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Expression of the siss-1 gene in C. elegans. siss1基因在秀丽隐杆线虫中的表达。
Pub Date : 2026-02-02 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001976
Marine Barsegyan, Cheryl Van Buskirk

C. elegans SISS-1 is an Epidermal Growth Factor (EGF) family ligand that signals from damaged cells to sleep-promoting neurons during s tress- i nduced s leep (SIS). Damage to a range of tissues can trigger SIS, and we reasoned that siss-1 should be widely expressed. Here we investigate siss-1 expression using both endogenous and transgenic fluorescent reporters. Our endogenous reporter reveals siss-1 expression in the pharynx, gut, rectal gland, vulval muscles, and a subset of neurons. Our transgenic reporters reveal expression in additional cell types including the distal tip cell of the migrating gonad and vulF cells of the developing vulva. This expression is specific relative to our expectation and suggests that not all tissues are capable of signaling to sleep neurons.

秀丽隐杆线虫SISS-1是一种表皮生长因子(EGF)家族配体,在应激诱导的睡眠(SIS)过程中,从受损细胞向促进睡眠的神经元发出信号。对一系列组织的损伤可以触发SIS,我们推断siss-1应该广泛表达。在这里,我们使用内源性和转基因荧光报告基因来研究siss-1的表达。我们的内源性报告显示,siss-1在咽、肠、直肠腺、外阴肌肉和一部分神经元中表达。我们的转基因报告显示在其他细胞类型中表达,包括迁移性腺的远端细胞和发育中的外阴的外阴细胞。这种表达相对于我们的预期是特定的,并表明并非所有组织都能够向睡眠神经元发出信号。
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引用次数: 0
Assay of Ds2 Transposition Activity in the Maize W22. 玉米W22中Ds2转位活性的测定
Pub Date : 2026-02-02 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001902
Harpreet Kaur, Matthew Bacchus, Lilly Horowitz, Caroline Larow, Vedant Rawat, Dafang Wang

Ds elements are non-autonomous DNA transposons requiring Ac transposase for mobility. From the 39 Ds2 elements reported in B73, we identified 38 Ds2 homologous elements in the W22, 30 of which retained intact terminal inverted repeats and target site duplications. PCR-based excision assays on 19 loci in embryos and leaves revealed the majority are immobile; only Ds2-23 showed suggestive somatic transposition. Targeted bisulfite sequencing revealed that while Ac reduces methylation, absolute levels remain stable and do not correspond to the varied transposition activities. This suggests structural integrity or DNA methylation alone does not predict Ds2 transposition variation in W22.

Ds元素是非自主的DNA转座子,需要Ac转座酶来实现迁移。从B73报道的39个Ds2元件中,我们在W22中鉴定出38个Ds2同源元件,其中30个保留了完整的末端反向重复和目标位点重复。对胚胎和叶片中的19个基因座进行pcr切除分析,结果显示大多数基因座是不动的;只有Ds2-23显示提示体细胞移位。靶向亚硫酸酯测序显示,虽然Ac降低甲基化,但绝对水平保持稳定,不对应于不同的转位活性。这表明结构完整性或DNA甲基化本身不能预测W22的Ds2转位变异。
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引用次数: 0
Tocopherol Profile Variations of Soybean World Mini-Core Collection Accessions Grown in Hokkaido. 北海道大豆世界小核心种质的生育酚谱变化。
Pub Date : 2026-01-27 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001813
Maria Stefanie Dwiyanti

Tocopherols (vitamin E) are lipid-soluble antioxidants, with α-tocopherol having the highest vitamin E activity. Soybean seed is a major source of tocopherols. Therefore, improving seed tocopherol content is a key breeding objective. Thirty-eight accessions from the soybean world mini-core collection were evaluated in 2019 and 2022 growing seasons. Four accessions carried a high α-tocopherol associated allele at S09_44341929 but they did not reach the high α-tocopherol levels of cultivar KAS, likely due to cooler seed-filling conditions. Moshido Gong 502 and 503 showed low total tocopherol content in both seasons, making them promising resources for investigating genetic regulation of tocopherol biosynthesis.

生育酚(维生素E)是脂溶性抗氧化剂,α-生育酚具有最高的维生素E活性。大豆种子是生育酚的主要来源。因此,提高种子生育酚含量是育种的关键目标。对2019年和2022年两个生长季的38份大豆世界小核心种质进行了评价。4个品种携带高α-生育酚相关等位基因S09_44341929,但未达到KAS的高α-生育酚水平,可能是由于灌浆条件较冷所致。Moshido Gong 502和503在两个季节都表现出较低的总生育酚含量,是研究生育酚生物合成遗传调控的良好资源。
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引用次数: 0
Loss of SYD-2 leads to decreased short-term memory in Caenorhabditis elegans. 秀丽隐杆线虫中SYD-2缺失导致短期记忆下降。
Pub Date : 2026-01-27 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.002021
Katherine Davies, Meclina Silva, Karla Vargas, Dayton Pierce

Learning and memory require tight regulation of communication between pre- and postsynaptic responses. SYD-2, the C. elegans ortholog of vertebrate liprin-α, is known for its presynaptic role in active zone maintenance but its role in learning and memory has not been previously investigated. Here, we present findings from 30-minute short-term aversive olfactory memory assay with C. elegans lacking SYD-2 ( ok217 mutants). Wild-type (N2) worms exhibited robust learning and short-term memory for aversion to diacetyl. Despite its role in presynaptic maintenance, we found that the loss of SYD-2 had no effect on aversive learning but decreased short-term associative memory.

学习和记忆需要突触前和突触后反应之间的紧密沟通。SYD-2是秀丽隐杆线虫中与脊椎动物脂素-α同源的基因,已知其在突触前活动区维持中的作用,但其在学习和记忆中的作用尚未被研究过。在这里,我们展示了对缺乏SYD-2 (ok217突变体)的秀丽隐杆线虫进行30分钟短期厌恶嗅觉记忆试验的结果。野生型(N2)蠕虫对二乙酰的厌恶表现出强大的学习和短期记忆。尽管SYD-2在突触前维持中发挥作用,但我们发现SYD-2的缺失对厌恶学习没有影响,但会降低短期联想记忆。
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引用次数: 0
Discovery of Widespread Migrasome Formation During Amoeboid Migration in Dictyostelium discoideum. 盘状盘齿龙变形虫迁移过程中广泛迁移体形成的发现。
Pub Date : 2026-01-26 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001935
Bridget K Plude, Cynthia K Damer

Migrasomes are organelles that form along retraction fibers of migrating cells and mediate intercellular communication. We performed localization studies on the calcium-dependent phospholipid-binding protein, copine E (CpnE), in Dictyostelium discoideum . We observed GFP-CpnE labeled retraction fibers and migrasomes in multiple contexts: chemotaxis toward folate, random migration, and early development. Migrasome membranes were stained with WGA and some migrasomes were stained with SYTO RNASelect, indicating the presence of RNA. Our findings suggest that CpnE may have a role in migrasome formation and indicate that migrasomes may play important roles in Dictyostelium development, cell communication, and/or homeostasis in a variety of environments.

迁移体是沿着迁移细胞的收缩纤维形成的细胞器,并介导细胞间的通讯。我们对盘状盘齿龙中钙依赖性磷脂结合蛋白copine E (CpnE)进行了定位研究。我们观察到GFP-CpnE标记的收缩纤维和迁移小体在多种情况下:趋化叶酸,随机迁移和早期发育。用WGA染色迁移小体膜,部分迁移小体用SYTO RNASelect染色,表明存在RNA。我们的研究结果表明,CpnE可能在迁移小体的形成中发挥作用,并表明迁移小体可能在各种环境下的盘基骨柱发育、细胞通讯和/或体内平衡中发挥重要作用。
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引用次数: 0
Mycobacteria isolated from temperate stony corals. 从温带石珊瑚中分离的分枝杆菌。
Pub Date : 2026-01-22 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001863
Dana Ulanova, Takuma Mezaki, Satoshi Kubota

In marine environment, actinobacteria are widely distributed in water and sediments, and form symbiotic relationships with higher organisms. In this study, we isolated 49 actinobacterial strains from three temperate stony corals , Pocillopora damicornis , Acropora hyacinthus and Acropora muricata . More than 60% of obtained actinobacterial isolates belonged to mycolic acid-containing genera, particularly members of the family Mycobacteriaceae . Our results combined with the previous studies demonstrated that these actinobacteria are frequently associated with coral hosts worldwide.

在海洋环境中,放线菌广泛分布于水体和沉积物中,并与高等生物形成共生关系。本研究从3种温带石珊瑚(Pocillopora damicornis、Acropora hyacinthus和Acropora muricata)中分离到49株放线菌。超过60%的获得的放线菌分离物属于含有霉菌酸的属,特别是分枝杆菌科的成员。我们的研究结果与之前的研究相结合,表明这些放线菌经常与世界各地的珊瑚宿主有关。
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引用次数: 0
Combat behaviors predictive of fight outcome in Gromphadorhina portentosa. 海龙战斗行为对战斗结果的预测。
Pub Date : 2026-01-22 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001927
Jim J Young, Caleb A Craven, Julianna A Koenig, Merve Addemir, Bin Z He, Olga L Miakotina, Daniel F Eberl

In the winner effect, animals that have previously won an aggressive encounter gain an increased probability of winning subsequent aggressive interactions. This effect has been studied in males of various species, from crickets to humans. However, the effects are under-studied in Madagascar hissing cockroaches, Gromphadorhina portentosa. Here, we aimed to determine the influence of the winner effect in unfavorable conflicts. To test this, smaller winner-affected male G. portentosa were placed in combat trials against substantially larger males. We tested the limits of the winner effect, and identified behaviors that were predictive to winning a match regardless of treatment group.

在赢家效应中,先前赢得攻击的动物在随后的攻击互动中获胜的可能性增加。这种效应已经在从蟋蟀到人类的各种雄性物种中进行了研究。然而,对马达加斯加嘶嘶蟑螂(Gromphadorhina portentosa)的影响还没有得到充分研究。在这里,我们的目的是确定在不利冲突中赢家效应的影响。为了验证这一点,较小的受赢家影响的雄性波顿托沙鼠被放置在与大得多的雄性的战斗试验中。我们测试了赢家效应的极限,并确定了与治疗组无关的预测赢得比赛的行为。
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引用次数: 0
Epigenetic silencing is a barrier to editing the X chromosome using the SEC-based CRISPR/Cas9 knock-in protocol in C. elegans. 在秀丽隐杆线虫中,表观遗传沉默是使用基于sec的CRISPR/Cas9敲入协议编辑X染色体的障碍。
Pub Date : 2026-01-21 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001974
Ryka Iyer, Simon Ferreria, Laahya Guvvala, Hugh Borden, Aariv Arora, Rebecca Shirsat, Ryan Doonan

Self-excising-cassette (SEC)-based CRISPR/Cas9 knock-in is widely used for generating endogenous fluorescent protein tags in C. elegans . Here, we report a lack of success targeting the X chromosome using this method. CRISPR/Cas9 works as intended, but subsequent floxing of the SEC is blocked. Given that the X chromosome is epigenetically silenced in primordial germ cells (PGCs), this is a logical result. To circumvent this barrier, we suppressed polycomb repressive complex 2 (PRC2) with RNAi to transiently and reversibly reduce silencing in the PGCs, creating a brief window where the X chromosome is amenable to floxing without compromising germ line development. Overall, our results reveal a previously unrecognized limitation of SEC-based CRISPR/Cas9 knock-in and identify a reliable workaround for tagging proteins encoded on the X chromosome.

基于SEC的CRISPR/Cas9敲入被广泛用于秀丽隐杆线虫产生内源性荧光蛋白标签。在这里,我们报告了使用这种方法靶向X染色体缺乏成功。CRISPR/Cas9按预期工作,但随后的SEC被阻止。考虑到X染色体在原始生殖细胞(PGCs)中是表观遗传沉默的,这是一个合乎逻辑的结果。为了规避这一障碍,我们用RNAi抑制多梳抑制复合体2 (PRC2),以短暂和可逆地减少PGCs中的沉默,创造一个短暂的窗口,使X染色体能够在不影响种系发育的情况下弯曲。总的来说,我们的研究结果揭示了基于sec的CRISPR/Cas9敲入的一个以前未被认识到的局限性,并确定了一个可靠的方法来标记X染色体上编码的蛋白质。
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引用次数: 0
MEP glia share molecular features with oligodendrocytes while maintaining a distinct hybrid signature. MEP胶质细胞与少突胶质细胞共享分子特征,同时保持明显的杂交特征。
Pub Date : 2026-01-21 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001970
Tessa C Dallo, Laura Fontenas

Motor Exit Point (MEP) glia are spinal cord-derived glial cells that myelinate peripheral motor axons, bridging the central and peripheral nervous systems. They have a hybrid profile, sharing features with oligodendrocytes and Schwann cells. Yet, significant gaps remain in our understanding of complex MEP glial lineage and identity. MEP glia express neural tube and canonical oligodendrocyte lineage markers olig2 and nkx2.2a , as well as the neural crest marker foxd3 . Here, we show that the oligodendrocyte markers olig1 and plp1b are not expressed in MEP glia. These findings refine the molecular signature of MEP glia, enhancing their peripheral identity.

运动出口点(MEP)胶质细胞是脊髓来源的神经胶质细胞,其髓鞘构成外周运动轴突,连接中枢和外周神经系统。它们具有杂交特征,与少突胶质细胞和雪旺细胞具有相同的特征。然而,我们对复杂的MEP神经胶质谱系和身份的理解仍然存在重大差距。MEP胶质细胞表达神经管和典型少突胶质细胞谱系标记物olig2和nkx2.2a,以及神经嵴标记物foxd3。在这里,我们发现少突胶质细胞标记物olig1和plp1b在MEP胶质细胞中不表达。这些发现完善了MEP胶质细胞的分子特征,增强了它们的外周特性。
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引用次数: 0
Efficient RFLP-based Protocol for Routine Authentication of Drosophila. 基于rflp的果蝇常规鉴定方法
Pub Date : 2026-01-21 eCollection Date: 2026-01-01 DOI: 10.17912/micropub.biology.001949
Melika Ghasemi Shiran, Nick P Bailey, Lauren McCann, Natalia Rivera-Rincón, Emma Saurette, Laurie S Stevison

Authentication of strains is important for preventing genetic contamination before any experiment, which can compromise reproducibility and lead to misleading results. Here, we developed an approach that combines computational single nucleotide polymorphism (SNP) identification with molecular validation using restriction fragment length polymorphisms (RFLPs). This workflow enables rapid and precise confirmation of strains in an inexpensive, reproducible, and easily adaptable way for long-term stock maintenance across laboratories. We apply this protocol to Drosophila melanogaster from the Drosophila Genome Resource Panel (DGRP), which are commonly used in fruit fly research, providing a reliable context for ensuring the integrity of Drosophila genetic resources.

在任何实验之前对菌株进行鉴定对于防止遗传污染非常重要,因为遗传污染会损害可重复性并导致误导性结果。在这里,我们开发了一种将计算单核苷酸多态性(SNP)鉴定与限制性片段长度多态性(RFLPs)分子验证相结合的方法。该工作流程能够以廉价,可重复且易于适应的方式快速准确地确认菌株,从而实现跨实验室的长期库存维护。我们将该方案应用于果蝇基因组资源面板(DGRP)中的黑腹果蝇(Drosophila melanogaster),该面板通常用于果蝇研究,为确保果蝇遗传资源的完整性提供了可靠的背景。
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引用次数: 0
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microPublication biology
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