 May 13;6:25823. doi: 10.1038/srep25823.
10
The TORC2 component, Sin1, controls migration of anterior mesendoderm during zebrafish gastrulation.
PLoS One. 2015 Feb 24;10(2):e0118474. doi: 10.1371/journal.pone.0118474. eCollection 2015.

本文引用的文献

3
G protein signaling events are activated at the leading edge of chemotactic cells.
Cell. 1998 Oct 2;95(1):81-91. doi: 10.1016/s0092-8674(00)81784-5.
6
cGMP as second messenger during Dictyostelium chemotaxis.
FEBS Lett. 1997 Jun 23;410(1):25-8. doi: 10.1016/s0014-5793(97)00416-x.
7
Dictyostelium RasG is required for normal motility and cytokinesis, but not growth.
J Cell Biol. 1997 Aug 11;138(3):605-14. doi: 10.1083/jcb.138.3.605.
8
Regulation of actin polymerization in cell-free systems by GTPgammaS and Cdc42.
J Cell Biol. 1997 Jul 28;138(2):363-74. doi: 10.1083/jcb.138.2.363.
9
Dictyostelium development in the absence of cAMP.
Science. 1997 Jul 11;277(5323):251-4. doi: 10.1126/science.277.5323.251.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验