Pub Date : 2026-02-02eCollection Date: 2026-01-01DOI: 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.
{"title":"Expression of the <i>siss-1</i> gene in <i>C. elegans</i>.","authors":"Marine Barsegyan, Cheryl Van Buskirk","doi":"10.17912/micropub.biology.001976","DOIUrl":"https://doi.org/10.17912/micropub.biology.001976","url":null,"abstract":"<p><p><i>C. elegans</i> 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 <i>siss-1</i> should be widely expressed. Here we investigate <i>siss-1</i> expression using both endogenous and transgenic fluorescent reporters. Our endogenous reporter reveals <i>siss-1</i> 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.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12910300/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146222448","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-02eCollection Date: 2026-01-01DOI: 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.
{"title":"Assay of Ds2 Transposition Activity in the Maize W22.","authors":"Harpreet Kaur, Matthew Bacchus, Lilly Horowitz, Caroline Larow, Vedant Rawat, Dafang Wang","doi":"10.17912/micropub.biology.001902","DOIUrl":"https://doi.org/10.17912/micropub.biology.001902","url":null,"abstract":"<p><p><i>Ds</i> elements are non-autonomous DNA transposons requiring <i>Ac</i> transposase for mobility. From the 39 <i>Ds2</i> elements reported in B73, we identified 38 <i>Ds2</i> 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 <i>Ds2-23</i> showed suggestive somatic transposition. Targeted bisulfite sequencing revealed that while <i>Ac</i> 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 <i>Ds2</i> transposition variation in W22.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12910297/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146222376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-27eCollection Date: 2026-01-01DOI: 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。
{"title":"Tocopherol Profile Variations of Soybean World Mini-Core Collection Accessions Grown in Hokkaido.","authors":"Maria Stefanie Dwiyanti","doi":"10.17912/micropub.biology.001813","DOIUrl":"10.17912/micropub.biology.001813","url":null,"abstract":"<p><p>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. <i>Moshido Gong 502</i> and <i>503</i> showed low total tocopherol content in both seasons, making them promising resources for investigating genetic regulation of tocopherol biosynthesis.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12892100/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146183650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-27eCollection Date: 2026-01-01DOI: 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.
{"title":"Loss of SYD-2 leads to decreased short-term memory in <i>Caenorhabditis elegans</i>.","authors":"Katherine Davies, Meclina Silva, Karla Vargas, Dayton Pierce","doi":"10.17912/micropub.biology.002021","DOIUrl":"10.17912/micropub.biology.002021","url":null,"abstract":"<p><p>Learning and memory require tight regulation of communication between pre- and postsynaptic responses. SYD-2, the <i>C. elegans</i> 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 <i>C. elegans</i> lacking SYD-2 ( <i>ok217</i> 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.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12887595/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146168239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-26eCollection Date: 2026-01-01DOI: 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。
{"title":"Discovery of Widespread Migrasome Formation During Amoeboid Migration in <i>Dictyostelium discoideum</i>.","authors":"Bridget K Plude, Cynthia K Damer","doi":"10.17912/micropub.biology.001935","DOIUrl":"10.17912/micropub.biology.001935","url":null,"abstract":"<p><p>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 <i>Dictyostelium discoideum</i> . 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 <i>Dictyostelium</i> development, cell communication, and/or homeostasis in a variety of environments.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12887596/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146168197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-22eCollection Date: 2026-01-01DOI: 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.
{"title":"Mycobacteria isolated from temperate stony corals.","authors":"Dana Ulanova, Takuma Mezaki, Satoshi Kubota","doi":"10.17912/micropub.biology.001863","DOIUrl":"10.17912/micropub.biology.001863","url":null,"abstract":"<p><p>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 <i>, Pocillopora damicornis</i> , <i>Acropora hyacinthus</i> and <i>Acropora muricata</i> . More than 60% of obtained actinobacterial isolates belonged to mycolic acid-containing genera, particularly members of the family <i>Mycobacteriaceae</i> . Our results combined with the previous studies demonstrated that these actinobacteria are frequently associated with coral hosts worldwide.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12877790/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146145074","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-22eCollection Date: 2026-01-01DOI: 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.
{"title":"Combat behaviors predictive of fight outcome in <i>Gromphadorhina portentosa</i>.","authors":"Jim J Young, Caleb A Craven, Julianna A Koenig, Merve Addemir, Bin Z He, Olga L Miakotina, Daniel F Eberl","doi":"10.17912/micropub.biology.001927","DOIUrl":"10.17912/micropub.biology.001927","url":null,"abstract":"<p><p>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, <i>Gromphadorhina portentosa.</i> Here, we aimed to determine the influence of the winner effect in unfavorable conflicts. To test this, smaller winner-affected male <i>G. portentosa</i> 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.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12877791/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146145050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21eCollection Date: 2026-01-01DOI: 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.
{"title":"Epigenetic silencing is a barrier to editing the X chromosome using the SEC-based CRISPR/Cas9 knock-in protocol in <i>C. elegans</i>.","authors":"Ryka Iyer, Simon Ferreria, Laahya Guvvala, Hugh Borden, Aariv Arora, Rebecca Shirsat, Ryan Doonan","doi":"10.17912/micropub.biology.001974","DOIUrl":"10.17912/micropub.biology.001974","url":null,"abstract":"<p><p>Self-excising-cassette (SEC)-based CRISPR/Cas9 knock-in is widely used for generating endogenous fluorescent protein tags in <i>C. elegans</i> . 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.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12873579/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146145004","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21eCollection Date: 2026-01-01DOI: 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.
{"title":"MEP glia share molecular features with oligodendrocytes while maintaining a distinct hybrid signature.","authors":"Tessa C Dallo, Laura Fontenas","doi":"10.17912/micropub.biology.001970","DOIUrl":"10.17912/micropub.biology.001970","url":null,"abstract":"<p><p>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 <i>olig2</i> and <i>nkx2.2a</i> , as well as the neural crest marker <i>foxd3</i> . Here, we show that the oligodendrocyte markers <i>olig1</i> and <i>plp1b</i> are not expressed in MEP glia. These findings refine the molecular signature of MEP glia, enhancing their peripheral identity.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12873578/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21eCollection Date: 2026-01-01DOI: 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.
{"title":"Efficient RFLP-based Protocol for Routine Authentication of Drosophila.","authors":"Melika Ghasemi Shiran, Nick P Bailey, Lauren McCann, Natalia Rivera-Rincón, Emma Saurette, Laurie S Stevison","doi":"10.17912/micropub.biology.001949","DOIUrl":"10.17912/micropub.biology.001949","url":null,"abstract":"<p><p>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 <i>Drosophila melanogaster</i> 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.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12873577/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146145046","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}