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Landscape of Sequence Variations in Homologous Copies of FAD2 and FAD3 in Rapeseed(Brassica napus L.)Germplasm with High/Low Linolenic Acid Trait
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作者 Haoxue Wu Xiaohan Zhang +5 位作者 Xiaoyu Chen Kang Li Aixia Xu Zhen Huang Jungang Dong Chengyu Yu 《Phyton-International Journal of Experimental Botany》 SCIE 2024年第3期627-640,共14页
Genetic manipulation(either restraint or enhancement)of the biosynthesis pathway ofα-linolenic acid(ALA)in seed oil is an important goal in Brassica napus breeding.B.napus is a tetraploid plant whose genome often har... Genetic manipulation(either restraint or enhancement)of the biosynthesis pathway ofα-linolenic acid(ALA)in seed oil is an important goal in Brassica napus breeding.B.napus is a tetraploid plant whose genome often har-bors four and six homologous copies,respectively,of the two fatty acid desaturases FAD2 and FAD3,which con-trol the last two steps of ALA biosynthesis during seed oil accumulation.In this study,we compared their promoters,coding sequences,and expression levels in three high-ALA inbred lines 2006L,R8Q10,and YH25005,a low-ALA line A28,a low-ALA/high-oleic-acid accession SW,and the wildtype ZS11.The expression levels of most FAD2 and FAD3 homologs in the three high-ALA accessions were higher than those in ZS11 and much higher than those in A28 and SW.The three high-ALA accessions shared similar sequences with the pro-moters and CDSs of BnFAD3.C4 and BnFAD3.A3.In A28 and SW,substitution of three amino acid residues in BnFAD2.A5 and BnFAD2.C5,an absence of BnFAD2.C1 locus,and a 549 bp long deletion on the BnFAD3.A3 promoter were detected.The profile of BnFAD2 mutation in the two low-ALA accessions A28 and SW is different from that reported in previous studies.The mutations in BnFAD3 in the high-ALA accessions are reported for thefirst time.In identifying the sites of these mutations,we provide detailed information to aid the design of mole-cular markers for accelerated breeding schemes. 展开更多
关键词 Brassica napus linolenic acid FAD2 FAD3 promoter coding sequences mutation
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Integration of Sequence Stratigraphic Analysis and 3D Geostatistical Modeling of Pliocene–Pleistocene Delta,F3 Block,Netherlands 被引量:1
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作者 Haris Ahmed KHAN Ali Asghar SHAHID +3 位作者 Muhammad Jahangir KHAN Taher ZOUAGHI Maria Dolores ALVAREZ Syed Danial Mehdi NAQVI 《Acta Geologica Sinica(English Edition)》 SCIE CAS CSCD 2023年第1期256-268,共13页
This research is focused on the analysis of the sequence stratigraphic units of F3 Block,within a wave-dominated delta of Plio–Pleistocene age.Three wells of F3 block and a 3D seismic data,are utilized in this resear... This research is focused on the analysis of the sequence stratigraphic units of F3 Block,within a wave-dominated delta of Plio–Pleistocene age.Three wells of F3 block and a 3D seismic data,are utilized in this research.The conventional techniques of 3D seismic interpretation were utilized to mark the 11 surfaces on the seismic section.Integration of seismic sequence stratigraphic interpretation,using well logs,and subsequent 3D geostatistical modeling,using seismic data,aided to evaluate the shallow hydrocarbon traps.The resulting models were obtained using System Tract and Facies models,which were generated by using sequential stimulation method and their variograms made by spherical method,moreover,these models are validated via histograms.The CDF curve generated from upscaling of well logs using geometric method,shows a good relation with less percentage of errors(1 to 2 for Facies and 3 to 4 for System Tract models)between upscaled and raw data that complements the resulted models.These approaches help us to delineate the best possible reservoir,lateral extent of system tracts(LST and/or HST)in the respective surface,and distribution of sand and shale in the delta.The clinoform break points alteration observed on seismic sections,also validates the sequence stratigraphic interpretation.The GR log-based Facies model and sequence stratigraphy-based System Tract model of SU-04-2 showed the reservoir characteristics,presence of sand bodies and majorly LST,respectively,mainly adjacent to the main fault of the studied area.Moreover,on the seismic section,SU-04-2 exhibits the presence of gas pockets at the same location that also complements the generated Facies and System Tract models.The generated models can be utilized for any similar kind of study and for the further research in the F3 block reservoir characterization. 展开更多
关键词 sequence stratigraphy facies modeling system tract modeling F3 block North Sea
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Characteristics of Seismic Sequences and Early Tendency Judgment for Yutian M_S7.3 Earthquake in 2014
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作者 Song Chunyan Zhang Linlin +2 位作者 Nie Xiaohong Xia Aiguo Wei Yunyun 《Earthquake Research in China》 CSCD 2015年第3期352-362,共11页
The basic parameters,seismogenic structure and seismic sequences characteristics of the Yutian MS7. 3 earthquake on February 12,2014 are introduced and compared to the Yutian MS7. 3 earthquake in 2008. The results sho... The basic parameters,seismogenic structure and seismic sequences characteristics of the Yutian MS7. 3 earthquake on February 12,2014 are introduced and compared to the Yutian MS7. 3 earthquake in 2008. The results show that the MS5. 4 earthquake is regarded as an immediate foreshock of the Yutian MS7. 3 main shock. The frequency of strong aftershock sequences was low and their number declined quickly,and the maximum aftershock was a MS5. 7 earthquake. According to analysis of the historical earthquake sequence type,and parameter of h-value,b-value and energy release ratio between main shock and sequence etc.,we found the preliminary conclusion that the Yutian MS7. 3 earthquake sequence in 2014 was a foreshock-main shock-aftershock type. 展开更多
关键词 Yutian Ms7. 3 earthquake Seismic sequence Strong aftershock
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基于单细胞测序数据分析养阴活胃合剂下调AQP3对MC细胞表型的影响及机制
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作者 智勇 谢姗珊 +1 位作者 邵昌明 曾斌芳 《新疆医科大学学报》 CAS 2024年第3期314-321,328,共9页
目的 观察养阴活胃合剂对MC细胞(MNNG诱导人胃黏膜上皮细胞GES-1恶性转化)增殖、迁移、侵袭及凋亡的影响,探讨其下调AQP3抑制IL-10/JAK1/STAT3信号通路激活进而阻断或逆转慢性萎缩性胃炎(CAG)病变的作用机制。方法 选取GEO数据库中的CA... 目的 观察养阴活胃合剂对MC细胞(MNNG诱导人胃黏膜上皮细胞GES-1恶性转化)增殖、迁移、侵袭及凋亡的影响,探讨其下调AQP3抑制IL-10/JAK1/STAT3信号通路激活进而阻断或逆转慢性萎缩性胃炎(CAG)病变的作用机制。方法 选取GEO数据库中的CAG单细胞转录组测序数据,绘制数据的表达矩阵。采用R语言的Seurat 4.3.0包进行处理后分群绘制UMAP可视化图谱。将MC细胞分为养阴活胃合剂组(YYHWM组)、AQP3低表达慢病毒转染组(AQP3低表达组)、养阴活胃合剂+AQP3高表达慢病毒转染组(YYHWM+AQP3高表达组)并以MC细胞和正常人胃黏膜上皮细胞GES-1分别作为模型组(MC组)和空白对照组(Control组)。采用平板克隆、划痕实验、Transwell及流式细胞术检测细胞表型变化情况,采用ELISA检测细胞培养上清IL-10表达水平,Western blot检测酪氨酸激酶1(JAK1)、信号转导和转录激活因子3(STAT3)蛋白表达水平。结果 单细胞测序数据集分析显示AQP3在CAG样本及上皮细胞群中表达升高,AQP3可能通过IL-10抗炎性信号通路影响胃癌前病变病理进程。与MC组相比,AQP3低表达组和YYHWM组细胞侵袭、迁移、增殖能力减弱,凋亡率增加,细胞培养上清中的IL-10水平降低,细胞中JAK1、STAT3蛋白表达下调(P<0.05或P<0.01),YYHWM+AQP3高表达组差异均不显著(P>0.05)。结论 养阴活胃合剂可通过下调AQP3表达抑制IL-10/JAK1/STAT3信号通路激活进而减弱MC细胞侵袭、迁移及增殖能力,促进细胞凋亡进而阻断或逆转CAG病理进程。 展开更多
关键词 养阴活胃合剂 MC细胞 细胞表型 AQP3 单细胞RNA测序
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Sin3A基因变异致Witteveen-Kolk综合征遗传学分析
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作者 卢亚亚 彭慧芳 +1 位作者 王剑 娄丹 《检验医学》 CAS 2024年第2期126-131,共6页
目的 探讨开关不敏感3转录调节因子家族成员A(Sin3A)基因变异导致的Witteveen-Kolk综合征临床表型和遗传学特点。方法 收集1例发育迟缓患儿的临床资料,对患儿及其父母进行全外显子基因测序,采用Sanger测序验证可疑变异,并进行家系分析... 目的 探讨开关不敏感3转录调节因子家族成员A(Sin3A)基因变异导致的Witteveen-Kolk综合征临床表型和遗传学特点。方法 收集1例发育迟缓患儿的临床资料,对患儿及其父母进行全外显子基因测序,采用Sanger测序验证可疑变异,并进行家系分析。结合文献分析Witteveen-Kolk综合征的临床特征和基因变异特点。结果 Witteveen-Kolk综合征患儿临床表现主要为轻中度智力障碍或发育迟缓、特殊面容(长脸、前额突出、鼻梁凹陷、长人中等)、身材矮小。颅脑磁共振成像(MRI)显示不同程度的脑畸形。全外显子基因测序结果显示,患儿Sin3A基因存在移码变异c.803dupC(p.Leu269Thrfs*37)(杂合)。Sanger测序证实存在变异位点,患儿父母该位点均为正常基因型。gnomAD等对照人群数据库未收录该变异位点,根据美国医学遗传学和基因组学学会(ACMG)/美国分子病理学学会(AMP)指南归类为“致病性”变异。结论 Sin3A基因变异可导致Witteveen-Kolk综合征。基因检测可明确生长发育迟缓伴特殊面容患儿的病因。 展开更多
关键词 开关不敏感3转录调节因子家族成员A基因 全外显子组测序 Witteveen-Kolk综合征 智力发育障碍 发育迟缓
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Catalpol Prevents Glomerular Angiogenesis Induced by Advanced Glycation End Products via Inhibiting Galectin-3 被引量:1
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作者 Wei-xiang SUN Yu-yan GAO +3 位作者 Ying CAO Jin-fu LU Gao-hong LV Hui-qin XU 《Current Medical Science》 SCIE CAS 2023年第4期668-678,共11页
Objective:The main characteristics of diabetic nephropathy(DN)at the early stage are abnormal angiogenesis of glomerular endothelial cells(GECs)and macrophage infiltration.Galectin-3 plays a pivotal role in the pathog... Objective:The main characteristics of diabetic nephropathy(DN)at the early stage are abnormal angiogenesis of glomerular endothelial cells(GECs)and macrophage infiltration.Galectin-3 plays a pivotal role in the pathogenesis of DN via binding with its ligand,advanced glycation end products(AGEs).Catalpol,an iridoid glucoside extracted from Rehmannia glutinosa,has been found to ameliorate vascular inflammation,reduce endothelial permeability,and protect against endothelial damage in diabetic milieu.However,little is known about whether catalpol could exert an anti-angiogenesis and anti-inflammation effect induced by AGEs.Methods:Mouse GECs(mGECs)and RAW 264.7 macrophages were treated with different concentrations of AGEs(0,50,100,200 and 400μg/mL)for different time(0,6,12,24 and 48 h)to determine the optimal concentration of AGEs and treatment time.Cells were treated with catalpol(10μmol/L),GB1107(1μmol/L,galectin-3 inhibitor),PX-478(50μmol/L,HIF-1αinhibitor),adenovirus-green fluorescent protein(Ad-GFP)[3×10^(7)plaque-forming unit(PFU)/mL]or Ad-galectin-3-GFP(2×10^(8)PFU/mL),which was followed by incubation with 50μg/mL AGEs.The levels of galectin-3,vascular endothelial growth factor A(VEGFA)and pro-angiogenic factors angiopoietin-1(Ang-1),angiopoietin-2(Ang-2),tunica interna endothelial cell kinase-2(Tie-2)were detected by enzyme-linked immunosorbent assay(ELISA).Cell counting kit-8(CCK-8)assay was used to evaluate the proliferation of these cells.The expression levels of galectin-3,vascular endothelial growth factor receptor 1(VEGFR1),VEGFR2,and hypoxia-inducible factor-1α(HIF-1α)in mGECs and those of galectin-3 and HIF-1αin RAW 264.7 macrophages were detected by Western blotting and immunofluorescence(IF)staining.The rat DN model was established.Catalpol(100 mg/kg)or GB1107(10 mg/kg)was administered intragastrically once a day for 12 weeks.Ad-galectin-3-GFP(6×10^(7)PFU/mL,0.5 mL)or Ad-GFP(6×10^(6)PFU/mL,0.5 mL)was injected into the tail vein of rats 48 h before the sacrifice of the animals.The expression of galectin-3,VEGFR1,.VEGFR2,and HIF-1αin renal cortices was analyzed by Western blotting.The expression of galectin-3,F4/80(a macrophage biomarker),and CD34(an endothelium biomarker)in renal cortices was detected by IF staining,and collagen accumulation by Masson staining.Results:The expression levels of galectin-3 and VEGFA were significantly higher in mGECs and RAW 264.7 macrophages treated with 50μg/mL AGEs for 48 h than those in untreated cells.Catalpol and GB1107 could block the AGEs-induced proliferation of mGECs and RAW 264.7 macrophages.Over-expression of galectin-3 was found to reduce the inhibitory effect of catalpol on the proliferation of cells.Catalpol could significantly decrease the levels of Ang-1,Ang-2 and Tie-2 released by AGEs-treated mGECs,which could be reversed by over-expression of galectin-3.Catalpol could significantly inhibit AGEs-induced expression of galectin-3,HIF-1α,VEGFR1,and VEGFR2 in mGECs.The inhibitory effect of catalpol on galectin-3 in AGEs-treated mGECs was impaired by PX-478.Moreover,catalpol attenuated the AGEs-activated HIF-1α/galectin-3 pathway in RAW 264.7 macrophages,which was weakened by PX-478.Additionally,catalpol significantly inhibited the expression of galectin-3,macrophage infiltration,collagen accumulation,and angiogenesis in the kidney of diabetic rats.Over-expression of galectin-3 could antagonize these inhibitory effects of catalpol.Conclusion:Catalpol prevented the angiogenesis of mGECs and macrophage proliferation via inhibiting galectin-3.It could prevent the progression of diabetes-induced renal damage. 展开更多
关键词 CATALPOL glomerular angiogenesis advanced glycation end products GALECTIN-3
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Use of transcriptome sequencing to explore the effect of CSRP3 on chicken myoblasts 被引量:1
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作者 SHAN Yan-ju JI Gai-ge +5 位作者 ZHANG Ming LIU Yi-fan TU Yun-jie JU Xiao-jun SHU Jing-ting ZOU Jian-min 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2023年第4期1159-1171,共13页
The mechanisms that regulate the specificity and maintenance of chicken muscle fiber types remain largely unknown. In mammals, CSRP3 has been shown to play a vital role in the maintenance of typical muscle structure a... The mechanisms that regulate the specificity and maintenance of chicken muscle fiber types remain largely unknown. In mammals, CSRP3 has been shown to play a vital role in the maintenance of typical muscle structure and function. This study investigated the role that CSRP3 plays in chicken skeletal muscle. First, the antibody against chicken CSRP3 protein was prepared, and the expression levels of the mRNA and protein of the CSRP3 gene in four chicken skeletal muscles with different myofiber compositions were compared. Then the effects of CSRP3 silencing on the expression profile of chicken myoblast transcriptomes were analyzed. The results showed that the expression levels of the mRNA and protein of the CSRP3 gene were both associated with the composition of fiber types in chicken skeletal muscles. A total of 650 genes with at least 1.5-fold differences(Q<0.05) were identified, of which 255 genes were upregulated and 395 genes were downregulated by CSRP3 silencing. Functional enrichment showed that several pathways, including adrenergic signaling in cardiomyocytes, adipocytokine signaling pathway and apelin signaling pathway, were significantly(P<0.05) enriched both in differentially expressed genes and all expressed genes. The co-expressed gene network suggested that CSRP3 silencing caused a compensatory upregulation(Q<0.05) of genes related to the assembly of myofibrils, muscle differentiation, and contraction. Meanwhile, two fast myosin heavy chain genes(MyH1B and MyH1E)were upregulated(Q<0.05) upon CSRP3 silencing. These results suggested that CSRP3 plays a crucial role in chicken myofiber composition, and affects the distribution of chicken myofiber types, probably by regulating the expression of MyH1B and MyH1E. 展开更多
关键词 CSRP3 CHICKEN myofiber type transcriptome sequencing
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绵羊肺炎支原体GH3-3株全基因组测序及生物信息学分析
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作者 田彤彤 葛家振 +4 位作者 高鹏程 李学瑞 宋国栋 郑福英 储岳峰 《生物技术通报》 CAS CSCD 北大核心 2024年第7期323-334,共12页
【目的】全面了解绵羊肺炎支原体GH3-3株的基因序列,研究其潜在的致病机制及其复制、转录、翻译过程的调控机制。【方法】采用体外培养,利用细菌基因组DNA提取试剂盒提取绵羊肺炎支原体GH3-3株基因组DNA,进行全基因组测序。【结果】绵... 【目的】全面了解绵羊肺炎支原体GH3-3株的基因序列,研究其潜在的致病机制及其复制、转录、翻译过程的调控机制。【方法】采用体外培养,利用细菌基因组DNA提取试剂盒提取绵羊肺炎支原体GH3-3株基因组DNA,进行全基因组测序。【结果】绵羊肺炎支原体GH3-3株基因组大小为1060772 bp,GC含量为29.66%,基因组组分分析后发现,GH3-3株的基因组含有730个编码基因,总长度为914379 bp,平均长度为1252.57 bp,占基因组全长的86.2%。串联重复序列共149个,总长为20926 bp,占基因组全长的1.97%。微卫星DNA序列102个,tRNA 30个,rRNA 3个。在NR、SwissProt、GOG、KEGG、GO、CARD、CAZy、PHI、TCDB、RMS数据库中,分别有719、459、473、394、449、33、5、180、113、59个基因被注释;在VFDB数据库中,共注释到了76个毒力因子相关的基因。将基因组序列提交至NCBI网站,获得登录号为:PRJNA1051969。【结论】获得了绵羊肺炎支原体GH3-3株完整的基因组信息,预测和注释了其基因的功能,明确了GH3-3株以及与国内外其他绵羊肺炎支原体菌株之间的遗传进化关系。 展开更多
关键词 绵羊肺炎支原体 GH3-3 全基因组测序 毒力因子 耐药基因
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A reduced computational load protein coding predictor using equivalent amino acid sequence of DNA string with period-3 based time and frequency domain analysis 被引量:1
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作者 Jayakishan K. Meher Gananath N. Dash +1 位作者 Pramod Kumar Meher Mukesh Kumar Raval 《American Journal of Molecular Biology》 2011年第2期79-86,共8页
Development of efficient gene prediction algorithms is one of the fundamental efforts in gene prediction study in the area of genomics. In genomic signal processing the basic step of the identification of protein codi... Development of efficient gene prediction algorithms is one of the fundamental efforts in gene prediction study in the area of genomics. In genomic signal processing the basic step of the identification of protein coding regions in DNA sequences is based on the period-3 property exhibited by nucleotides in exons. Several approaches based on signal processing tools and numerical representations have been applied to solve this problem, trying to achieve more accurate predictions. This paper presents a new indicator sequence based on amino acid sequence, called as aminoacid indicator sequence, derived from DNA string that uses the existing signal processing based time-domain and frequency domain methods to predict these regions within the billions long DNA sequence of eukaryotic cells which reduces the computational load by one-third. It is known that each triplet of bases, called as codon, instructs the cell machinery to synthesize an amino acid. The codon sequence therefore uniquely identifies an amino acid sequence which defines a protein. Thus the protein coding region is attributed by the codons in amino acid sequence. This property is used for detection of period-3 regions using amino acid sequence. Physico-chemical properties of amino acids are used for numerical representation. Various accuracy measures such as exonic peaks, discriminating factor, sensitivity, specificity, miss rate, wrong rate and approximate correlation are used to demonstrate the efficacy of the proposed predictor. The proposed method is validated on various organisms using the standard data-set HMR195, Burset and Guigo and KEGG. The simulation result shows that the proposed method is an effective approach for protein coding prediction. 展开更多
关键词 GENOMICS Bioinformatics CODON Coding region Amino Acid sequence Fourier Transform Antinotch Filter Periodicity-3 Indicator sequence
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Fidgetin interacting with microtubule end binding protein EB3 affects axonal regrowth in spinal cord injury
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作者 Chao Ma Junpei Wang +8 位作者 Qifeng Tu Weijuan Bo Zunlu Hu Run Zhuo Ronghua Wu Zhangji Dong Liang Qiang Yan Liu Mei Liu 《Neural Regeneration Research》 SCIE CAS CSCD 2023年第12期2727-2732,共6页
Fidgetin,a microtubule-severing enzyme,regulates neurite outgrowth,axonal regeneration,and cell migration by trimming off the labile domain of microtubule polymers.Because maintenance of the microtubule labile domain ... Fidgetin,a microtubule-severing enzyme,regulates neurite outgrowth,axonal regeneration,and cell migration by trimming off the labile domain of microtubule polymers.Because maintenance of the microtubule labile domain is essential for axon initiation,elongation,and navigation,it is of interest to determine whether augmenting the microtubule labile domain via depletion of fidgetin serves as a therapeutic approach to promote axonal regrowth in spinal cord injury.In this study,we constructed rat models of spinal cord injury and sciatic nerve injury.Compared with spinal cord injury,we found that expression level of tyrosinated microtubules in the labile portion of microtubules continuously increased,whereas fidgetin decreased after peripheral nerve injury.Depletion of fidgetin enhanced axon regeneration after spinal cord injury,whereas expression level of end binding protein 3(EB3)markedly increased.Next,we performed RNA interference to knockdown EB3 or fidgetin.We found that deletion of EB3 did not change fidgetin expression.Conversely,deletion of fidgetin markedly increased expression of tyrosinated microtubules and EB3.Deletion of fidgetin increased the amount of EB3 at the end of neurites and thereby increased the level of tyrosinated microtubules.Finally,we deleted EB3 and overexpressed fidgetin.We found that fidgetin trimmed tyrosinated tubulins by interacting with EB3.When fidgetin was deleted,the labile portion of microtubules was elongated,and as a result the length of axons and number of axon branches were increased.These findings suggest that fidgetin can be used as a novel therapeutic target to promote axonal regeneration after spinal cord injury.Furthermore,they reveal an innovative mechanism by which fidgetin preferentially severs labile microtubules. 展开更多
关键词 acetylated microtubules axon regeneration axonal branching axonal regrowth end binding protein 3 fidgetin microtubule dynamics sciatic nerve injury spinal cord injury tyrosinated microtubules
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Genetic Diversity of Chinese Soybean mosaic virus Strains and Their Relationships with Other Plant Potyviruses Based on P3 Gene Sequences 被引量:1
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作者 YANG Qing-hua LI Kai +1 位作者 ZHI Hai-jian GAI Jun-yi 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2014年第10期2184-2195,共12页
Soybean mosaic virus (SMV), a member of the genus Potyvirus, is a major pathogen of soybean plants in China, and 16 SMV strains have been identified nationwide based on a former detailed SMV classification system. A... Soybean mosaic virus (SMV), a member of the genus Potyvirus, is a major pathogen of soybean plants in China, and 16 SMV strains have been identified nationwide based on a former detailed SMV classification system. As the P3 gene is thought to be involved in viral replication, systemic infection, pathogenicity, and overcoming resistance, knowledge of the P3 gene sequences of SMV and other potyviruses would be useful in efforts to know the genetic relationships among them and control the disease. P3 gene sequences were obtained from representative isolates of the above-mentioned 16 SMV strains and were compared with other SMV strains and 16 Potyvirus species from the National Center for Biotechnology GenBank database. The P3 genes from the 16 SMV isolates are composed of 1041 nucleotides, encoding 347 amino acids, and share 90.7-100% nucleotide (NT) sequence identities and 95.1-100% amino acid (AA) sequence identities. The P3 coding regions of the 16 SMV isolates share high identities (92.4-98.9% NT and 96.0-100% AA) with the reported Korean isolates, followed by the USA isolates (88.5-97.9% NT and 91.4-98.6% AA), and share low identities (80.5-85.2% NT and 82.1-84.7% AA) with the reported HZ 1 and P isolates from Pinellia ternata. The sequence identities of the P3 genes between SMV and the 16 potyviruses varied from 44.4 to 81.9% in the NT sequences and from 21.4 to 85.3% in the AA sequences, respectively. Among them, SMV was closely related to Watermelon mosaic virus (WMV), with 76.0-81.9% NT and 77.5-85.3% AA identities. In addition, the SMV isolates and potyvirus species were clustered into six distinct groups. All the SMV strains isolated from soybean were clustered in Group I, and the remaining species were clustered in other groups. A multiple sequence alignment analysis of the C-terminal regions indicated that the P3 genes within a species were highly conserved, whereas those among species were relatively variable. 展开更多
关键词 Soybean mosaic virus POTYVIRUS P3 gene homology analysis phylogenetic tree multiple sequence alignment
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Subtle traps prediction using sequence stratigraphy and 3D seismic technology: A case study from Qikou depression in Huanghua basin 被引量:1
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作者 MAO Ning-bo DAI Ta-gen PENG Sheng-lin 《Journal of Central South University of Technology》 2005年第z1期141-145,共5页
Forecasting subtle traps by sequence stratigraphy and 3D seismic data is a sensitive topic in hydrocarbon exploration. Research on subtle traps by geophysical data is the most popular and difficult. Based on the suffi... Forecasting subtle traps by sequence stratigraphy and 3D seismic data is a sensitive topic in hydrocarbon exploration. Research on subtle traps by geophysical data is the most popular and difficult. Based on the sufficiently drilling data, log data, core data and 3D seismic data, sediment sequence of Qikou depression, Huanghua basin was partitioned by using sequence stratigraphy theory. Each sediment sequence system mode was built. Sediment faces of subtle traps were pointed out. Dominating factors forming subtle traps were analyzed. Sandstone seismic rock physics and its response were studied in Tertiary System. Sandstone geophysical response and elastic modulus vary laws with pressure, temperature, porosity, depth were built. Experimental result and practice shows that it is possible using seismic information forecasting subtle traps. Integrated using geology, log, drilling data, special seismic processing technique, interpretation technique, high precision horizon calibration technique, 3D seismic visualizing interpretation, seismic coherence analysis, attribute analysis, logging-constrained inversion, time frequency analysis, subtle trapsobject is identified and interpreted. Finally, advantage object of subtle trap in this area was determined. Bottomland sand stratigraphic and lithologic reservoirs in Qinan slope zone have been founded by means of high resolution 3D seismic data field technique, high resolution 3D seismic data processing technique and seismic wave impendence inversion technique. 展开更多
关键词 Huanghua BASIN sequence STRATIGRAPHY subtle TRAP SEISMIC exploration 3D SEISMIC ultrasonic wave
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血清wnt5a和LC3-Ⅱ联合MELD评分预测慢加急性乙型肝炎肝衰竭患者短期预后价值探讨
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作者 黄静 王菁 +2 位作者 方亮 周娟 商惠民 《实用肝脏病杂志》 CAS 2024年第4期551-554,共4页
目的探讨血清无翅型MMTV整合位点5a(wnt5a)和微血管相关蛋白1轻链3-Ⅱ(LC3-Ⅱ)水平联合终末期肝病模型(MELD)评分预测慢加急性乙型肝炎肝衰竭(HBV-ACLF)患者短期预后的价值。方法2018年1月~2022年12月我院诊治的152例HBV-ACLF患者,常规... 目的探讨血清无翅型MMTV整合位点5a(wnt5a)和微血管相关蛋白1轻链3-Ⅱ(LC3-Ⅱ)水平联合终末期肝病模型(MELD)评分预测慢加急性乙型肝炎肝衰竭(HBV-ACLF)患者短期预后的价值。方法2018年1月~2022年12月我院诊治的152例HBV-ACLF患者,常规内科和人工肝治疗,计算MELD评分,采用ELISA法检测血清wnt5a和LC3-Ⅱ水平,应用Logistic回归分析影响HBV-ACLF患者短期预后的因素,应用受试者工作特征(ROC)曲线评估血清wnt5a和LC3-Ⅱ联合MELD评分预测HBV-ACLF患者短期预后的效能。结果在治疗3个月内,本组HBV-ACLF患者死亡40例(26.3%);死亡组年龄、肝性脑病发生率、INR、血清总胆红素水平、MELD评分和wnt5a水平分别为(51.3±5.1)岁、70.0%、(3.2±0.9)、(441.5±89.7)μmol/L、(28.2±4.3)分和(2.8±1.5)ng/mL,均显著大于生存组【分别为(45.4±4.6)岁、20.0%、(1.7±0.3)、(280.6±73.1)μmol/L、(19.7±2.8)分和(1.3±0.2)ng/mL,P<0.05】,而外周血血小板计数和血清LC3-Ⅱ水平分别为(77.8±10.3)×10^(9)/L和(20.6±2.1)μg/mL,显著低于生存组【分别为(116.4±11.7)×10^(9)/L和(32.5±3.9)μg/mL,P<0.05】;多因素Logistic回归分析显示,年龄大、并发肝性脑病和血清wnt5a升高或血清LC3-Ⅱ水平降低为影响HBV-ACLF患者短期预后的独立影响因素(P<0.05);以MELD评分大于26.9分为截断点,其预测ACLF患者短期死亡的灵敏度和特异度分别为80.0%和92.9%,而检测血清wnt5a和LC3-Ⅱ水平也可以协助判断。结论血清wnt5a和LC3-Ⅱ联合MELD评分对HBV-ACLF患者短期预后具有较好的预测价值。 展开更多
关键词 慢加急性肝衰竭 无翅型MMTV整合位点5a 微血管相关蛋白1轻链3-Ⅱ 终末期肝病模型评分 预后 预测
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Type division and controlling factor analysis of 3rd-order sequences in marine carbonate rocks 被引量:1
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作者 Yunbo Zhang Zongju Zhao +4 位作者 Genhou Wang Zaixing Jiang Mingjian Wang Min Zheng Shiben Zhang 《Geoscience Frontiers》 SCIE CAS CSCD 2014年第2期289-298,共10页
Type division and controlling factor analysis of 3rd-order sequence are of practical significance to tec-tonic analysis, sedimentary environment identification, and other geological researches. Based on the comprehens... Type division and controlling factor analysis of 3rd-order sequence are of practical significance to tec-tonic analysis, sedimentary environment identification, and other geological researches. Based on the comprehensive analysis of carbon and oxygen isotope trends, paleobathymetry and spectral-frequency of representative well logs, 3rd-order sequences can be divided into 3 types: (a) global sea level (GSL) sequence mainly controlled by GSL change;(b) tectonic sequence mainly controlled by regional tectonic activity;and (c) composite sequence jointly controlled by GSL change and regional tectonic activity. This study aims to identify the controlling factors of 3rd-order sequences and to illustrate a new method for classification of 3rd-order sequences of the middle Permian strata in the Sichuan Basin, China. The middle Permian strata in the Sichuan Basin consist of 3 basin-contrastive 3rd-order sequences, i.e., PSQ1, PSQ2 and PSQ3. Of these, PSQ1 is a GSL sequence while PSQ2 and PSQ3 are composite sequences. The results suggest that the depositional environment was stable during the deposition of PSQ1, but was activated by tectonic activity during the deposition of the middle Permian Maokou Formation. 展开更多
关键词 Carbon isotope 3rd-Order sequence Milankovitch cycles Middle Permian strata Sichuan Basin
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TLR3基因单核苷酸多态性与儿童紫癜性肾炎的相关性
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作者 屈凤祥 常红 林毅 《精准医学杂志》 2024年第4期352-355,共4页
目的探讨TLR3基因单核苷酸多态性与儿童过敏性紫癜(Henoch-Schönlein purpura,HSP)及紫癜性肾炎(Henoch-Sch nleinöpurpura nephritis,HSPN)易感性的相关性。方法选择HSP患儿174例作为病例组,选择同期体检的162例健康儿童作... 目的探讨TLR3基因单核苷酸多态性与儿童过敏性紫癜(Henoch-Schönlein purpura,HSP)及紫癜性肾炎(Henoch-Sch nleinöpurpura nephritis,HSPN)易感性的相关性。方法选择HSP患儿174例作为病例组,选择同期体检的162例健康儿童作为对照组。根据病例组患儿在随访过程中是否合并肾脏损害分为HSP组、HSPN组。采用多重聚合酶链反应技术(M-PCR)靶向捕获TLR3基因rs35311343、rs121434431、rs199768900、rs768091235、rs1244010954位点,通过高通量测序技术对所有样本的上述位点进行测序,根据测序结果进行各位点基因型以及基因频率的统计分析。结果病例组与对照组TLR3基因rs35311343、rs121434431、rs199768900、rs768091235、rs1244010954位点的各基因型频率和各等位基因频率比较,差异无显著意义(P>0.05)。病例组中HSP组与HSPN组TLR3基因rs121434431、rs199768900、rs768091235、rs1244010954位点的各基因型频率和各等位基因频率比较,差异无显著性(P>0.05);rs35311343位点的基因型频率与等位基因频率比较差异有显著性(χ^(2)=9.492,OR=2.662,95%CI=1.342~5.281,P<0.05)。结论TLR3基因rs35311343位点CG基因型与儿童过敏性紫癜肾脏受累有关,等位基因G可能是HSPN的易感基因。 展开更多
关键词 紫癜 过敏性 TOLL样受体3 多态性 单核苷酸 肾炎 高通量核苷酸序列分析 儿童
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FUBP3 mediates the amyloid-β-induced neuronal NLRP3 expression
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作者 Jing Yao Yuan Li +5 位作者 Xi Liu Wenping Liang Yu Li Liyong Wu Zhe Wang Weihong Song 《Neural Regeneration Research》 SCIE CAS 2025年第7期2068-2083,共16页
Alzheimer's disease is characterized by deposition of amyloid-β,which forms extracellular neuritic plaques,and accumulation of hyperphosphorylated tau,which aggregates to form intraneuronal neurofibrillary tangle... Alzheimer's disease is characterized by deposition of amyloid-β,which forms extracellular neuritic plaques,and accumulation of hyperphosphorylated tau,which aggregates to form intraneuronal neurofibrillary tangles,in the brain.The NLRP3 inflammasome may play a role in the transition from amyloid-βdeposition to tau phosphorylation and aggregation.Because NLRP3 is primarily found in brain microglia,and tau is predominantly located in neurons,it has been suggested that NLRP3 expressed by microglia indirectly triggers tau phosphorylation by upregulating the expression of pro-inflammatory cytokines.Here,we found that neurons also express NLRP3 in vitro and in vivo,and that neuronal NLRP3 regulates tau phosphorylation.Using biochemical methods,we mapped the minimal NLRP3 promoter and identified FUBP3 as a transcription factor regulating NLRP3 expression in neurons.In primary neurons and the neuroblastoma cell line Neuro2A,FUBP3 is required for endogenous NLRP3 expression and tau phosphorylation only when amyloid-βis present.In the brains of aged wild-type mice and a mouse model of Alzheimer's disease,FUBP3 expression was markedly increased in cortical neurons.Transcriptome analysis suggested that FUBP3 plays a role in neuron-mediated immune responses.We also found that FUBP3 trimmed the 5′end of DNA fragments that it bound,implying that FUBP3 functions in stress-induced responses.These findings suggest that neuronal NLRP3 may be more directly involved in the amyloid-β-to–phospho-tau transition than microglial NLRP3,and that amyloid-βfundamentally alters the regulatory mechanism of NLRP3 expression in neurons.Given that FUBP3 was only expressed at low levels in young wild-type mice and was strongly upregulated in the brains of aged mice and Alzheimer's disease mice,FUBP3 could be a safe therapeutic target for preventing Alzheimer's disease progression. 展开更多
关键词 5′end trimming Alzheimer's disease AMYLOID-BETA amyloid-β-dependent transcription FUBP3 INFLAMMASOME inflammation neuron NLRP3 tau transcription factor
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干扰素调节因子3促结直肠癌细胞增殖与侵袭相关探索
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作者 徐文晖 杨畅 +3 位作者 李瑞卿 卞京 李夏伊 郑磊贞 《上海交通大学学报(医学版)》 CAS CSCD 北大核心 2024年第3期301-311,共11页
目的·分析结直肠癌中干扰素调节因子3(interferon regulatory factor 3,IRF3)表达水平与临床病理特征及患者预后的关系,观察IRF3过表达对结直肠癌细胞增殖与侵袭能力的影响及其相关蛋白通路。方法·下载癌症基因组图谱(The Can... 目的·分析结直肠癌中干扰素调节因子3(interferon regulatory factor 3,IRF3)表达水平与临床病理特征及患者预后的关系,观察IRF3过表达对结直肠癌细胞增殖与侵袭能力的影响及其相关蛋白通路。方法·下载癌症基因组图谱(The Cancer Genome Atlas,TCGA)数据,分析IRF3表达水平与恶性肿瘤患者(肾癌、结直肠癌、肝癌、前列腺癌)预后的关系。采用免疫组织化学法检测10例结直肠癌或肾癌患者的癌组织与癌旁正常组织切片中IRF3表达水平的差异。针对IRF3蛋白的C端残基位点进行改造,构建拟磷酸化IRF3-5D(396/398/402/404/405-D)高表达的HEK-293T细胞。分别在细胞培养12、24 h时,采用TANK结合激酶1(TANK-binding kinase 1,TBK1)抑制剂进行处理,并采用蛋白质印迹法检测细胞IRF3、p-IRF3(Ser386)蛋白表达水平。采用RNA测序技术探索IRF3-5D高表达与肿瘤相关蛋白表达水平的相关性。构建野生型IRF3(IRF3-WT)和IRF3-5D过表达的结直肠癌细胞CT26、COLON26,采用细胞计数法、细胞划痕试验和克隆形成试验检测细胞增殖及迁移能力。结果·TCGA数据分析提示癌组织中IRF3蛋白表达水平与患者的不良预后呈正相关。癌症患者病理组织免疫组织化学法显示,结直肠癌、肾癌组织中IRF3的表达水平显著上调,且蛋白表达集中于细胞核内。TBK1抑制剂分别在细胞培养12、24 h时间点作用后,HEK-293T细胞p-IRF3(Ser386)蛋白表达减弱。RNA测序和蛋白质印迹法结果显示,多个与癌症预后不良相关的蛋白[IRF9、细胞程序性死亡-配体1(programmed cell death 1-ligand 1,PD-L1)等]表达水平在IRF3-5D高表达的条件下显著上调。结直肠癌细胞中过表达IRF3-5D,可导致癌细胞的增殖、迁移能力显著上调。结论·结直肠癌中IRF3表达水平与患者不良预后呈正相关。IRF3-5D蛋白在结直肠癌细胞内高表达后,促进癌细胞恶性生物学行为。此外,IRF3-5D依赖于TBK1介导的IRF3活化激活通路,并上调多个肿瘤相关蛋白的表达水平。 展开更多
关键词 结直肠恶性肿瘤 靶向治疗 干扰素调节因子3 TANK结合激酶1 RNA测序
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Cloning and Sequence Analysis of cDNA Encoding MRJP3 of Apis cerana cerana
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作者 SU Song-kun ZHNEG Huo-qing +2 位作者 CHEN Sheng-lu ZHONG Bo-xiong Stefan Albert 《Agricultural Sciences in China》 CAS CSCD 2005年第9期707-713,共7页
By screening the worker (Apis cerana cerana) heads cDNA library using a fragment of the mrjp3 gene of Apis cerana as probe, 120 positive clones were obtained. The clone containing A. cerana cerana MRJP3 (AccMRJP3)... By screening the worker (Apis cerana cerana) heads cDNA library using a fragment of the mrjp3 gene of Apis cerana as probe, 120 positive clones were obtained. The clone containing A. cerana cerana MRJP3 (AccMRJP3) cDNA was selected. Based on the sequencing of the inserts of the positive clone, a sequence of AccMRJP3 cDNA which is 1 887 bp long including a poly (A) tail was obtained. The AccMRJP3 cDNA encompassed an open-reading frame (ORF) with 1 779 bp encoding 593 amino acids. The un-translated regions (UTR) of the 5′ end and 3′end are 46 bp and 160 bp in length, respectively. Similar to AmMRJP3 and AdMRJP3, the putative AccMRJP3 also has a repetitive region. The comparison of the repetitive region of AccMRJP3, AmMRJP3 and AdMRJP3 shows some differences between them. 展开更多
关键词 Apis cerana cerana MRJP3 Gene cloning sequence analysis
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LncRNA SNHG16调节miR-212-3p/FAM3C轴对食管癌细胞增殖迁移和侵袭的影响
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作者 侯英利 冯晓娜 +3 位作者 李春晖 张萌 董海平 殷星 《河北医学》 CAS 2024年第8期1238-1244,共7页
目的:探讨长链非编码小核仁RNA宿主基因16(LncRNA SNHG16)靶向微小RNA-212-3p(miR-212-3p)/序列相似家族3成员C(FAM3C)轴对食管癌细胞增殖、迁移和侵袭的影响。方法:体外培养人食管癌细胞KYSE-510作为研究对象,将其分为对照组、si-NC组... 目的:探讨长链非编码小核仁RNA宿主基因16(LncRNA SNHG16)靶向微小RNA-212-3p(miR-212-3p)/序列相似家族3成员C(FAM3C)轴对食管癌细胞增殖、迁移和侵袭的影响。方法:体外培养人食管癌细胞KYSE-510作为研究对象,将其分为对照组、si-NC组、si-SNHG16组、si-SNHG16+inhibitor NC组、si-SNHG16+miR-212-3p inhibitor组。各组细胞LncRNA SNHG16,miR-212-3p、FAM3C mRNA表达的检测用RT-qPCR法;用CCK-8试剂盒检测KYSE-510细胞增殖,用流式细胞术检测KYSE-510细胞凋亡,用划痕实验检测KYSE-510细胞迁移,用Transwell法检测KYSE-510细胞侵袭,双荧光素酶报告实验验证LncRNA SNHG16与miR-212-3p及miR-212-3p与FAM3C之间的靶向关系。结果:与对照组和si-NC组相比,si-SNHG16组中LncRNA SNHG16、FAM3C mRNA水平、OD值、划痕愈合率、细胞侵袭数降低,miR-212-3p水平、细胞凋亡率升高(P<0.05);与si-SNHG16+inhibitor NC组相比,si-SNHG16+miR-212-3p inhibitor组中miR-212-3p水平、细胞凋亡率降低、FAM3C mRNA水平、OD值、划痕愈合率、细胞侵袭数升高(P<0.05),而LncRNA SNHG16水平无差异(P>0.05);生物学信息网站预测miR-212-3p与LncRNA SNHG16和FAM3C均存在靶向结合位,且双荧光素酶报告基因实验验证了LncRNA SNHG16与miR-212-3p、miR-212-3p与FAM3C之间均存在靶向关系(P<0.05)。结论:在食管癌中LncRNA SNHG16表达上调,敲低LncRNA SNHG16的表达可靶向上调miR-212-3p,抑制FAM3C的表达,进而抑制食管癌细胞增殖、迁移和侵袭,促进食管癌细胞的凋亡。 展开更多
关键词 长链非编码小核仁RNA宿主基因16 微小RNA-212-3p/序列相似家族3成员C 食管癌 增殖 迁移 侵袭
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1例RHD-CE(3-7)-D基因重组与RHCE变异型患者的血清学与分子生物学分析
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作者 唐炳娣 蔡仲仁 +1 位作者 邓泳诗 伍昌林 《分子诊断与治疗杂志》 2024年第6期1183-1186,1190,共5页
目的 研究分析1例Rh血型弱D、弱cE患者的血清学与分子生物学特征,为该类患者的临床安全输血提供实验依据。方法 采用微柱凝胶卡法对患者红细胞进行ABO、RhDCcEe抗原的鉴定,同时采用试管法进行血型复核,抗人球蛋白卡法筛查不规则抗体;采... 目的 研究分析1例Rh血型弱D、弱cE患者的血清学与分子生物学特征,为该类患者的临床安全输血提供实验依据。方法 采用微柱凝胶卡法对患者红细胞进行ABO、RhDCcEe抗原的鉴定,同时采用试管法进行血型复核,抗人球蛋白卡法筛查不规则抗体;采用PCR-SSP法对RhDCcEe(RhD、RhC、Rhc、RhE、Rhe)基因型进行检测;三代全长测序技术对RHD/RHCE基因序列进行测序分析。结果 微柱凝胶卡法鉴定ABO、RhD、RhCcEe血型抗原的结果为:A抗原(-)、B抗原(-)、RhD(1+)、RhC(4+)、Rhc(1+)、RhE(1+)、Rhe(4+)、对照孔(-);试管法ABO、RhD、RhCcEe抗原鉴定该患者表型为:A抗原(-)、B抗原(-)、RhD(w+)、RhC(4+)、Rhc(w+)、RhE(w+)、Rhe(4+),对照管(-);抗人球蛋白卡法筛查患者不规则抗体阴性;PCR-SSP法血型基因分型RhDCcEe结果:RhD(+)、RhC(+)、Rhc(+)、RhE(+)、Rhe(+);RHD/RHCE基因结果:RHD单倍体1为外显子1-10全缺失,而单倍体2为外显子RHD-CE基因重组融合,且确认其重组类型为RHD-CE(3-7)-D,起点在外显子2(g.20238-20312之间),终点在外显子8(g49184-50480之间),同时RHCE基因第6外显子存在新碱基点突变RHCE*cE(827C>A)。结论RHD-CE(3-7)-D基因重组融合与RHCE*cE(827C>A)新等位基因突变可能引起D、cE血型抗原弱表达,为临床安全输血提供了重要的实验数据支持。 展开更多
关键词 RhD/cE弱抗原 RHD-CE(3-7)-D重组 RHCE*cE(827C>A) 三代全长测序
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