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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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Different oncological features of colorectal cancer codon-specific KRAS mutations:Not codon 13 but codon 12 have prognostic value 被引量:2
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作者 Hong-Min Ahn Duck-Woo Kim +6 位作者 Tae Gyun Lee Hye-Rim Shin In Jun Yang Jeehye Lee Jung Wook Suh Heung-Kwon Oh Sung-Bum Kang 《World Journal of Gastroenterology》 SCIE CAS 2023年第32期4883-4899,共17页
BACKGROUND Approximately 40%of colorectal cancer(CRC)cases are linked to Kirsten rat sarcoma viral oncogene homolog(KRAS)mutations.KRAS mutations are associated with poor CRC prognosis,especially KRAS codon 12 mutatio... BACKGROUND Approximately 40%of colorectal cancer(CRC)cases are linked to Kirsten rat sarcoma viral oncogene homolog(KRAS)mutations.KRAS mutations are associated with poor CRC prognosis,especially KRAS codon 12 mutation,which is associated with metastasis and poorer survival.However,the clinicopathological characteristics and prognosis of KRAS codon 13 mutation in CRC remain unclear.AIM To evaluate the clinicopathological characteristics and prognostic value of codonspecific KRAS mutations,especially in codon 13.METHODS This retrospective,single-center,observational cohort study included patients who underwent surgery for stage I-III CRC between January 2009 and December 2019.Patients with KRAS mutation status confirmed by molecular pathology reports were included.The relationships between clinicopathological characteristics and individual codon-specific KRAS mutations were analyzed.Survival data were analyzed to identify codon-specific KRAS mutations as recurrence-related factors using the Cox proportional hazards regression model.RESULTS Among the 2203 patients,the incidence of KRAS codons 12,13,and 61 mutations was 27.7%,9.1%,and 1.3%,respectively.Both KARS codons 12 and 13 mutations showed a tendency to be associated with clinical characteristics,but only codon 12 was associated with pathological features,such as stage of primary tumor(T stage),lymph node involvement(N stage),vascular invasion,perineural invasion,tumor size,and microsatellite instability.KRAS codon 13 mutation showed no associations(77.2%vs 85.3%,P=0.159),whereas codon 12 was associated with a lower 5-year recurrence-free survival rate(78.9%vs 75.5%,P=0.025).In multivariable analysis,along with T and N stages and vascular and perineural invasion,only codon 12(hazard ratio:1.399;95%confidence interval:1.034-1.894;P=0.030)among KRAS mutations was an independent risk factor for recurrence.CONCLUSION This study provides evidence that KRAS codon 13 mutation is less likely to serve as a prognostic biomarker than codon 12 mutation for CRC in a large-scale cohort. 展开更多
关键词 Genes Ras codon Colonic neoplasms Rectal neoplasms
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Genomic Landscape of Rare Codon Usage at Start Region in the Pacific Oyster Genome
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作者 SONG Kai 《Journal of Ocean University of China》 SCIE CAS CSCD 2023年第4期1041-1048,共8页
Synonymous codons have different frequencies of usage in many species.Based on the frequency of usage,the codons can be divided into two groups,rare codons and abundant codons.Rare codons are found to be enriched at t... Synonymous codons have different frequencies of usage in many species.Based on the frequency of usage,the codons can be divided into two groups,rare codons and abundant codons.Rare codons are found to be enriched at the start regions of genes,and it is assumed that these codons can reduce elongation speed of genes.However,the rare codon usage in different genomic regions of mollusks and their relationship with selective pressure has not been systematically investigated.In this study,the patterns of rare codon usage are characterized at whole genome level,and their relationship with selective pressures is investigated in Crassostrea gigas.The rare codons are enriched at the start regions of genes with high and medium expression levels,and their proportion is higher than those in the genes with low expression level.The genes with longer coding sequences and more exon numbers have lower fraction of rare codons at start regions.Rare codons have lower level of nucleotide diversity and higher frequency of rare mutations at start regions.This work is the first comprehensive investigation of the relationships between rare codon usage and some intrinsic genetic factors in mollusca species.The results suggest that the selective pressures play an important role in shaping the rare codon usage in the C.gigas genome. 展开更多
关键词 rare codons selective pressures nucleotide diversity Crassostrea gigas
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p21 codon31基因多态性与宫颈癌相关性的meta分析
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作者 刘帅妹 石慧 +6 位作者 周青 张瑞金 李孟兰 吴玉璘 封婕 黄丽丽 林宁 《中国计划生育学杂志》 2023年第6期1252-1258,共7页
目的:系统评价p21 codon31基因多态性与宫颈癌发生风险的相关性。方法:检索数据库PubMed、Web of science、Medline、中国知网、万方、维普和中国生物医学文献数据库,获取2022年8月31日之前公开发表的文章,采用5种遗传模型进行meta分析... 目的:系统评价p21 codon31基因多态性与宫颈癌发生风险的相关性。方法:检索数据库PubMed、Web of science、Medline、中国知网、万方、维普和中国生物医学文献数据库,获取2022年8月31日之前公开发表的文章,采用5种遗传模型进行meta分析,OR值和95%CI评估关联的强度。结果:共纳入19个病例对照研究,宫颈癌组3612例,对照组4135例。等位基因模型[Arg比Ser,I^(2)=80.5%,OR=1.03,95%CI0.87~1.21]、纯合比较模型[Arg/Arg比Ser/Ser,I^(2)=71.8%,OR=1.03,95%CI 0.76~1.39]、杂合比较模型[Ser/Arg比Ser/Ser,I^(2)=71.8%,OR=0.96,95%CI 0.78~1.17]、显性比较模型[(Arg/Arg+Ser/Arg)比Ser/Ser,I^(2)=83.8%,OR=0.94,95%CI 0.73~1.20]、隐性比较模型[Arg/Arg比(Ser/Ser+Ser/Arg),I^(2)=65.2%,OR=1.02,95%CI 0.80~1.30]均提示p21 codon31不会增加宫颈癌的遗传易感性。进一步对宫颈癌进行分类分析后发现,p21 codon31基因多态性与宫颈鳞癌无相关性;但纯合比较模型[Arg/Arg比Ser/Ser,I^(2)=48.4%,OR=0.53,95%CI 0.32~0.86]、显性比较模型[(Arg/Arg+Ser/Arg)比Ser/Ser,I^(2)=0.0,OR=0.61,95%CI 043~0.88]表明Arg突变型是宫颈腺癌的保护因素。结论:p21 codon31基因多态性与宫颈癌无相关性,但与宫颈腺癌有关,与宫颈鳞癌无关。 展开更多
关键词 宫颈癌 p21 codon31 基因多态性 META分析
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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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Analysis of Synonymous Codon Usage in Aeropyrum pernix K1 and Other Crenarchaeota Microorganisms 被引量:2
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作者 江澎 孙啸 陆祖宏 《Journal of Genetics and Genomics》 SCIE CAS CSCD 北大核心 2007年第3期275-284,共10页
In this study, a comparative analysis of the codon usage bias was performed in Aeropyrum pernix K1 and two other phylogenetically related Crenarchaeota microorganisms (i.e., Pyrobaculum aerophilum str. IM2 and Sulfol... In this study, a comparative analysis of the codon usage bias was performed in Aeropyrum pernix K1 and two other phylogenetically related Crenarchaeota microorganisms (i.e., Pyrobaculum aerophilum str. IM2 and Sulfolobus acidocaldarius DSM 639). The results indicated that the synonymous codon usage in A. pernix K1 was less biased, which was highly correlated with the GC3s value. The codon usage patterns were phylogenetically conserved among these Crenarchaeota microorganisms. Comparatively, it is the species function rather than the gene function that determines their gene codon usage patterns. A. pernix K1, P. aerophilum str. IM2, and S. acidocaldarius DSM 639 live in differently extreme conditions. It is presumed that the hving environment played an important role in determining the codon usage pattern of these microorganisms. Besides, there was no strain-specific codon usage among these microorganisms. The extent of codon bias in A. pernix K1 and S. acidocaldarius DSM 639 were highly correlated with the gene expression level, but no such association was detected in P. aerophilum str. IM2 genomes. 展开更多
关键词 codon usage bias relative synonymous codon usage (RSCU) Aeropyrum pernix K1
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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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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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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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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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陕西汉族人p53 codon 72基因多态性与子宫颈鳞癌易患性的关系:病例对照研究 被引量:2
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作者 李骏 郑全庆 王平 《第四军医大学学报》 CAS 北大核心 2006年第16期1499-1501,共3页
目的:探讨p5372密码基因多态性与子宫颈鳞癌易患性的关系.方法:在陕西地区汉族妇女中,对子宫颈鳞癌患者33例,健康对照51例进行病例对照研究,用聚合酶链反应法检测p53codon72多态性.结果:p53codon72Arg纯合子、pro纯合子、Arg/... 目的:探讨p5372密码基因多态性与子宫颈鳞癌易患性的关系.方法:在陕西地区汉族妇女中,对子宫颈鳞癌患者33例,健康对照51例进行病例对照研究,用聚合酶链反应法检测p53codon72多态性.结果:p53codon72Arg纯合子、pro纯合子、Arg/pro杂合子在病例组分别是33%,15%,52%;在对照组分别是22%,18%,61%.p53codon72Arg/Arg基因型与Pro/Pro和Arg/Pro两种基因型相比A值=1.80,95%CI=0.37—8.97,差异无统计意义(P〉0.05).结论:p53codon72Arg纯合子可能不增加陕西地区汉族人子宫颈鳞癌易患性. 展开更多
关键词 基因 p53 codon 72 多态现象 遗传 宫颈肿瘤 鳞状细胞
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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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Genome-wide analysis of the synonymous codon usage patterns in apple 被引量:12
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作者 LI Ning SUN Mei-hong +2 位作者 JIANG Ze-sheng SHU Huai-rui ZHANG Shi-zhong 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2016年第5期983-991,共9页
Apple(Malus×domestica) has been proposed as an important woody plant and the major cultivated fruit trees in temperate regions. Apple whole genome sequencing has been completed, which provided an excellent oppo... Apple(Malus×domestica) has been proposed as an important woody plant and the major cultivated fruit trees in temperate regions. Apple whole genome sequencing has been completed, which provided an excellent opportunity for genome-wide analysis of the synonymous codon usage patterns. In this study, a multivariate bioinformatics analysis was performed to reveal the characteristics of synonymous codon usage and the main factors affecting codon bias in apple. The neutrality, correspondence, and correlation analyses were performed by Codon W and SPSS(Statistical Product and Service Solutions) programs, indicating that the apple genome codon usage patterns were affected by mutational pressure and selective constraint. Meanwhile, coding sequence length and the hydrophobicity of proteins could also influence the codon usage patterns. In short, codon usage pattern analysis and determination of optimal codons has laid an important theoretical basis for genetic engineering, gene prediction and molecular evolution studies in apple. 展开更多
关键词 APPLE the synonymous codon usage patterns codon bias RSCU
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p53 codon72多态性在乳腺癌发生发展中的作用 被引量:2
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作者 聂伟伟 管晓翔 陈龙邦 《癌症进展》 2011年第3期295-297,270,共4页
乳腺癌仍是女性发病率和死亡率最高的肿瘤之一,约占全世界女性肿瘤的1/3。其发生率因种族和地理环境而异,其中欧美国家为高发地区,亚洲发病率则明显降低。乳腺癌发病率近年来呈明显上升趋势,但其确切的发病机制尚未阐明。
关键词 乳腺癌 p53codon72 多态性
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Synonymous codon usage in Methanosarcina mazei str.Goe1 and other Euryarchaeota microorganisms
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作者 吴昊男 笪遥 +2 位作者 魏镓伟 江澎 陆祖宏 《Journal of Southeast University(English Edition)》 EI CAS 2007年第2期289-293,共5页
A comparative analysis of the codon usage bias was conducted in Methanosarcina mazei str. Goel and two related Euryarchaeota microorganisms (Picrophilus torridus str. DSM 9790 and Natronomonas pharaonis str. DSM 2160... A comparative analysis of the codon usage bias was conducted in Methanosarcina mazei str. Goel and two related Euryarchaeota microorganisms (Picrophilus torridus str. DSM 9790 and Natronomonas pharaonis str. DSM 2160). Results revealed that synonymous codon usage in Methanosarcina mazei str. Goel was less biased, which was highly correlated with the GC3S value. And the codon usage patterns were phylogenetically conserved among those Euryarchaeota microorganisms. By employing a hierarchical clustering analysis, it can be seen that it is more the species than the gene function that determines their gene codon usage pattems. Considering that those microorganisms live in different environments where the pH conditions vary quite a lot, it can be presumed that their living environments, especially the pH conditions, play an important role in determining those microorganisms' codon usage pattems. 展开更多
关键词 codon usage bias relative synonymous codon usage (RSCU) methanosarcina mazei str. Goel
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Synonymous codon usage pattern in model legume Medicago truncatula 被引量:6
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作者 SONG Hui LIU Jing +1 位作者 CHEN Tao NAN Zhi-biao 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2018年第9期2074-2081,共8页
Synonymous codon usage pattern presumably reflects gene expression optimization as a result of molecular evolution. Though much attention has been paid to various model organisms ranging from prokaryotes to eukaryotes... Synonymous codon usage pattern presumably reflects gene expression optimization as a result of molecular evolution. Though much attention has been paid to various model organisms ranging from prokaryotes to eukaryotes, codon usage has yet been extensively investigated for model legume Medicago truncatula. In present study, 39 531 available coding sequences (CDSs) from M. truncatula were examined for codon usage bias (CUB). Based on analyses including neutrality plots, effective number of codons plots, and correlations between optimal codons frequency and codon adaptation index, we conclude that natural selection is a major driving force in M. truncatula CUB. We have identified 30 optimal codons encoding 18 amino acids based on relative synonymous codon usage. These optimal codons characteristically end with A or T, except for AGG and TTG encoding arginine and leucine respectively. Optimal codon usage is positively correlated with the GC content at three nucleotide positions of codons and the GC content of CDSs. The abundance of expressed sequence tag is a proxy for gene expression intensity in the legume, but has no relatedness with either CDS length or GC content. Collectively, we unravel the synonymous codon usage pattern in M. truncatula, which may serve as the valuable information on genetic engineering of the model legume and forage crop. 展开更多
关键词 codon usage gene expression Medicago truncatula natural selection optimal codon
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ERcodon325、PR+331G/A与乳腺癌关系的病例对照研究
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作者 靳雅丽 沈月平 +4 位作者 陈锦玲 朱岩 姚昉 张子祥 贺天锋 《肿瘤》 CAS CSCD 北大核心 2008年第10期859-863,共5页
目的:研究雌激素受体(estrogen receptor,ER)codon325、孕激素受体(progestin receptor,PR)+331G/A基因与乳腺癌的关系以及它们与环境危险因素对乳腺癌的联合作用。方法:采用病例一对照研究的方法,收集206例乳腺癌新发病例... 目的:研究雌激素受体(estrogen receptor,ER)codon325、孕激素受体(progestin receptor,PR)+331G/A基因与乳腺癌的关系以及它们与环境危险因素对乳腺癌的联合作用。方法:采用病例一对照研究的方法,收集206例乳腺癌新发病例,按年龄频数(±3岁)匹配214例健康对照女性。采用结构式调查表收集研究对象的流行病学资料,并采集3mL静脉血。应用荧光定量PCR法检测ERcodon325、PR+331G/A的基因型。结果:与CC相比,ERcodon325位点CG和GG基因型的调整OR分别为0.99(95%CI:0.61~1.61)和1.13(95%CI:0.62~2.04);与础相比,PR+331G/A位点GG基因型的调整OR为1.51(95%CI:O.74—3.07),未发现有增加乳腺癌危险的联合作用(趋势检验:P=0.4090);与无自然流产史且ERcodon325位点携带CC基因型的妇女相比,有自然流产史且携带CG和GG基因型的妇女OR为3.57(95%CI:1.21—10.52),相加模型检验接近有统计学意义(S=3.06,AP=0.97,u=1.8981,P=0.0588)。结论:ERcodon325、PR+331G/A单基因多态性可能与乳腺癌发病风险无关,ERcodon325多态性与自然流产史具有增加乳腺癌危险的联合作用趋势。 展开更多
关键词 乳腺肿瘤 多态性 单核苷酸 ER codon 325 PR+331G/A 联合作用
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