Molecular fingerprints of cell size sensing and mating type differentiation in pennate diatoms

IF 8.1 1区 生物学 Q1 PLANT SCIENCES New Phytologist Pub Date : 2024-12-08 DOI:10.1111/nph.20334
Darja Belišová, Gust Bilcke, Sien Audoor, Sofie D'hondt, Lieven De Veylder, Klaas Vandepoele, Wim Vyverman
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Abstract

  • A unique cell size-sensing mechanism is at the heart of the life cycle of diatoms. During population growth, cell size decreases until a sexual size threshold (SST) is reached, below which cells become sexually competent. In most pennate diatoms, the two mating types undergo biochemical and behavioral differentiation below the SST, although the molecular pathways underlying their size-dependent maturation remain unknown.
  • Here, we developed a method to shorten the generation time of Cylindrotheca closterium through single-cell microsurgery, enabling the transcriptomic comparison of genetically identical large and undifferentiated cells with small, sexually competent cells for six different genotypes.
  • We identified 21 genes upregulated in small cells regardless of their mating type, revealing how cells undergo specific transcriptional reprogramming when passing the SST. Furthermore, we revealed a size-regulated gene cluster with three mating type-specific genes susceptible to sex-inducing pheromones. In addition, comparative transcriptomics confirmed the shared mating type specificity of Mating-type Related Minus 2 homologs in three pennate diatoms, suggesting them to be part of a conserved partner recognition mechanism.
  • This study sheds light on how diatoms acquire sexual competence in a strictly size-dependent manner, revealing a complex machinery underlying size-dependent maturation, mating behavior, and heterothally in pennate diatoms.
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pennate硅藻细胞大小感知和交配类型分化的分子指纹图谱
一种独特的细胞大小感应机制是硅藻生命周期的核心。在种群生长过程中,细胞大小逐渐减小,直到达到有性大小阈值(SST),低于该阈值细胞就具有性能力。在大多数pennate硅藻中,两种交配类型在低于海温的情况下经历生化和行为分化,尽管其大小依赖性成熟的分子途径尚不清楚。在这里,我们开发了一种方法,通过单细胞显微手术来缩短圆柱形膜绦虫的产生时间,使六种不同基因型的遗传相同的大细胞和未分化细胞与小细胞的转录组学比较成为可能。我们发现了21个基因在小细胞中上调,无论其交配类型如何,揭示了细胞在传递SST时如何进行特异性转录重编程。此外,我们发现了一个大小调控的基因簇,其中有三个交配类型特异性基因对性诱导信息素敏感。此外,比较转录组学证实了三种pennate硅藻的共同交配型特异性,表明它们是保守伴侣识别机制的一部分。这项研究揭示了硅藻是如何以严格依赖于大小的方式获得性能力的,揭示了pennate硅藻中大小依赖的成熟、交配行为和异源性的复杂机制。
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
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