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一种假定的O-连接β-N-乙酰葡糖胺转移酶对丝状蓝细菌点状念珠藻中藻殖段的发育和运动至关重要。

A Putative O-Linked β--Acetylglucosamine Transferase Is Essential for Hormogonium Development and Motility in the Filamentous Cyanobacterium Nostoc punctiforme.

作者信息

Khayatan Behzad, Bains Divleen K, Cheng Monica H, Cho Ye Won, Huynh Jessica, Kim Rachelle, Omoruyi Osagie H, Pantoja Adriana P, Park Jun Sang, Peng Julia K, Splitt Samantha D, Tian Mason Y, Risser Douglas D

机构信息

Department of Biology, University of the Pacific, Stockton, California, USA.

Department of Biology, University of the Pacific, Stockton, California, USA

出版信息

J Bacteriol. 2017 Apr 11;199(9). doi: 10.1128/JB.00075-17. Print 2017 May 1.

Abstract

Most species of filamentous cyanobacteria are capable of gliding motility, likely via a conserved type IV pilus-like system that may also secrete a motility-associated polysaccharide. In a subset of these organisms, motility is achieved only after the transient differentiation of hormogonia, which are specialized filaments that enter a nongrowth state dedicated to motility. Despite the fundamental importance of hormogonia to the life cycles of many filamentous cyanobacteria, the molecular regulation of hormogonium development is largely undefined. To systematically identify genes essential for hormogonium development and motility in the model heterocyst-forming filamentous cyanobacterium , a forward genetic screen was employed. The first gene identified using this screen, designated , encodes a putative O-linked β--acetylglucosamine transferase (OGT). The deletion of abolished motility, while ectopic expression of induced hormogonium development even under hormogonium-repressing conditions. Transcription of is rapidly upregulated (1 h) following hormogonium induction, and an OgtA-GFPuv fusion protein localized to the cytoplasm. In developing hormogonia, accumulation of PilA but not HmpD is dependent on Reverse transcription-quantitative PCR (RT-qPCR) analysis indicated equivalent levels of transcript in the wild-type and Δ mutant strains, while a reporter construct consisting of the intergenic region in the 5' direction of fused to produced lower levels of fluorescence in the Δ mutant strain than in the wild type. The production of hormogonium polysaccharide in the Δ mutant strain is reduced compared to that in the wild type but comparable to that in a deletion strain. Collectively, these results imply that -GlcNAc protein modification regulates the accumulation of PilA via a posttranscriptional mechanism in developing hormogonia. Filamentous cyanobacteria are among the most developmentally complex prokaryotes. Species such as develop an array of cell types, including nitrogen-fixing heterocysts, spore-like akinetes, and motile hormogonia, that function in dispersal as well as the establishment of nitrogen-fixing symbioses with plants and fungi. These symbioses are major contributors to global nitrogen fixation. Despite the fundamental importance of hormogonia to the life cycle of filamentous cyanobacteria and the establishment of symbioses, the molecular regulation of hormogonium development is largely undefined. We employed a genetic screen to identify genes essential for hormogonium development and motility in The first gene identified using this screen encodes a eukaryotic-like O-linked β--acetylglucosamine transferase that is required for accumulation of PilA in hormogonia.

摘要

大多数丝状蓝细菌物种都具有滑行运动能力,可能是通过一种保守的IV型菌毛样系统,该系统也可能分泌与运动相关的多糖。在这些生物体的一个亚群中,只有在异形胞短暂分化后才能实现运动,异形胞是进入专门用于运动的非生长状态的特殊丝状体。尽管异形胞对许多丝状蓝细菌的生命周期至关重要,但异形胞发育的分子调控在很大程度上尚不清楚。为了系统地鉴定模式异形胞形成丝状蓝细菌中异形胞发育和运动所必需的基因,我们采用了正向遗传筛选。使用该筛选鉴定出的第一个基因,命名为 ,编码一种推定的O-连接β-N-乙酰葡糖胺转移酶(OGT)。 的缺失消除了运动能力,而即使在抑制异形胞的条件下, 的异位表达也诱导了异形胞的发育。异形胞诱导后1小时, 的转录迅速上调,并且OgtA-GFPuv融合蛋白定位于细胞质。在发育中的异形胞中,PilA的积累而非HmpD的积累依赖于 。逆转录定量PCR(RT-qPCR)分析表明野生型和Δ突变体菌株中 转录本水平相当,而由 5' 方向的基因间区域与 融合组成的报告构建体在Δ突变体菌株中产生的荧光水平低于野生型。与野生型相比,Δ突变体菌株中异形胞多糖的产生减少,但与 缺失菌株中的相当。总的来说,这些结果表明,在发育中的异形胞中,-GlcNAc蛋白修饰通过转录后机制调节PilA的积累。丝状蓝细菌是发育最复杂的原核生物之一。诸如 等物种会发育出一系列细胞类型,包括固氮异形胞、孢子样厚壁孢子和运动性异形胞,它们在扩散以及与植物和真菌建立固氮共生关系中发挥作用。这些共生关系是全球固氮的主要贡献者。尽管异形胞对丝状蓝细菌的生命周期和共生关系的建立至关重要,但异形胞发育的分子调控在很大程度上尚不清楚。我们采用遗传筛选来鉴定 中异形胞发育和运动所必需的基因。使用该筛选鉴定出的第一个基因编码一种真核样O-连接β-N-乙酰葡糖胺转移酶,它是异形胞中PilA积累所必需的。

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