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A high-quality sponge gourd(Luffa cylindrica)genome 被引量:3
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作者 Haibin Wu Gangjun Zhao +9 位作者 Hao Gong Junxing Li Caixia Luo Xiaoli He Shaobo Luo Xiaoming Zheng Xiaoxi Liu Jinju Guo junqiu chen Jianning Luo 《Horticulture Research》 SCIE 2020年第1期1225-1234,共10页
Sponge gourd(Luffa cylindrica)is an important cultivated vegetable and medicinal plant in the family Cucurbitaceae.In this study,a draft genome sequence of the sponge gourd inbred line P93075 was analyzed.Using Illumi... Sponge gourd(Luffa cylindrica)is an important cultivated vegetable and medicinal plant in the family Cucurbitaceae.In this study,a draft genome sequence of the sponge gourd inbred line P93075 was analyzed.Using Illumina,PacBio,and 10×Genomics sequencing techniques as well as new assembly techniques such as FALCON and chromatin interaction mapping(Hi-C),a chromosome-scale genome of approximately 656.19 Mb,with an N50 scaffold length of 48.76 Mb,was generated.From this assembly,25,508 protein-coding gene loci were identified,and 63.81%of the whole-genome consisted of transposable elements,which are major contributors to the expansion of the sponge gourd genome.According to a phylogenetic analysis of conserved genes,the sponge gourd lineage diverged from the bitter gourd lineage approximately 41.6 million years ago.Additionally,many genes that respond to biotic and abiotic stresses were found to be lineage specific or expanded in the sponge gourd genome,as demonstrated by the presence of 462 NBS-LRR genes,a much greater number than are found in the genomes of other cucurbit species;these results are consistent with the high stress resistance of sponge gourd.Collectively,our study provides insights into genome evolution and serves as a valuable reference for the genetic improvement of sponge gourd. 展开更多
关键词 cylindrica SPONGE HIGH
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基于lncRNA微阵列芯片技术探索间充质干细胞外泌体增强小鼠胰岛β细胞抗低氧损伤的潜在机制
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作者 陈俊秋 邬绿莹 +3 位作者 马予洁 林娜 刘飞 陈津 《中华细胞与干细胞杂志(电子版)》 2024年第3期129-136,共8页
目的探索间充质干细胞(MSC)外泌体提高低氧条件下胰岛β细胞活性的潜在分子机制。方法将小鼠胰岛β细胞分别培养于常氧环境(5%CO_(2),95%空气)、低氧环境(2%O_(2),5%CO_(2),93%N_(2))以及低氧环境添加MSC外泌体(50μg/mL)。采用CCK-8检... 目的探索间充质干细胞(MSC)外泌体提高低氧条件下胰岛β细胞活性的潜在分子机制。方法将小鼠胰岛β细胞分别培养于常氧环境(5%CO_(2),95%空气)、低氧环境(2%O_(2),5%CO_(2),93%N_(2))以及低氧环境添加MSC外泌体(50μg/mL)。采用CCK-8检测试剂盒测定小鼠胰岛β细胞活性、细胞凋亡检测试剂盒分析小鼠胰岛β细胞凋亡情况;通过小鼠Arraystart LncRNA微阵列芯片分析不同培养环境下lncRNA和mRNA的表达情况;以Arraystart LncRNA微阵列芯片检测结果为生物信息学分析数据来源,基于t检验并设置显著性阈值P≤0.05和|Fold Change|≥2为筛选标准,筛选并获得差异表达显著的lncRNA和mRNA,采用Pearson相关系数法分析样本间lncRNA与mRNA表达情况的相关性以明确差异lncRNA的潜在靶基因,进而通过对上述靶基因进行GO和KEGG富集分析,来探究MSC外泌体通过哪条信号通路在低氧条件下增强小鼠胰岛β细胞抗低氧损伤能力。两组间数据比较采用t检验,三组间进行单因素方差分析,然后进行Dunnett's-t多重比较分析。结果CCK-8结果显示,与常氧条件相比,低氧条件下小鼠胰岛β细胞OD值(0.44±0.02比0.53±0.01)下降(t=4.455,P<0.05)。凋亡分析结果显示,与常氧培养相比,低氧条件下小鼠胰岛β细胞凋亡率(33.03%±3.12%比11.27%±2.69%)升高(t=5.289,P<0.01)。低氧培养条件下加入MSC来源外泌体干预后,小鼠胰岛β细胞活性OD值较单纯低氧培养(0.42±0.03比0.33±0.01)升高(P<0.01);小鼠胰岛β细胞凋亡率较低氧培养(15.23%±0.62%比32.63%±0.95%)降低(P<0.01)。利用LncRNA微阵列芯片完成小鼠胰岛β细胞中35293个lncRNA和24881个mRNA表达水平的检测,结果显示,与常氧培养条件相比低氧培养条件可引起1726个lncRNA和1023个mRNA表达差异;与低氧培养条件相比,加入MSC来源外泌体干预后,491个lncRNA和406个mRNA表达差异。对两种不同培养条件下差异lncRNA和mRNA利用韦恩图分别取交集,最终获得均有表达差异的lncRNA 112个、mRNA 60个;进一步相关性分析提示这112个lncRNA存在1582个潜在靶基因;进而对这些靶基因进行GO和KEGG富集分析,结果显示差异表达lncRNA靶基因主要与MAPK、自噬等信号通路等密切相关。结论低氧可引起小鼠胰岛β细胞凋亡,MSC来源外泌体可提高低氧条件下β细胞活性,抑制低氧诱发的小鼠胰岛β细胞凋亡,这可能与lncRNA调控MAPK、自噬等信号通路有关。 展开更多
关键词 胰岛Β细胞 间充质干细胞 外泌体 LncRNA
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Arabidopsis VQ10 interacts with WRKY8 to modulate basal defense against Botrytis cinerea 被引量:13
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作者 junqiu chen Houping Wang +3 位作者 Yang Li Jinjing Pan Yanru Hu Diqiu Yu 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2018年第10期956-969,共14页
Recent studies in Arabidopsis have revealed that some vq motif-containing proteins physically interact with WRKY transcription factors; however, their specific biological functions are still poorly understood. In this... Recent studies in Arabidopsis have revealed that some vq motif-containing proteins physically interact with WRKY transcription factors; however, their specific biological functions are still poorly understood. In this study, we confirmed the interaction between VQ1o and WRKY8, and show that VQ1o and WRKY8 formed a complex in the plant cell nucleus. Yeast two-hybrid analysis showed that the middle region of WRKY8 and the vq motif of vqlo are critical for their interaction, and that this interaction promotes the DNA-binding activity of WRKY8. Further investigation revealed that the VqlO protein was exclusively localized in the nucleus, and VQ1o was predominantly expressed in siliques, vQ1o expression was strongly responsive to the necrotrophic fungal pathogen, Botrytis cinerea and defense-relatedhormones. Phenotypic analysis showed that disruption of VQlo increased mutant plants susceptibility to the fungal pathogen B. cinerea, whereas constitutive-expres- sion of VQlo enhanced resistance to B. cinerea. Consis- tent with these findings, expression of the defenserelated PLANT DEFENSIN1.2 (PDFt2) gene was decreased in vqlo mutant plants, after B. cinerea infection, but increased in vQ1o-overexpressing transgenic plants. Taken together, our findings provide evidence that VQlo physically interacts with WRKY8 and positively regulates plant basal resistance against the necrotrophic fungal pathogen B. cinerea. 展开更多
关键词 Arabidopsis VQ10 interacts with WRKY8 to modulate basal defense against Botrytis cinerea VQ
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