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Brief guide to assays for measuring health parameters using Caenorhabditis elegans 用秀丽隐杆线虫测定健康参数的试验指南。
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-26 DOI: 10.1016/j.mocell.2025.100233
Seungjae Hwang, Jongsun Lee, Seung-Jae V. Lee
Assessing health parameters is essential for understanding the decline of physiological functions during aging. The nematode Caenorhabditis elegans serves as a powerful model in aging research. This paper introduces representative methods for evaluating health parameters using C. elegans and provides quantitative indicators of functional declines during aging. This manuscript will be useful for researchers unfamiliar with healthspan studies using C. elegans and may help perform physiological experiments for healthy aging.
评估健康参数是了解衰老过程中生理功能下降的必要条件。秀丽隐杆线虫是衰老研究中一个强有力的模型。介绍了秀丽隐杆线虫健康参数评价的代表性方法,给出了衰老过程中功能衰退的定量指标。这篇论文将对不熟悉秀丽隐杆线虫健康寿命研究的研究人员有用,并可能有助于进行健康衰老的生理实验。
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引用次数: 0
Cover and caption 封面及标题
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-21 DOI: 10.1016/S1016-8478(25)00052-4
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引用次数: 0
Editorial Board Members/Copyright 编辑委员会成员/版权
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-21 DOI: 10.1016/S1016-8478(25)00053-6
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引用次数: 0
MicroRNA-196a increases apoptosis in B cells through downregulation of FOXO1 MicroRNA-196a通过下调fox01增加B细胞凋亡。
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-20 DOI: 10.1016/j.mocell.2025.100223
Soyoung Kim , Mina Han , Hyun Ju Hwang , Young-Ho Ahn , Ho Joon Im , Sang-Hyun Hwang , Kyung-Nam Koh , Nayoung Kim
MicroRNAs (miRNAs) are key regulators of cancer pathogenesis, and their expression is often dysregulated in cancer cells. The role of miR-196a-5p has been investigated in various types of cancers. However, it is relatively less understood in B-cell malignancies. This study aimed to investigate the role of miR-196a-5p in B cells by using a human diffuse large B-cell lymphoma cell line, SU-DHL-6, and mouse B lymphocytes. The enforced expression of miR-196a in SU-DHL-6 cells increased daunorubicin-mediated apoptosis. Luciferase assay revealed that FOXO1 was a direct target of miR-196a-5p in SU-DHL-6 cells. The mRNA and protein expression of FOXO1 was downregulated in miR-196a-overexpressing SU-DHL-6 cells. In addition, miR-196a-5p was highly expressed in mouse bone marrow cells, compared with that of splenic B cells, and FOXO1 expression was negatively correlated with miR-196a-5p level. miR-196a-5p was upregulated by B-cell receptor stimulation, which was inversely correlated with FOXO1 expression in splenic B cells. Apoptosis was increased when miR-196a-5p was upregulated in murine primary B cells. These results identify miR-196a-5p as a post-transcriptional regulator of FOXO1 and indicate its importance in regulating B-cell malignancies and activation.
MicroRNAs (miRNAs)是癌症发病的关键调控因子,其表达在癌细胞中经常失调。miR-196a-5p在各种类型的癌症中的作用已被研究,但在b细胞恶性肿瘤中的作用相对较少。本研究旨在通过人弥漫性大B细胞淋巴瘤(DLBCL)细胞系、SU-DHL-6和小鼠B淋巴细胞来研究miR-196a-5p在B细胞中的作用。miR-196a在SU-DHL-6细胞中的强制表达增加了柔红霉素介导的细胞凋亡。荧光素酶检测显示FOXO1是SU-DHL-6细胞中miR-196a-5p的直接靶点。过表达mir -196a的SU-DHL-6细胞中FOXO1 mRNA和蛋白表达下调。此外,miR-196a-5p在小鼠骨髓(BM)细胞中高表达,与脾(SP) B细胞相比,FOXO1表达与miR-196a-5p水平呈负相关。miR-196a-5p在B细胞受体(BCR)刺激下上调,与SP B细胞中FOXO1的表达呈负相关。上调miR-196a-5p可增加小鼠原代B细胞的凋亡。这些结果确定了miR-196a-5p是fox01的转录后调节因子,并表明其在调节B细胞恶性肿瘤和激活中的重要性。
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引用次数: 0
A novel high-throughput single-molecule technique DNA curtain: Applications for DNA metabolism 一种新的高通量单分子技术DNA幕:在DNA代谢中的应用。
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-20 DOI: 10.1016/j.mocell.2025.100224
Soyeong An , Youngseo Kim , Ja Yil Lee
The advancement of single-molecule imaging techniques has significantly enhanced our understanding of biomolecular reactions and cellular processes that remain obscured in ensemble measurements. In particular, DNA curtains are high-throughput hybrid methods integrating total internal reflection fluorescence microscopy, lipid fluidity, microfluidics, and nano-fabrication, enabling the direct visualization of protein-DNA interactions in real time. The techniques have emerged as powerful tools for probing molecular dynamics of diverse DNA metabolic processes, including DNA damage repair and chromatin dynamics. This review not only highlights recent applications of DNA curtain techniques for elucidating mechanisms underlying DNA damage repair and chromatin dynamics, but also shows how DNA curtain techniques have provided novel insights into the interplay between DNA metabolic processes in the chromatin context.
单分子成像技术的进步大大提高了我们对生物分子反应和细胞过程的理解,这些反应和细胞过程在集合测量中仍然模糊不清。特别是,DNA窗帘是一种高通量混合方法,集成了全内反射荧光显微镜、脂质流动性、微流体和纳米制造,能够实时直接可视化蛋白质-DNA相互作用。这些技术已经成为探测各种DNA代谢过程的分子动力学的有力工具,包括DNA损伤修复和染色质动力学。这篇综述不仅强调了DNA幕技术在阐明DNA损伤修复和染色质动力学机制方面的最新应用,而且还展示了DNA幕技术如何为染色质背景下DNA代谢过程之间的相互作用提供了新的见解。
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引用次数: 0
Effects of heterozygous SMG1 mutations on nonsense-mediated mRNA decay in human pluripotent stem cell model 杂合SMG1突变对人多能干细胞模型中无义介导的mRNA衰变的影响。
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-20 DOI: 10.1016/j.mocell.2025.100225
Chanyoung Lee , Jin Sook Lee , Yejin Kwon , Aeri Shin , Tae Yeong Jeong , Jiyun Yang , Jung Woo Hwang , Hyeong-In Kim , Hee-Jung Choi , Yoon Ki Kim , Murim Choi , Kyoungmi Kim , Woong Sun , Jong-Hee Chae
Nonsense-mediated mRNA decay (NMD) eliminates transcripts containing premature termination codons, thereby preventing errors in protein synthesis. Serine/threonine-protein kinase SMG1 is a crucial kinase for NMD response, interacting with other regulatory proteins such as SMG8 and SMG9. We identified a de novo heterozygous variant in SMG1 p.Gln2398Glu (c.7192C>G) in a patient with global developmental delay, facial dysmorphism, and oculomotor apraxia. Thus, stem cell models with SMG1 mutations using gene editing technology were established to address the functional consequences of this mutation. While mutations causing the reduction in SMG1 gene dosage by alterations in splicing (c.7192_7194delinsGAA; GAA/+) or frameshift (c.4331_4337del; KO/+) led to a mild but significant reduction of NMD activity, NMD activity was not altered in cells with the SMG1 GAG/+ mutation. Furthermore, cortical organoids from hPSCGAA/+ exhibited size reduction compared with the control (CTL) or GAG/+, suggesting that reduced NMD activity can affect nervous system development. These findings suggest that hypomorphic SMG1 mutations can cause reduced NMD activity and subsequent biological responses, while the mutation found in the patient alone may not be sufficient to induce pathological symptoms.
无义介导的mRNA衰变(NMD)消除了含有过早终止密码子(ptc)的转录本,从而防止了蛋白质合成中的错误。丝氨酸/苏氨酸蛋白激酶SMG1是NMD应答的关键激酶,与其他调节蛋白如SMG8和SMG9相互作用。我们在一名患有全面发育迟缓、面部畸形和动眼失用症的患者中发现了SMG1 p.Gln2398Glu (c.7192C>G)的新杂合变异。因此,利用基因编辑技术建立SMG1突变干细胞模型,以解决该突变的功能后果。而突变通过剪接的改变导致SMG1基因剂量的减少(c.7192_7194delinsGAA;GAA/+)或移码(c. 4331_437del;KO/+)导致NMD活性轻度但显著降低,SMG1 GAG/+突变细胞的NMD活性未发生改变。此外,与对照(CTL)或GAG/+相比,来自hPSCGAA/+的皮质类器官显示出体积减小,这表明NMD活性降低可以影响神经系统的发育。这些发现表明,SMG1亚型突变可导致NMD活性降低和随后的生物反应,而仅在患者中发现的突变可能不足以诱导病理症状。
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引用次数: 0
SimpleViz: A user-friendly, web-based tool for publication-ready data visualization in bioinformatics SimpleViz:一个用户友好的,基于web的工具,用于生物信息学中出版就绪的数据可视化。
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-05-08 DOI: 10.1016/j.mocell.2025.100222
Byeong Seob Oh , Juhee Kim , Minjeong Kwon , Jiwon Bang , Kwang-Jun Lee , Eun-Jin Lee , Yong-Joon Cho
Large-scale datasets are central to bioinformatics research, creating a demand for intuitive visualization tools that transform complex data into accessible graphics. Existing visualization software often comes with high costs or requires coding expertise, limiting accessibility for many researchers. To address this gap, we introduce SimpleViz, a free, web-based platform that enables the creation of professional-quality figures without the need for programming skills. SimpleViz offers gene-level analysis of RNA-seq data and core visualization types such as box/violin/dot plots, volcano plots, principal component analysis plots, and heatmaps, with extensive customization options for detailed adjustments and built-in statistical comparisons. Developed on a Shiny interface, SimpleViz simplifies the process of data upload, visualization generation, and customization, ensuring that users can produce tailored visuals suited for publication. With plans for continuous improvement based on user feedback, SimpleViz provides an adaptable, accessible solution that meets evolving data analysis needs in biomedical research.
大规模数据集是生物信息学研究的核心,它创造了对直观可视化工具的需求,这些工具可以将复杂的数据转换为可访问的图形。现有的可视化软件通常成本很高,或者需要编码专业知识,限制了许多研究人员的可访问性。为了解决这一差距,我们推出了SimpleViz,这是一个免费的基于web的平台,可以在不需要编程技能的情况下创建专业质量的图形。SimpleViz提供RNA-seq数据的基因水平分析和核心可视化类型,如盒/小提琴/点阵图,火山图,PCA图和热图,具有广泛的定制选项,可进行详细调整和内置统计比较。SimpleViz基于Shiny界面开发,简化了数据上传、可视化生成和自定义的过程,确保用户可以生成适合发布的定制视觉效果。SimpleViz计划根据用户反馈进行持续改进,提供了一个适应性强、易于访问的解决方案,以满足生物医学研究中不断发展的数据分析需求。
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引用次数: 0
Open-source software utilization for zebrafish embryos behavior test 利用开源软件进行斑马鱼胚胎行为测试
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-25 DOI: 10.1016/j.mocell.2025.100221
Thilini Ranasinghe , Seon-Heui Cha
This work described simple methods for measuring locomotive activity using open-source software, ImageJ1.54fFiji, and VirtualDub2. The significance of animal behavior is a mirror of brain activity, which can give information implicated with neurological diseases. Commercial behavioral analysis software frequently needs expertise and expenses high costs due to equip a specific instrument to use of software, thereby encouraging a trend toward open-source alternatives that are both accessible and effective. Here, we explained how to convert video format, measure movement, and produce useful locomotive parameters to aid in the assessment of zebrafish embryos. This method could be easily translated for use in other model systems. This methodology seeks to streamline behavioral quantification in research contexts, encouraging broader research aspects.
这项工作描述了使用开源软件ImageJ1.54fFiji和VirtualDub2测量机车活动的简单方法。动物行为的意义是大脑活动的一面镜子,它可以提供与神经系统疾病有关的信息。商业行为分析软件经常需要专业知识,并且由于配备特定的工具来使用软件而花费高昂的成本,因此鼓励了向可访问且有效的开源替代方案发展的趋势。在这里,我们解释了如何转换视频格式,测量运动,并产生有用的机车参数,以帮助评估斑马鱼胚胎。这种方法可以很容易地转换为用于其他模型系统。这种方法旨在简化研究背景下的行为量化,鼓励更广泛的研究方面。
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Cover and caption 封面及标题
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-21 DOI: 10.1016/S1016-8478(25)00041-X
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Editorial Board Members/Copyright 编辑委员会成员/版权
IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-21 DOI: 10.1016/S1016-8478(25)00043-3
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引用次数: 0
期刊
Molecules and Cells
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