调控网络和关键因素促进胚胎发生过程中被编程细胞死亡
Journal of integrative plant biology
|November 8, 2024
概括
这项研究揭示了植物编程细胞死亡 (PCD) 中的关键分子参与者. 我们确定了一个基因和通路网络,包括由蛋白酶NtCP14调节的活性氧物种 (ROS),为植物发育提供了新的见解.
科学领域:
- 植物分子生物学 植物分子生物学
- 发育生物学是发展生物学.
- 细胞死亡机制 细胞死亡机制
背景情况:
- 编程细胞死亡 (PCD) 对植物发育至关重要,但由于技术挑战,其调节机制尚不清楚.
- 蛋白酶NtCP14此前已被确定为烟草胚胎悬浮剂中PCD的触发物.
研究的目的:
- 在同步的双细胞胚胎中研究调节NtCP14触发PCD的分子网络.
- 确定有关早期悬浮剂PCD的关键监管因素和下游目标.
主要方法:
- 对经过PCD的分离双细胞前胚胎进行比较转录组分析.
- 生物信息分析用于探索调控网络并识别候选基因.
主要成果:
- 确定了植物激素,,微管组织,免疫力,SNARE蛋白质,lncRNAs和替代拼接作为早期悬浮体PCD的关键因素.
- 观察到抗氧化剂基因表达的减少和活性氧物种 (ROS) 水平的增加,这表明ROS信号传递的作用.
- 突出了五个基因作为NtCP14潜在的直接下游目标.
结论:
- 该研究概述了植物中蛋白酶触发PCD的分子网络.
- 为了解植物PCD和确定治疗点提供了宝贵的资源.
- 表明ROS信号传递对于启动NtCP14诱导的PCD至关重要.
更多相关视频
09:07Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation
Published on: June 21, 2016
8.2K
09:51Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress
Published on: May 7, 2014
15.2K
相关概念视频
Molecular Factors Affecting Cell Division
3.0K
Several external and internal factors influence the initiation and inhibition of cell division. For instance, the death of nearby cells or the release of human growth hormone (hGH) promotes cell division. In contrast, lack of hGH or crowding of cells can inhibit cell division.
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
3.0K
Overview of Cell Death
7.1K
Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
7.1K
The Cell Cycle Control System
2.6K
The cell cycle regulation directs how a cell proceeds from one phase to the next and begins mitosis. The cell cycle control system includes intracellular regulatory molecules and external triggers. They provide "stop" or "advance" signals and operate at specific cell cycle stages termed checkpoints to ensure that a particular process is completed before the cell advances to the next phase.
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
2.6K
Negative Regulator Molecules
35.2K
Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
35.2K
The Extrinsic Apoptotic Pathway
6.3K
The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
6.3K
Regulation of the Unfolded Protein Response
2.4K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.4K
