Regulation of septum formation by the SIN, MOR and BUD modules

SIN、MOR 和 BUD 模块对隔膜形成的调节

• 批准号: 227531368
• 负责人: Privatdozent Dr. Stephan Seiler
• 金额: --
• 依托单位国家: 德国
• 项目类别: Research Grants
• 财政年份: 2012
• 资助国家: 德国
• 起止时间: 2011-12-31 至 2018-12-31
• 项目状态: 已结题
• 来源: https://gepris.dfg.de/gepris/projekt/227531368?language=en
• 关键词: Regulation; septum; formation; SIN; MOR

Fungi are outstanding models for the analysis of fundamental mechanisms underlying growth and differentiation. They represent the second largest group of eukaryotic organisms on earth and are recognized for their importance in ecology, biotechnology and their role as plant and human pathogens. Most fungi form mycelial colonies that consist of networks of branched hyphae, grow by apical extension and are compartmentalized by perforated cross-walls, called septa. This segmentation of communicating cell units is the basis for the morphological complexity achieved by the fungi and for the success of the fungal kingdom. Despite the importance of septation for fungal growth, proliferation and differentiation, our understanding of septum formation and its regulation is highly fragmentary. Based on our preliminary and published data on the interplay between two NDR kinase cascades and the BUD3-BUD4 landmark complex, we will determine (i) the composition and regulation of the septation initiation network, (ii) its potential connection with microtubule organization and nuclear behavior, (iii) the actin dynamics during septum placement and formation of the contractile actmyosin ring, (iv) the cross-regulation of the SIN/MOR networks, and (v) characterize candidate targets of the SIN/MOR kinases during septation initiation and termination. Using classical and molecular genetic approaches along with kinase and Rho GTPase biochemistry and life-microscopy we will dissect the mechanisms that control septation in a model mold. This project will provide insight into the fundamental mechanisms controlling growth and differentiation of multinucleated eukaryotic cells.

真菌是分析生长和分化基本机制的杰出模型。它们是地球上第二大真核生物群，在生态学、生物技术以及作为植物和人类病原体的作用方面具有重要意义。大多数真菌形成菌丝菌落，菌丝菌落由分枝菌丝网络组成，通过顶端延伸生长，并被称为隔的穿孔交叉壁分隔开。这种通讯细胞单位的分割是真菌实现形态复杂性和真菌王国成功的基础。尽管分隔对真菌生长、增殖和分化具有重要意义，但我们对分隔形成及其调控的理解是高度不完整的。基于我们关于两个NDR激酶级联与BUD3-BUD4里程碑式复合物之间相互作用的初步和已发表的数据，我们将确定(i)分隔起始网络的组成和调控，（ii）其与微管组织和核行为的潜在联系，（iii）间隔放置和收缩actimyosin环形成过程中的肌动蛋白动力学，（iv） SIN/MOR网络的交叉调控。(v)在分离起始和终止过程中表征SIN/MOR激酶的候选靶点。使用经典和分子遗传学方法以及激酶和Rho GTPase生物化学和生命显微镜，我们将剖析控制模型霉菌分离的机制。本项目将深入研究多核真核细胞生长和分化的基本机制。