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DISTRIBUTIONS OF TRIPLET CODONS IN MESSENGER RNA SECONDARY STRUCTURES 被引量:1
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作者 张静 顾宝洪 +1 位作者 彭守礼 刘次全 《Zoological Research》 CAS CSCD 1998年第5期350-358,共9页
Analysis of the secondary structures of mRNAs which encode mature peptides shows that the location of each codon in mRNA secondary structure has a trend, which appears to be in agreement with the conformational proper... Analysis of the secondary structures of mRNAs which encode mature peptides shows that the location of each codon in mRNA secondary structure has a trend, which appears to be in agreement with the conformational property of the corresponding amino acid to some extent. Most of the codons that encode hydrophobic amino acids are located in stable stem regions of mRNA secondary structures, and vice versa, most of the codons that encode hydrophilic amino acids are located in flexible loop regions. This result supports the recent conclusion that there may be the information transfer between the three dimensional structures of mRNA and the encoded protein. 展开更多
关键词 Triplet codon Amino acid mRNA secondary structure
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Evolutionary selection on synonymous codons in RNA G-quadruplex structural region
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作者 Xu Yuming Qi Ting +1 位作者 Gu Wanjun Lu Zuhong 《Journal of Southeast University(English Edition)》 EI CAS 2021年第2期177-183,共7页
To investigate how synonymous codons have been adapted to the formation of ribonucleic acid(RNA)G-quadruplex(rG4)structure,a computational searching algorithm G4Hunter was applied to detect rG4 structures in protein-c... To investigate how synonymous codons have been adapted to the formation of ribonucleic acid(RNA)G-quadruplex(rG4)structure,a computational searching algorithm G4Hunter was applied to detect rG4 structures in protein-coding sequences of mRNAs in five eukaryotic species.The native sequences forming rG4s were then compared with randomized sequences to evaluate selection on synonymous codons.Factors that may influence the formation of rG4 were also investigated,and the selection pressures of rG4 in different gene regions were compared to explore its potential roles in gene regulation.The results show universal selective pressure acts on synonymous codons in rG4 regions to facilitate rG4 formation in five eukaryotic organisms.While G-rich codon combinations are preferred in the rG4 structural region,C-rich codon combinations are selectively unfavorable for rG4 formation.Gene's codon usage bias,nucleotide composition,and evolutionary rate can account for the selective variations on synonymous codons among rG4 structures within a species.Moreover,rG4 structures in the translational initiation region showed significantly higher selective pressures than those in the translational elongation region. 展开更多
关键词 ribonucleic acid(RNA)structure G-QUADRUPLEX synonymous codons evolution SELECTION
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mRNA Dependent Virtual-Real Substitutions of Nucleotides in Codons: The Dynamics of Their Meanings in the Genome Language
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作者 P. P. Gariaev E. A. Leonova-Gariaeva 《Open Journal of Genetics》 2019年第4期77-90,共14页
This is an attempt to explain mRNA-dependent non-stationary semantic values of codons (triplets) and nucleotides (letters) in codon composition during protein biosynthesis. This explanation is realized by comparing th... This is an attempt to explain mRNA-dependent non-stationary semantic values of codons (triplets) and nucleotides (letters) in codon composition during protein biosynthesis. This explanation is realized by comparing the different protein codes of various biosystem taxa, and, comparing mitochondrial code with the standard code. An initial mRNA transcriptional virtuality (Virtual-Reality) is transformed into material reality at the level of translation of virtual triplets into real (material) amino acids or into a real stop command of protein biosynthesis. The transformation of virtuality into reality occurs de facto when the linguistic sign1 functions of the codon syhoms are realized in the 3’ nucleotide (wobbling nucleotide according to F. Crick) in the process of protein biosynthesis. This corresponds to the theoretical works of the authors of this article. Despite the illusory appearance of semantic arbitrariness during the operation of ribosomes in the mode of codon semantic non-stationarity, this phenomenon probably provides biosystems with an unusually high level of adaptability to changes in the external environment as well as to internal (mental) dynamics of neuron’s genome in the cerebral cortex. The genome’s non-stationarity properties at the nucleotide, codon, gene and mental levels have fractal structure and corresponding dimensions. The highest form of such fractality (with maximum dimension) is probably realized in the genomic continuum of neurons in the human cerebral cortex through this semantic Virtual-to-Real (VR) codon transcoding with the biosynthesis of short-living semantic proteins, as the equivalents of material thinking-consciousness. In fact, this is the language of the brain’s genome, that is, our own language. In this case, the same thing happens in natural, primarily mental (non-verbal) languages. Their materialization is recorded in vocables (sounding words) and in writing. Such writing is the amino acid sequence in the semantic proteins of the human cerebral cortex. Rapidly decaying, such proteins can leave a long-lasting “so-called” Schr&#246;dinger wave holographic memory in the cerebral cortex. The presented below study is purely theoretical and based on a logical approach. The topic of the study is very complex and is subject to further development. 展开更多
关键词 PROTEIN Biosynthesis PROTEIN Codes codons (Triplets) MRNA Virtual-Real (VR) Transcoding Semantics Thinking Consciousness
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Dependence of nucleotide physical properties on their placement in codons and determinative degree
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作者 BEREZHNOY A.Y. DUPLIJ S.A. 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2005年第10期948-960,共13页
Various physical properties such as dipole moment, heat of formation and energy of the most stable formation of nucleotides and bases were calculated by PM3 (modified neglect of diatomic overlap, parametric method num... Various physical properties such as dipole moment, heat of formation and energy of the most stable formation of nucleotides and bases were calculated by PM3 (modified neglect of diatomic overlap, parametric method number 3) and AM1 (austin model 1) methods. As distinct from previous calculations, for nucleotides the interaction with neighbours is taken into account up to gradient of convergence equaling 1. The dependencies of these variables from the place in the codon and the de- terminative degree were obtained. The difference of these variables for codons and anticodons is shown. 展开更多
关键词 DIPOLE moment Heat of formation Total energy DNA Codon Anticodon Determinative DEGREE
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Interaction of nonsense suppressor tRNAs and codon nonsense mutations or termination codons
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作者 Zixian Lu 《Advances in Biological Chemistry》 2012年第3期301-314,共14页
Codon nonsense mutations include amber, ochre, or opal mutations according to termination codon consisting of three types (TAG, TAA and TGA). Codon nonsense mutations are also divided into natural and artificial mutat... Codon nonsense mutations include amber, ochre, or opal mutations according to termination codon consisting of three types (TAG, TAA and TGA). Codon nonsense mutations are also divided into natural and artificial mutations. We discussed the interaction of codon nonsense mutations and suppressor tRNAs in vitro and in vivo. Nonsense suppressions do not only happen in prokaryotes but also in eukaryotes. Meanwhile, the misreading of termination codon and in-corporation of nonnatural amino acids into proteins are also introduced. 展开更多
关键词 NONSENSE Suppression CODON NONSENSE MUTATION SUPPRESSOR TRNAS
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Complete Genomic Sequence Analysis of Sweet Potato Virus 2 Isolates from the Shandong and Jiangsu Provinces in China
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作者 Zichen Li Jukui Ma +2 位作者 Minjun Liu Guowei Geng Hongxia Zhang 《Phyton-International Journal of Experimental Botany》 2025年第6期1841-1856,共16页
Sweet potatoes are significant cash crops,however,their yield and quality are greatly compromised by viral diseases.In this study,the complete genomic sequences of two Sweet Potato Virus 2(SPV2)isolates from infected ... Sweet potatoes are significant cash crops,however,their yield and quality are greatly compromised by viral diseases.In this study,the complete genomic sequences of two Sweet Potato Virus 2(SPV2)isolates from infected sweet potato leaves in the Shandong(designated as SPV2-SDYT,GenBank No.PQ855660.1)and Jiangsu(designated as SPV2-JSXZ,GenBank No.PQ855661.1)provinces in China were obtained using 5′RACE and RT-PCR amplification.Consistency,phylogeny,codon usage bias,recombination,and selection pressure analyses were conducted using the SPV2-SDYT and SPV2-JSXZ genome sequences.The complete genome sequences of SPV2-SDYT and SPV2-JSXZ were 10561 nucleotides(nt)in length,with respective nucleotide and amino acid identities of 99.25%and 99.12%,respectively.Both isolates were closely related to the SPV2 isolate from China(SPV2-LN).In both SPV2-SDYT and SPV2-JSXZ,the identity of the P1 protein was the highest,whereas that of the P3 protein was the lowest.There were 26 codons with relatively synonymous codon usage(RSCU)values greater than 1 in SPV2-SDYT and 27 codons with RSCU values greater than 1 in SPV2-JSXZ.High-frequency codons in their genomes were predominantly found to end with A/U.Recombination analysis revealed no major recombination sites in either SPV2-SDYT or SPV2-JSXZ.Further selection pressure analysis showed that the non-synonymous substitution rate/synonymous substitution rate(dN/dS)value of all 10 SPV2 proteins was less than 1.This is the first report on the evolutionary relationships of the 17 known SPV2 isolates.Our findings lay the molecular groundwork for preventing and controlling SPV2 infection in root-tuber crops.These findings also contribute to our understanding of the spread and evolution of SPV2,its pathogenic mechanisms,and the development of antiviral strategies against it. 展开更多
关键词 Sweet potato virus 2 consistency analysis phylogenetic analysis codon usage bias analysis recombination analysis selection pressure analysis
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The variable codons of H5N1 avian influenza A virus haemagglutinin genes
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作者 Mark J.GIBBS Robert W.MURPHY 《Science China(Life Sciences)》 SCIE CAS 2008年第11期987-993,共7页
We investigated the selection pressures on the haemagglutinin genes of H5N1 avian influenza viruses using fixed effects likelihood models. We found evidence of positive selection in the sequences from isolates from 19... We investigated the selection pressures on the haemagglutinin genes of H5N1 avian influenza viruses using fixed effects likelihood models. We found evidence of positive selection in the sequences from isolates from 1997 to 2007, except viruses from 2000. The haemagglutinin sequences of viruses from southeast Asia, Hong Kong and China's Mainland were the most polymorphic and had similar nonsyn-onymous profiles. Some sites were positively selected in viruses from most regions and a few of these sites displayed different amino acid patterns. Selection appeared to produce different outcomes in vi-ruses from Europe, Africa and Russia and from different host types. One position was found to be positively selected for human isolates only. Although the functions of some positively selected posi-tions are unknown, our analysis provided evidence of different temporal, spatial and host adaptations for H5N1 avian influenza viruses. 展开更多
关键词 positive selection pressure H5N1 AVIAN INFLUENZA virus HA CODON
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Prokaryotic expression of goldfish Tgf2 transposase with optimal codons and its enzyme activity
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作者 Xi Zhao Ruirui Si +2 位作者 Mingjuan He Xiayun Jiang Shuming Zou 《Aquaculture and Fisheries》 2019年第3期98-104,共7页
Tgf2 transposase(Tgf2-TPase),a hAT transposase from goldfish,plays an important role in fish transgenic applications.Previously,the production of the recombinant Tgf2-TPase protein required rigorous fermentation at lo... Tgf2 transposase(Tgf2-TPase),a hAT transposase from goldfish,plays an important role in fish transgenic applications.Previously,the production of the recombinant Tgf2-TPase protein required rigorous fermentation at low temperatures(22℃)and early log phase induction(OD600=0.3–0.4)in Rosetta 1(DE3)Escherichia coli lines.In order to better express the Tgf2-TPase and detect its enzyme activity,83 rare codons in Tgf2-TPase were optimized and designated Tgf2-TPase^(83).The expression results showed that the soluble recombinant Tgf2-TPase83 was highly expressed at 30℃ and was inducible at an OD600 of 0.5–0.6 in the same prokaryotic expression system.After purification by affinity chromatography,Tgf2-TPase83 with codon optimization had higher enzyme activity than the Tgf2-TPase control.Comparison of different preservation methods(freezedrying at−80℃,storage in 20%-glycerol,8%-sucrose,4%-mannitol),revealed storage of Tgf2-TPase^(83) in glycerol helped to preserve its DNase digestion activity.Furthermore,size exclusion chromatography suggested that the purified Tgf2-TPase^(83) could recognize and bind to DNA probes containing a terminal inverted repeat(TIR)and a subterminal repeat(STR)sequence of the Tgf2 transposon.Overall,the results showed that optimizing the 83 codons of Tgf2 transposase can simplify the fermentation process and improve the enzyme activity.We propose that the production of the Tgf2-Tpase83 protein in a soluble and active form could provide an alternative tool for genetic modification of fish. 展开更多
关键词 Codon optimization Enzyme activity Prokaryotic expression Tgf2 transposase
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罕见β-珠蛋白基因Codon 24(GGT>GGA)突变导致β-地中海贫血1例及文献分析
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作者 梁文雪 陈成 +2 位作者 李琦 陈萍 张学 《广西医科大学学报》 CAS 2024年第4期585-589,共5页
目的:分析罕见β-珠蛋白基因突变类型、血液学及临床特征。方法:收集疑为β-地中海贫血的病例120例。对病例进行全血细胞分类及计数、血红蛋白(Hb)电泳分析检测。用跨越断裂点PCR方法、荧光PCR熔解曲线方法、DNA测序等分析α-和β-珠蛋... 目的:分析罕见β-珠蛋白基因突变类型、血液学及临床特征。方法:收集疑为β-地中海贫血的病例120例。对病例进行全血细胞分类及计数、血红蛋白(Hb)电泳分析检测。用跨越断裂点PCR方法、荧光PCR熔解曲线方法、DNA测序等分析α-和β-珠蛋白基因突变类型。结果:120例β-地中海贫血病例中,检出1例为罕见β-珠蛋白基因突变,基因分析为Codon 24(GGT>GGA,HBB:c.75T>A)杂合子。该病例为男性,39岁,血常规检测显示:Hb 127.3 g/L,血红细胞(RBC)5.81×10^(12)/L,红细胞平均体积(MCV)70.29 fL,红细胞平均血红蛋白量(MCH)21.94 pg,红细胞平均血红蛋白浓度(MCHC)312.10 g/L。Hb分析显示Hb A_(2)4.5%,Hb F 0.4%。a-地中海贫血基因分析未发现常见的基因突变类型。结论:首次在国内发现罕见β-珠蛋白基因Codon 24(GGT>GGA,HBB:c.75T>A)突变导致β-地中海贫血。该病例在临床上易漏诊,应引起重视。 展开更多
关键词 Β-地中海贫血 Codon 24(GGT>GGA) 基因突变 临床表型
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Epidemiological Surveillance: Genetic Diversity of Rotavirus Group A in the Pearl River Delta, Guangdong, China in 2019 被引量:1
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作者 JIANG Jie Ying LIANG Dan +9 位作者 WANG Li XIAO Yun LIANG Yu Feng KE Bi Xia SU Juan XIAO Hong WANG Tao ZOU Min LI Hong Jian KE Chang Wen 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2024年第3期278-293,共16页
Objective This study aimed to understand the epidemic status and phylogenetic relationships of rotavirus group A(RVA)in the Pearl River Delta region of Guangdong Province,China.Methods This study included individuals ... Objective This study aimed to understand the epidemic status and phylogenetic relationships of rotavirus group A(RVA)in the Pearl River Delta region of Guangdong Province,China.Methods This study included individuals aged 28 days–85 years.A total of 706 stool samples from patients with acute gastroenteritis collected between January 2019 and January 2020 were analyzed for 17 causative pathogens,including RVA,using a Gastrointestinal Pathogen Panel,followed by genotyping,virus isolation,and complete sequencing to assess the genetic diversity of RVA.Results The overall RVA infection rate was 14.59%(103/706),with an irregular epidemiological pattern.The proportion of co-infection with RVA and other pathogens was 39.81%(41/103).Acute gastroenteritis is highly prevalent in young children aged 0–1 year,and RVA is the key pathogen circulating in patients 6–10 months of age with diarrhea.G9P[8](58.25%,60/103)was found to be the predominant genotype in the RVA strains,and the 41 RVA-positive strains that were successfully sequenced belonged to three different RVA genotypes in the phylogenetic analysis.Recombination analysis showed that gene reassortment events,selection pressure,codon usage bias,gene polymorphism,and post-translational modifications(PTMs)occurred in the G9P[8]and G3P[8]strains.Conclusion This study provides molecular evidence of RVA prevalence in the Pearl River Delta region of China,further enriching the existing information on its genetics and evolutionary characteristics and suggesting the emergence of genetic diversity.Strengthening the surveillance of genotypic changes and gene reassortment in RVA strains is essential for further research and a better understanding of strain variations for further vaccine development. 展开更多
关键词 Infectious diarrheal disease ROTAVIRUS Phylogenetic analysis Gene rearrangement Codon usage bias Genetic diversity
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Analysis of Codon Usage Between Different Poplar Species 被引量:9
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作者 周猛 童春发 施季森 《Journal of Genetics and Genomics》 SCIE CAS CSCD 北大核心 2007年第6期555-561,共7页
Codon usage is the selective and nonrandom use of synonymous codons to encode amino acids in genes for proteins. The analysis of codon usage may improve the understanding of cocion preferences between different specie... Codon usage is the selective and nonrandom use of synonymous codons to encode amino acids in genes for proteins. The analysis of codon usage may improve the understanding of cocion preferences between different species and allow to rebuild the codons of exogenous genes to increase the expression efficiency of exogenous genes, Here, codon DNA sequence (CDS) of four poplar species, including Populus tremuloides Michx., P. tomentosa Carr., P. deltoides Marsh., and P. trichocarpa Torr. & Gray., is used to analyze the relative frequency of synonymous codon (RFSC). High-frequency codons are selected by high-frequency (HF) codon analysis. The results indicate that the codon usage is common for all four poplar species and the codon preference is quite similar among the four poplar species. However, CCT encoding for Pro, and ACT coding for Thr are the preferred codons in P. tremuloides and P. tomentosa, whereas CCA coding for Pro, and ACA coding for Thr are preferred in P. deltoides and P. trichocarpa The codons such as TGC coding for Cys, TTC coding for Phe, and AAG coding for Lys, are preferred in the poplar species except P trichocarpa. GAG coding for Glu is preferred only in P deltoides, while the other three poplar species prefer to use GAA. The commonness of preferred codon allows exogenous gene designed by the preferred cocion of one of the different poplar species to be used in other poplar species. 展开更多
关键词 POPLAR codon usage high-frequency cocion codon preference
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p53基因codon 72多态性与乳腺癌术后放化疗疗效相关性分析 被引量:6
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作者 铁剑 解云涛 +1 位作者 徐晔 朱广迎 《中国肿瘤临床》 CAS CSCD 北大核心 2015年第3期152-156,共5页
目的:分析p53基因codon 72多态性与乳腺癌患者术后放化疗的预后相关性。方法:选取北京大学肿瘤医院乳腺癌患者术后接受放化疗427例,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析其p53基因codon 72多态性,比较不同基因... 目的:分析p53基因codon 72多态性与乳腺癌患者术后放化疗的预后相关性。方法:选取北京大学肿瘤医院乳腺癌患者术后接受放化疗427例,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析其p53基因codon 72多态性,比较不同基因型患者间复发及生存的差异。结果:全部患者基因型分布为Pro/Pro型18.3%(78/427)、Pro/Arg型44.0%(188/427)、Arg/Arg型37.7%(161/427)。3种基因型间无局部复发生存(LRFS)、无局部区域复发生存(LRRFS)、无远处转移生存(DDFS)及总生存(OS)均无显著性差异(均P〉0.05)。427例患者中雌激素受体(ER)阳性为303例,其中Arg/Arg基因型患者OS明显优于Pro/Pro基因型患者(χ2=6.330,P=0.042)。在多因素分析中p53基因codon 72多态性是ER阳性患者LRFS、LRRFS、DDFS及OS的独立预后因素,Pro/Pro基因型的患者较Arg/Arg基因型的局部复发风险增加5.9倍(HR=5.9,95%CI 1.1~31.1,P=0.036),局部区域复发风险增加3.1倍(HR=3.1,95%CI 1.1~9.1,P=0.039),远处转移风险增加2.8倍(HR=2.8,95%CI 1.3~6.0,P=0.010),死亡风险增加4倍(HR=4.0,95%CI 1.3~12.0,P=0.013)。结论:在ER阳性的乳腺癌术后接受放化疗患者中,Pro/Pro基因型的局部及局部区域复发风险、远处转移风险、死亡风险均高于Arg/Arg基因型。 展开更多
关键词 乳腺癌 放射治疗 化疗 P53基因 codon72多态性
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The Factors Shaping Synonymous Codon Usage in the Genome of Burkholderia mallei 被引量:4
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作者 赵胜 张琴 +2 位作者 陈智华 赵益新 钟金城 《Journal of Genetics and Genomics》 SCIE CAS CSCD 北大核心 2007年第4期362-372,共11页
Burkholderia mallei is regarded as a potential biological weapon by the Centers for Disease Control and Prevention. In this study, the main factors shaping codon usage in the genome of B. mallei ATCC 23344 were firstl... Burkholderia mallei is regarded as a potential biological weapon by the Centers for Disease Control and Prevention. In this study, the main factors shaping codon usage in the genome of B. mallei ATCC 23344 were firstly reported. The results showed that the primary trend in codon usage variation in the B. mallei is due to translational selection; while compositional mutation bias is relatively the weaker influence and the hydrophobicity of each protein and gene length are only the minor influences. At the same time, 21 codons defined firstly as 'optimal codons' might provide more useful information for the expression of target genes and development of a vaccine to prevent glanders. 展开更多
关键词 Burkholderia mallei ATCC 23344 codon usage correspondence analysis
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耐链霉素结核分枝杆菌rpsL基因高突变位点43Codon分子信标检测的实验研究 被引量:4
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作者 陈庆海 边志衡 +1 位作者 匡红 府伟灵 《中华医院感染学杂志》 CAS CSCD 北大核心 2008年第3期309-311,331,共4页
目的选择耐链霉素(STR)结核分枝杆菌rpsL基因主要突变位点密码子43序列设计分子信标探针及扩增体系,并建立运用荧光显微镜及图像分析软件检测荧光结果及定性判断的方法。方法运用软件Beacon designer设计43Codon分子信标探针及建立其扩... 目的选择耐链霉素(STR)结核分枝杆菌rpsL基因主要突变位点密码子43序列设计分子信标探针及扩增体系,并建立运用荧光显微镜及图像分析软件检测荧光结果及定性判断的方法。方法运用软件Beacon designer设计43Codon分子信标探针及建立其扩增体系,采用荧光显微镜观测反应后的荧光信号及图像分析软件定性判断结果。结果包含43Codon rpsL基因聚合酶链反应(PCR)扩增产物条带清晰;通过荧光显微镜观测到标准株及耐STR株PCR产物与分子信标探针杂交后荧光信号区别明显;67株耐STR与10株H37RV标准株对照组荧光信号强度比较,P<0.05和P<0.01的耐STR组检出率为80%。结论分子信标技术是一种具有高灵敏、高特异核酸检测技术;采用荧光显微镜观测荧光信号具有更强的荧光信号识别、放大功能及结果判断更准确等优点。 展开更多
关键词 耐链霉素rpsL基因 突变位点43Codon 分子信标 荧光显微镜
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p53基因codon72多态性与乳腺癌的相关性研究 被引量:2
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作者 周晓颖 张丽娜 +2 位作者 赵妍蕊 郑红 陈可欣 《中国肿瘤临床》 CAS CSCD 北大核心 2010年第9期499-503,共5页
目的:研究p53基因codon72多态性与乳腺癌患者的年龄、病理分期、淋巴结转移、雌激素受体(ER)、孕激素受体(PR)、c—erbB-2、P53蛋白表达情况的相关性。方法:TaqMan探针方法检测277例乳腺癌患者血液标本的p53基因codon72多态性。... 目的:研究p53基因codon72多态性与乳腺癌患者的年龄、病理分期、淋巴结转移、雌激素受体(ER)、孕激素受体(PR)、c—erbB-2、P53蛋白表达情况的相关性。方法:TaqMan探针方法检测277例乳腺癌患者血液标本的p53基因codon72多态性。免疫组化SP法检测匹配肿瘤纽织中ER、PR、c-erbB-2和P53蛋白的表达情况。SPSS16.0软件行统计学分析,p53基因多态性与病理学特征关系用x^2检验,非条件Logistic回归分析基因多态性与ER、PR、c—erbB-2、P53蛋白表达的相关性,计算OR值及其95%可信区间(95%CI)。P〈0.05为差异有统计学意义。结果:p53基因codon72基因型为CC/CG/GG.频率分别为22.0%、513%和26.7%,携带CC、CG、GG基因型的患者发病年龄逐渐降低,但无统计学差异;p53基因codon72多态性与临床病理学特征无关,与ER、PR、c—erbB-2和P53蛋白表达无相关性(P〉0.05)。肿瘤组织P53蛋白表达与ER、PR、c—erbB-2蛋白表达密切相关(x^2=15.492,P=0.000;x^2=3.970,P=0.046;x^2=17.956,P=0.000)。结论:p53基因codon72多态性与P55蛋白表达及病理学特征无相关性,P53蛋白表达与ER、PR、C—erbB-2蛋白表达关系密切。p53基因codon72基因型与患者发病年龄的关系有待扩大样本量进一步研究。 展开更多
关键词 P53 CODON 72 乳腺癌 免疫组化
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P53 Codon 72多态性、P53表达与宫颈癌放疗敏感性相关性的研究 被引量:2
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作者 眭鸿颖 周萍 +2 位作者 江宁 廖革望 史彩霞 《现代生物医学进展》 CAS 2011年第10期1896-1899,共4页
目的:研究P53 Codon 72多态性、P53的表达与宫颈癌放疗敏感性的相关性。方法:Ib2期宫颈癌患者274例,术前192Ir腔内后装4次,A点放疗剂量2400cGy,一周2次,共2周。治疗后14d进行广泛性子宫切除。据术后病理放疗反应HE染色结果分为放疗敏感... 目的:研究P53 Codon 72多态性、P53的表达与宫颈癌放疗敏感性的相关性。方法:Ib2期宫颈癌患者274例,术前192Ir腔内后装4次,A点放疗剂量2400cGy,一周2次,共2周。治疗后14d进行广泛性子宫切除。据术后病理放疗反应HE染色结果分为放疗敏感与放射抗拒两组。免疫组化SP法检测P53蛋白在治疗前宫颈癌组织中的表达,分析放疗敏感与放射抗拒两组P53蛋白表达差异有无显著性意义;采用PCR后测序的方法检测治疗前P53第72密码子的基因型频率多态性(P53 Codon 72),分析放疗敏感与放射抗拒两组中各P53 Codon 72基因型的差异有无显著性意义。结果:放疗抗拒组与放疗敏感组相比,P53高表达的比例显著高于P53低表达的比例(P=0.00081)。P53 Codon 72多态性分析,Pro/Pro与Arg/Arg、Pro/Pro与Arg/Pro在放疗敏感组与放疗抗拒组的分布差异显著(P值分别为P=0.009和P=0.032);Arg/Arg与Arg/Pro,在放疗敏感组与放疗抗拒组的分布无显著差异(P=0.503)。结论:P53 Codon 72多态性和P53蛋白与宫颈癌放疗敏感性有相关性,可以作为早期宫颈癌放疗敏感性的预测指标。 展开更多
关键词 P53 CODON 72多态性 P53表达 宫颈癌 放疗敏感性
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云南省住院肺癌患者HPV16/18感染及p53codon72多态性检测分析 被引量:2
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作者 周菊 游晶 +1 位作者 洪志鹏 尹小川 《中华肿瘤防治杂志》 CAS 北大核心 2015年第1期19-22,共4页
目的分析云南省住院肺癌患者HPV16/18感染以及p53codon72位点基因多态性。方法收集2012-12-01-2013-09-30昆明医科大学第一附属医院胸外科手术切除的63例肺癌组织和24例肺良性病变组织,采用聚合酶链反应(polymerase chain reaction,PCR... 目的分析云南省住院肺癌患者HPV16/18感染以及p53codon72位点基因多态性。方法收集2012-12-01-2013-09-30昆明医科大学第一附属医院胸外科手术切除的63例肺癌组织和24例肺良性病变组织,采用聚合酶链反应(polymerase chain reaction,PCR)分别检测肺癌组织和肺良性病变组织中HPV16/18以及p53codon72的DNA。结果肺癌组织的HPV16/18阳性检出率为47.63%,显著高于肺良性病变组织8.33%,χ2=11.535,P=0.001。HPV16/18感染仅与肿瘤分化程度相关,u=6.853,P=0.021;与性别(χ2=0.640,P=0.424)、年龄(χ2=0.049,P=0.825)、吸烟史(χ2=0.965,P=0.326)、肿瘤类型(u=0.593,P=0.764)、肿瘤分期(u=0.885,P=0.625)和转移情况(χ2=0.688,P=0.407)无关。p53condon72Arg/Arg、Pro/Pro和Arg/Pro在肺癌组织的分布频率分别为28.57%、53.97%和17.46%,肺良性病变组织的分布频率分别为29.17%、29.17%和41.67%,差异有统计学意义,χ2=6.489,P=0.038。p53condon72Arg/Arg、Pro/Pro和Arg/Pro在HPV阳性肺癌组织的分布频率分别为16.67%、70.00%和13.33%,在HPV阴性肺癌组织的分布频率分别为39.39%、39.39%和21.21%,差异有统计学意义,χ2=6.127,P=0.046。结论云南省住院肺癌患者中高危HPV16/18型呈高感染,p53Pro/Pro基因分型高表达,两者均为该地区肺癌发生的高危因素。 展开更多
关键词 肺肿瘤 人乳头瘤病毒 p53codon72 基因多态性 流行病学 云南
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p53 Codon 72多态性与宫颈癌关系的研究 被引量:7
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作者 郄明蓉 张燕华 吴俊梅 《华西医科大学学报》 CAS CSCD 北大核心 2002年第2期274-275,共2页
目的 探讨抑癌基因 p5 3codon72多态性与宫颈癌的关系。方法 应用聚合酶链反应法分别对15例卵巢浆液性囊腺癌、15例宫颈鳞状细胞癌和 2 0例正常妇女的 p5 3codon72多态性进行检测。结果  p5 3Arg纯合子、p5 3Pro纯合子和 p5 3Arg/ p5... 目的 探讨抑癌基因 p5 3codon72多态性与宫颈癌的关系。方法 应用聚合酶链反应法分别对15例卵巢浆液性囊腺癌、15例宫颈鳞状细胞癌和 2 0例正常妇女的 p5 3codon72多态性进行检测。结果  p5 3Arg纯合子、p5 3Pro纯合子和 p5 3Arg/ p5 3Pro杂合子在正常妇女对照组分别为 38%、6 %和 5 6 % ;而在卵巢癌组分别为 38%、5 %和 5 7% ;在宫颈癌组分别为 78%、8%和 14%。上述人群中 ,宫颈癌 p5 3Arg纯合子明显高于卵巢癌组和正常妇女对照组 (P<0 .0 5 )。结论  p5 3Arg纯合子可作为与 展开更多
关键词 p53Codon72 宫颈癌 基因多态性
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p53 codon72多态与肿瘤的相关性 被引量:7
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作者 王剑蓉 赖仁胜 《江苏医药》 CAS CSCD 北大核心 2006年第12期1138-1139,共2页
在抑癌基因中,p53与肿瘤的关系较早受到人们的重视,而且是迄今研究的最为广泛、最为系统的抗癌基因之一。p53非热点区的突变形成人群的多态性。越来越多的研究表明,位于第4外显子codon72的多态性与多种肿瘤易感性、治疗及预后存在相关... 在抑癌基因中,p53与肿瘤的关系较早受到人们的重视,而且是迄今研究的最为广泛、最为系统的抗癌基因之一。p53非热点区的突变形成人群的多态性。越来越多的研究表明,位于第4外显子codon72的多态性与多种肿瘤易感性、治疗及预后存在相关性。本文就这一方面的研究做一简要综述。并对以后p53codon72多态性的研究方向提出一些建议。 展开更多
关键词 codon72 肿瘤易感性 多态性 P53 第4外显子 抑癌基因 抗癌基因 突变形成
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p53 codon72基因多态性与宫颈癌发病风险的meta分析 被引量:3
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作者 李骏 郑全庆 《西安交通大学学报(医学版)》 CAS CSCD 北大核心 2005年第4期384-388,共5页
目的利用meta分析的方法系统评价p53 codon72多态性与宫颈癌发病风险的关系.方法检索1998~2004年Medline、Elsevier、Evidence-Based Medicine Reviews、Ovid、中国期刊网、维普科技期刊数据库等,语种不限.并追溯检索获得的已发表文献... 目的利用meta分析的方法系统评价p53 codon72多态性与宫颈癌发病风险的关系.方法检索1998~2004年Medline、Elsevier、Evidence-Based Medicine Reviews、Ovid、中国期刊网、维普科技期刊数据库等,语种不限.并追溯检索获得的已发表文献及我们研究组未发表的文献.纳入标准:涉及p53 codon72基因型频率的独立病例对照研究,各文献研究方法相似,有综合的统计指标.剔除不符合纳入标准的,重复研究报告及数据不完整的文献.用RevMan4.2软件进行统计分析.结果将总研究按病理组织学类型及种族和地域进行亚组分析,亚洲人群宫颈上皮内瘤样变(CIN)亚组和欧洲人群(主要为白种人)CIN亚组分析显示与其对照组无统计学差异.亚洲人群宫颈鳞癌(SCC)亚组合并OR=1.28,95% CI=1.05~1.55.欧洲人群SCC亚组合并OR=1.45,95% CI=1.08~1.95,P<0.01,有统计学意义.结论 p53 codon72 Arg/Arg基因型未能增加亚洲人群和欧洲人群宫颈癌前期病变发生的危险性,但与浸润性宫颈癌发病风险有正向弱相关性. 展开更多
关键词 子宫颈癌 P53基因 codon72 多态性 META分析
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