Pub Date : 2026-02-11eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.001892
Basia Love, Jeffrey K Conner, Emily B Josephs, Sophia F Buysse
Climate change is increasing average temperature and decreasing water availability, both stressors that affect plant growth. High heat consistently decreases growth rate but plants may grow rapidly to escape drought or grow more slowly and avoid water loss. We use Arabidopsis thaliana to investigate how heat and drought together shape plant growth and if their impact differs between plants that escape or avoid drought. Our results show that leaf area growth differs but the response to heat and drought is consistent between locally adapted populations in widespread plants like A. thaliana.
{"title":"Faster vegetative growth in <i>Arabidopsis thaliana</i> in heat and drought.","authors":"Basia Love, Jeffrey K Conner, Emily B Josephs, Sophia F Buysse","doi":"10.17912/micropub.biology.001892","DOIUrl":"https://doi.org/10.17912/micropub.biology.001892","url":null,"abstract":"<p><p>Climate change is increasing average temperature and decreasing water availability, both stressors that affect plant growth. High heat consistently decreases growth rate but plants may grow rapidly to escape drought or grow more slowly and avoid water loss. We use <i>Arabidopsis thaliana</i> to investigate how heat and drought together shape plant growth and if their impact differs between plants that escape or avoid drought. Our results show that leaf area growth differs but the response to heat and drought is consistent between locally adapted populations in widespread plants like <i>A. thaliana.</i></p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12936725/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147328456","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 : 2026-02-07eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.002008
Jennifer S Lanni, Benjamin W Lyon, Stacy V Nguyen
The classic dominant longfin zebrafish strain ( lof t2 ) has long fins due to ectopic expression of the potassium channel Kcnh2a in the fin mesenchyme. Potassium channel function is also known to affect the vasculature, but the fin vasculature has not been characterized in lof t2 fish. Here we show that lof t2 fish contain significantly increased artery and vein diameters in the caudal fin as compared to wildtype fish. Interestingly, these changes in blood vessel size are associated with areas of fin overgrowth, consistent with a possible role for the vasculature in fin size regulation. .
{"title":"Increased diameter of arteries and veins in the caudal fins of <i>Danio rerio</i> <i>longfin <sup>t2</sup></i> fish is accompanied by fin overgrowth.","authors":"Jennifer S Lanni, Benjamin W Lyon, Stacy V Nguyen","doi":"10.17912/micropub.biology.002008","DOIUrl":"https://doi.org/10.17912/micropub.biology.002008","url":null,"abstract":"<p><p>The classic dominant <i>longfin</i> zebrafish strain ( <i>lof <sup>t2</sup></i> ) has long fins due to ectopic expression of the potassium channel Kcnh2a in the fin mesenchyme. Potassium channel function is also known to affect the vasculature, but the fin vasculature has not been characterized in <i>lof <sup>t2</sup> </i> fish. Here we show that <i>lof <sup>t2</sup> </i> fish contain significantly increased artery and vein diameters in the caudal fin as compared to wildtype fish. Interestingly, these changes in blood vessel size are associated with areas of fin overgrowth, consistent with a possible role for the vasculature in fin size regulation. .</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12924073/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273340","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 : 2026-02-07eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.001569
Azusa Kage, Hiroyuki J Kanaya
The ciliate protozoan Paramecium exhibits complex behaviors in response to environmental cues. Here we report a method that enables long-term observation (over 24 hours) of Paramecium with a simple experimental procedure. We observed the behavior of Paramecium bursaria , a species of Paramecium harboring symbiotic green algae, in gas-permeable chambers, where they exhibited light-dependent changes in behavior. We found that, in the 12-hour light-dark (LD) cycles, P. bursaria responds to both the dark-to-light and the light-to-dark transitions in different manners. This method provides a way to evaluate the long-term changes in the behaviors of Paramecium and other protists.
{"title":"Long-term behavioral tracking of <i>Paramecium bursaria</i>.","authors":"Azusa Kage, Hiroyuki J Kanaya","doi":"10.17912/micropub.biology.001569","DOIUrl":"https://doi.org/10.17912/micropub.biology.001569","url":null,"abstract":"<p><p>The ciliate protozoan <i>Paramecium</i> exhibits complex behaviors in response to environmental cues. Here we report a method that enables long-term observation (over 24 hours) of <i>Paramecium</i> with a simple experimental procedure. We observed the behavior of <i>Paramecium bursaria</i> , a species of <i>Paramecium</i> harboring symbiotic green algae, in gas-permeable chambers, where they exhibited light-dependent changes in behavior. We found that, in the 12-hour light-dark (LD) cycles, <i>P. bursaria</i> responds to both the dark-to-light and the light-to-dark transitions in different manners. This method provides a way to evaluate the long-term changes in the behaviors of <i>Paramecium</i> and other protists.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12924076/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273337","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 : 2026-02-06eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.001636
Abbie Wells, William H Munroe
Planaria ( Dugesia dorotocephala ) are being utilized as a model system to test the effectiveness of ARV-825. ARV-825 belongs to the drug class proteolysis targeting chimeras (PROTACs), which targets and degrades the protein Bromodomain-containing protein 4 (BRD4) via the proteasome. To examine the impact of ARV-825 on the planaria, planaria viability was tested at different ARV-825 concentrations. This demonstrated a concentration-dependent reduction in viability, 91.7% survival with 1µM ARV-825 reduced to 25% survival in 10 µM ARV-825. This suggests ARV-825 has an effect on Dugesia dorotocephala , and indicates that this may be a suitable model organism for studying ARV-825.
正利用拟涡虫(Dugesia dorotocephala)作为模型系统来测试ARV-825的有效性。ARV-825属于药物类蛋白水解靶向嵌合体(PROTACs),其通过蛋白酶体靶向并降解含有Bromodomain-containing protein 4 (BRD4)蛋白。为了研究ARV-825对涡虫的影响,研究了不同浓度ARV-825对涡虫的影响。结果表明,浓度依赖性的存活率降低,1µM ARV-825的存活率为91.7%,10µM ARV-825的存活率为25%。这表明ARV-825对多头Dugesia dorotocephala有影响,这可能是研究ARV-825的合适模式生物。
{"title":"Viability of <i>Dugesia dorotocephala</i> Planaria with the Senolytic Drug ARV-825.","authors":"Abbie Wells, William H Munroe","doi":"10.17912/micropub.biology.001636","DOIUrl":"https://doi.org/10.17912/micropub.biology.001636","url":null,"abstract":"<p><p>Planaria ( <i>Dugesia dorotocephala</i> ) are being utilized as a model system to test the effectiveness of ARV-825. ARV-825 belongs to the drug class proteolysis targeting chimeras (PROTACs), which targets and degrades the protein Bromodomain-containing protein 4 (BRD4) via the proteasome. To examine the impact of ARV-825 on the planaria, planaria viability was tested at different ARV-825 concentrations. This demonstrated a concentration-dependent reduction in viability, 91.7% survival with 1µM ARV-825 reduced to 25% survival in 10 µM ARV-825. This suggests ARV-825 has an effect on <i>Dugesia dorotocephala</i> , and indicates that this may be a suitable model organism for studying ARV-825.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12924070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273288","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 : 2026-02-06eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.002019
Geethika Burugupally, Mitsutoshi Nakamura, Cassandra Aarrestad, Susan M Parkhurst
Individual cells must rapidly repair any cortical damage from environmental or physiological stresses, to survive and to contribute to maintaining the proper function of tissues and organs. The formation of an actomyosin ring around the wound periphery is an important step in physically closing the cell wound. Here, we find that the Low-Density Lipoprotein (LDL) pathway, which is usually associated with plasma membrane homeostasis, is needed for optimal cell wound repair. In this context, the LDL pathway is required for robust actomyosin ring formation, revealing an unexpected role in regulating actin dynamics during cell wound repair.
{"title":"The LDL pathway regulates actomyosin ring dynamics necessary for optimal cell wound repair.","authors":"Geethika Burugupally, Mitsutoshi Nakamura, Cassandra Aarrestad, Susan M Parkhurst","doi":"10.17912/micropub.biology.002019","DOIUrl":"https://doi.org/10.17912/micropub.biology.002019","url":null,"abstract":"<p><p>Individual cells must rapidly repair any cortical damage from environmental or physiological stresses, to survive and to contribute to maintaining the proper function of tissues and organs. The formation of an actomyosin ring around the wound periphery is an important step in physically closing the cell wound. Here, we find that the Low-Density Lipoprotein (LDL) pathway, which is usually associated with plasma membrane homeostasis, is needed for optimal cell wound repair. In this context, the LDL pathway is required for robust actomyosin ring formation, revealing an unexpected role in regulating actin dynamics during cell wound repair.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12924074/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273320","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 : 2026-02-05eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.002026
Michael Zoberman, John A Calarco
The C. eleganssmg-1 gene encodes a PI3K-related kinase responsible for initiating the process of nonsense-mediated decay (NMD). The smg-1 ( r861 ) allele is a strong loss-of-function variant that disrupts NMD activity leading to the stabilization of transcripts containing premature stop codons (PTCs). This allele has been used extensively in studies of RNA surveillance, transcript stability, and transgene regulation. Despite its widespread use, the mutation in smg-1 ( r861 ) has not been reported, and identification is often based solely on phenotype. Here, we identify the underlying mutation and present a restriction digestion-based genotyping strategy that enables quick confirmation of the smg-1 ( r861 ) allele.
{"title":"Variant identification and genotyping strategy for the <i>smg-1(r861)</i> allele in <i>Caenorhabditis elegans</i>.","authors":"Michael Zoberman, John A Calarco","doi":"10.17912/micropub.biology.002026","DOIUrl":"https://doi.org/10.17912/micropub.biology.002026","url":null,"abstract":"<p><p>The <i>C. elegans</i> <i>smg-1</i> gene encodes a PI3K-related kinase responsible for initiating the process of nonsense-mediated decay (NMD). The <i>smg-1 ( r861 )</i> allele is a strong loss-of-function variant that disrupts NMD activity leading to the stabilization of transcripts containing premature stop codons (PTCs). This allele has been used extensively in studies of RNA surveillance, transcript stability, and transgene regulation. Despite its widespread use, the mutation in <i>smg-1 ( r861 )</i> has not been reported, and identification is often based solely on phenotype. Here, we identify the underlying mutation and present a restriction digestion-based genotyping strategy that enables quick confirmation of the <i>smg-1 ( r861 )</i> allele.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12921447/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273293","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}
The promoter of the ArabidopsisMYB93 ( MYB93 ) transcription factor was previously identified in a large-scale screen using the SCARECROW ( SCR ) transcription factor. Independent high-throughput studies also identified MYB93 as a protein-interaction partner of the MAP kinase 3 ( MPK3 ). Here, we validate and extend those observations using RT-PCR, yeast two-hybrid assays and phenotypic analysis. MYB93 transcript levels were elevated in the scr-3 mutant and reduced upon expression of SCR-GFP, indicating regulation by SCR. In yeast, the N-terminal domain of MYB93 , but not the C-terminal region, interacted with MPK3 . We also observed that mpk3-1 mutants exhibited a lateral root phenotype similar to myb93-1 . Together, these findings support a model in which both MYB93 gene expression and MYB93 protein function are modulated by SCR and MPK3 , respectively.
{"title":"Possible regulation of <i>Arabidopsis</i> MYB93 by both SCARECROW and MPK3.","authors":"Xulyu Cao, Clare Clayton, Bethany Hutton, Nancy McMulkin, Juliet C Coates","doi":"10.17912/micropub.biology.001986","DOIUrl":"https://doi.org/10.17912/micropub.biology.001986","url":null,"abstract":"<p><p>The promoter of the <i>Arabidopsis</i> <i>MYB93</i> ( <i>MYB93</i> ) transcription factor was previously identified in a large-scale screen using the SCARECROW ( SCR ) transcription factor. Independent high-throughput studies also identified MYB93 as a protein-interaction partner of the MAP kinase 3 ( MPK3 ). Here, we validate and extend those observations using RT-PCR, yeast two-hybrid assays and phenotypic analysis. <i>MYB93</i> transcript levels were elevated in the <i>scr-3</i> mutant and reduced upon expression of SCR-GFP, indicating regulation by SCR. In yeast, the N-terminal domain of MYB93 , but not the C-terminal region, interacted with MPK3 . We also observed that <i>mpk3-1</i> mutants exhibited a lateral root phenotype similar to <i>myb93-1</i> . Together, these findings support a model in which both <i>MYB93</i> gene expression and MYB93 protein function are modulated by SCR and MPK3 , respectively.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12921443/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273305","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 : 2026-02-03eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.001768
JoonJae Kim, Lucia Strader, Suresh Damodaran
Grafting and adventitious root formation are plant regeneration mechanisms used in horticulture. In grafting, a scion (shoot) of one plant is joined to a stock (root) of another plant through vascular reconnection. Adventitious roots arise from above-ground plant tissue, and graft failure occurs when the scion develops adventitious roots. The molecular mechanisms underlying grafting success and adventitious root formation are unclear. We developed a hypocotyl grafting approach to determine regulators involved in grafting success vs adventitious root formation. We suggest that reduced cytokinin signaling by the F-box protein, KISS ME DEADLY2 (KMD2, AT1G15670), promotes adventitious root formation over successful grafting. .
嫁接和不定根形成是园艺中常用的植物再生机制。在嫁接中,一株植物的接穗(茎)通过维管重连与另一株植物的砧木(根)相连。不定根产生于地上植物组织,接穗发育不定根时发生嫁接失败。嫁接成功和不定根形成的分子机制尚不清楚。我们开发了一种下胚轴嫁接方法来确定嫁接成功与不定根形成相关的调节因子。我们认为,F-box蛋白KISS ME DEADLY2 (KMD2, AT1G15670)的细胞分裂素信号传导减少,促进了嫁接成功后不定根的形成。
{"title":"Cytokinin signaling mediated by KMD2 promotes Arabidopsis hypocotyl grafting success.","authors":"JoonJae Kim, Lucia Strader, Suresh Damodaran","doi":"10.17912/micropub.biology.001768","DOIUrl":"https://doi.org/10.17912/micropub.biology.001768","url":null,"abstract":"<p><p>Grafting and adventitious root formation are plant regeneration mechanisms used in horticulture. In grafting, a scion (shoot) of one plant is joined to a stock (root) of another plant through vascular reconnection. Adventitious roots arise from above-ground plant tissue, and graft failure occurs when the scion develops adventitious roots. The molecular mechanisms underlying grafting success and adventitious root formation are unclear. We developed a hypocotyl grafting approach to determine regulators involved in grafting success <i>vs</i> adventitious root formation. We suggest that reduced cytokinin signaling by the F-box protein, KISS ME DEADLY2 (KMD2, AT1G15670), promotes adventitious root formation over successful grafting. .</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12910299/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146222457","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 : 2026-02-03eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.001972
Brett E Harris, Helena E Heiberger, ByungHoon B Kim
Plant shade avoidance response includes elongated hypocotyls and petioles as well as increased leaf elevation angles. Our time-course image analyses indicate that the phytohormone abscisic acid (ABA) affects leaf elevation angles in Arabidopsis. While mutants with impaired ABA production ( aba1-6 ) or with insensitivity to ABA ( abi5-10 ) did not fully increase the angles under shade avoidance conditions, a higher concentration of exogenous ABA inhibited leaf elevation under the same conditions. These suggest that certain levels of ABA production and sensing are required for leaf elevation during shade avoidance response, whereas higher concentrations of ABA can inhibit the process.
{"title":"Exogenous abscisic acid inhibits leaf elevation during shade avoidance response in <i>Arabidopsis thaliana</i>.","authors":"Brett E Harris, Helena E Heiberger, ByungHoon B Kim","doi":"10.17912/micropub.biology.001972","DOIUrl":"https://doi.org/10.17912/micropub.biology.001972","url":null,"abstract":"<p><p>Plant shade avoidance response includes elongated hypocotyls and petioles as well as increased leaf elevation angles. Our time-course image analyses indicate that the phytohormone abscisic acid (ABA) affects leaf elevation angles in Arabidopsis. While mutants with impaired ABA production ( <i>aba1-6</i> ) or with insensitivity to ABA ( <i>abi5-10</i> ) did not fully increase the angles under shade avoidance conditions, a higher concentration of exogenous ABA inhibited leaf elevation under the same conditions. These suggest that certain levels of ABA production and sensing are required for leaf elevation during shade avoidance response, whereas higher concentrations of ABA can inhibit the process.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12910301/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146222412","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 : 2026-02-03eCollection Date: 2026-01-01DOI: 10.17912/micropub.biology.001936
Ombeline Rossier, Florence Constantinesco-Becker, Anne Lopes, Daniel Delaruelle, Ana A Arteni, Lydia Hassissene, Malika Ouldali, Laura Pieri, Avril Zappini, Katia Zaidi, Armand Tomasella, Perla Tannous, Michel Nouhra, Mickael Marques, Cindy Goodur, Louis Gachot, Erine Dumond, Alizée Dias, Heather Desolle, Meissan Chikhi, Chahine Belhachem, Adel Amriche, Christophe Regeard
MicyPS is a bacteriophage with siphovirus morphology infecting Corynebacterium glutamicum strain MB001. It was isolated from soil near a henhouse in Villiers-sur-Marne, France. Its 78,208-bp genome encodes 115 predicted protein-encoding genes and 5 tRNAs. Based on gene-content similarity with actinobacteriophage PSonyx, MicyPS was assigned to the new cluster EQ.
{"title":"Genome Sequence of <i>Corynebacterium glutamicum</i> Phage MicyPS.","authors":"Ombeline Rossier, Florence Constantinesco-Becker, Anne Lopes, Daniel Delaruelle, Ana A Arteni, Lydia Hassissene, Malika Ouldali, Laura Pieri, Avril Zappini, Katia Zaidi, Armand Tomasella, Perla Tannous, Michel Nouhra, Mickael Marques, Cindy Goodur, Louis Gachot, Erine Dumond, Alizée Dias, Heather Desolle, Meissan Chikhi, Chahine Belhachem, Adel Amriche, Christophe Regeard","doi":"10.17912/micropub.biology.001936","DOIUrl":"https://doi.org/10.17912/micropub.biology.001936","url":null,"abstract":"<p><p>MicyPS is a bacteriophage with siphovirus morphology infecting <i>Corynebacterium glutamicum</i> strain MB001. It was isolated from soil near a henhouse in Villiers-sur-Marne, France. Its 78,208-bp genome encodes 115 predicted protein-encoding genes and 5 tRNAs. Based on gene-content similarity with actinobacteriophage PSonyx, MicyPS was assigned to the new cluster EQ.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12921444/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147273346","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}