Suppr超能文献

Par-1和Tau调节果蝇卵母细胞中微管的前后梯度。

Par-1 and Tau regulate the anterior-posterior gradient of microtubules in Drosophila oocytes.

作者信息

Tian Ai-Guo, Deng Wu-Min

机构信息

Department of Biological Science, Florida State University, Tallahassee, FL 32306-4370, USA.

出版信息

Dev Biol. 2009 Mar 15;327(2):458-64. doi: 10.1016/j.ydbio.2008.12.031. Epub 2009 Jan 3.

Abstract

The formation of an anterior-posterior (AP) gradient of microtubules in Drosophila oocytes is essential for specification of the AP axis. Proper microtubule organization in the oocyte requires the function of serine/threonine kinase Par-1. The N1S isoform of Par-1 is enriched at the posterior cortex of the oocyte from stage 7 of oogenesis. Here we report that posterior restriction of Par-1 (N1S) kinase activity is critical for microtubule AP gradient formation. Egg chambers with excessive and ectopic Par-1 (N1S) kinase activity in the germline cells display phenotypes similar to those of egg chambers treated with the microtubule-depolymerizing drug colcemid: depolymerization of microtubules in the oocyte and disruption of oocyte nucleus localization. A phosphorylation target of Par-1, the microtubule-associated protein Tau, is also involved in oocyte polarity formation, and overexpression of Tau alleviates the phenotypes caused by ectopic Par-1 (N1S) kinase activity, suggesting that Par-1 regulates oocyte polarity at least partly through Tau. Our findings reveal that maintaining proper levels of Par-1 at correct position in the oocyte is key to oocyte polarity formation and that the conserved role of Par-1 and Tau is crucial for the establishment of an AP gradient of microtubules and for AP axis specification.

摘要

果蝇卵母细胞中微管前后(AP)梯度的形成对于AP轴的特化至关重要。卵母细胞中微管的正确组织需要丝氨酸/苏氨酸激酶Par-1的功能。从卵子发生的第7阶段开始,Par-1的N1S亚型在卵母细胞的后皮质富集。我们在此报告,Par-1(N1S)激酶活性的后向限制对于微管AP梯度的形成至关重要。生殖系细胞中具有过量和异位Par-1(N1S)激酶活性的卵室表现出与用微管解聚药物秋水仙酰胺处理的卵室相似的表型:卵母细胞中微管的解聚和卵母细胞核定位的破坏。Par-1的磷酸化靶点、微管相关蛋白Tau也参与卵母细胞极性的形成,并且Tau的过表达减轻了由异位Par-1(N1S)激酶活性引起的表型,这表明Par-1至少部分地通过Tau调节卵母细胞极性。我们的研究结果表明,在卵母细胞的正确位置维持适当水平的Par-1是卵母细胞极性形成的关键,并且Par-1和Tau的保守作用对于微管AP梯度的建立和AP轴的特化至关重要。

相似文献

1
Par-1 and Tau regulate the anterior-posterior gradient of microtubules in Drosophila oocytes.
Dev Biol. 2009 Mar 15;327(2):458-64. doi: 10.1016/j.ydbio.2008.12.031. Epub 2009 Jan 3.
3
Lgl and its phosphorylation by aPKC regulate oocyte polarity formation in Drosophila.
Development. 2008 Feb;135(3):463-71. doi: 10.1242/dev.016253. Epub 2007 Dec 19.
4
Bazooka is required for polarisation of the Drosophila anterior-posterior axis.
Development. 2010 May;137(10):1765-73. doi: 10.1242/dev.045807.
5
Drosophila par-1 is required for oocyte differentiation and microtubule organization.
Curr Biol. 2001 Jan 23;11(2):75-87. doi: 10.1016/s0960-9822(01)00027-6.
7
PAR-1 is required for the maintenance of oocyte fate in Drosophila.
Development. 2001 Apr;128(7):1201-9. doi: 10.1242/dev.128.7.1201.
9
Bazooka and atypical protein kinase C are required to regulate oocyte differentiation in the Drosophila ovary.
Proc Natl Acad Sci U S A. 2001 Dec 4;98(25):14475-80. doi: 10.1073/pnas.261565198.
10
The CPEB translational regulator, Orb, functions together with Par proteins to polarize the Drosophila oocyte.
PLoS Genet. 2019 Mar 13;15(3):e1008012. doi: 10.1371/journal.pgen.1008012. eCollection 2019 Mar.

引用本文的文献

1
Gastrodin blocks neural stem cell differentiation into glial cells mediated by kainic acid.
Neural Regen Res. 2012 Apr 25;7(12):891-5. doi: 10.3969/j.issn.1673-5374.2012.12.002.
3
Efficient EGFR signaling and dorsal-ventral axis patterning requires syntaxin dependent Gurken trafficking.
Dev Biol. 2013 Jan 15;373(2):349-58. doi: 10.1016/j.ydbio.2012.10.029. Epub 2012 Nov 2.
4
Drosophila models of tauopathies: what have we learned?
Int J Alzheimers Dis. 2012;2012:970980. doi: 10.1155/2012/970980. Epub 2012 Jun 4.
6
The power and richness of modelling tauopathies in Drosophila.
Mol Neurobiol. 2011 Aug;44(1):122-33. doi: 10.1007/s12035-011-8193-1. Epub 2011 Jun 17.
7
Loss of Par-1a/MARK3/C-TAK1 kinase leads to reduced adiposity, resistance to hepatic steatosis, and defective gluconeogenesis.
Mol Cell Biol. 2010 Nov;30(21):5043-56. doi: 10.1128/MCB.01472-09. Epub 2010 Aug 23.
8
Bazooka is required for polarisation of the Drosophila anterior-posterior axis.
Development. 2010 May;137(10):1765-73. doi: 10.1242/dev.045807.
9
Alzheimer's disease and tauopathy studies in flies and worms.
Neurobiol Dis. 2010 Oct;40(1):21-8. doi: 10.1016/j.nbd.2010.03.007. Epub 2010 Mar 17.
10
Bazooka regulates microtubule organization and spatial restriction of germ plasm assembly in the Drosophila oocyte.
Dev Biol. 2010 Apr 15;340(2):528-38. doi: 10.1016/j.ydbio.2010.02.006. Epub 2010 Feb 10.

本文引用的文献

2
Lgl and its phosphorylation by aPKC regulate oocyte polarity formation in Drosophila.
Development. 2008 Feb;135(3):463-71. doi: 10.1242/dev.016253. Epub 2007 Dec 19.
3
Salvador-warts-hippo signaling promotes Drosophila posterior follicle cell maturation downstream of notch.
Curr Biol. 2007 Nov 6;17(21):1864-70. doi: 10.1016/j.cub.2007.09.049. Epub 2007 Oct 25.
4
The salvador-warts-hippo pathway is required for epithelial proliferation and axis specification in Drosophila.
Curr Biol. 2007 Nov 6;17(21):1871-8. doi: 10.1016/j.cub.2007.09.062. Epub 2007 Oct 25.
6
The centrosome-nucleus complex and microtubule organization in the Drosophila oocyte.
Development. 2006 Jan;133(1):129-39. doi: 10.1242/dev.02179. Epub 2005 Nov 30.

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