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定点诱变

定点诱变的相关文献在1989年到2022年内共计98篇,主要集中在分子生物学、生物化学、生物工程学(生物技术) 等领域,其中期刊论文86篇、会议论文3篇、专利文献8029篇;相关期刊56种,包括生命科学研究、生物化学与生物物理进展、生物化学与生物物理学报:英文版等; 相关会议3种,包括福建省科协第十四届学术年会农业分会暨华东地区农学会学术年会、第三届全国细菌耐药监测与临床专题学术会议、中国检验医学中青年论坛等;定点诱变的相关文献由332位作者贡献,包括刘平、A.亨里克森、C.维贝里等。

定点诱变—发文量

期刊论文>

论文:86 占比:1.06%

会议论文>

论文:3 占比:0.04%

专利文献>

论文:8029 占比:98.90%

总计:8118篇

定点诱变—发文趋势图

定点诱变

-研究学者

  • 刘平
  • A.亨里克森
  • C.维贝里
  • K.克耶加德
  • V.韦斯特法尔斯滕尼克
  • 梁秀龄
  • 丰岩清
  • 叶璐夷
  • 吴梧桐
  • 吴武
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 宋立先; 刘春红; 王占青; 高蓉; 徐学振
    • 摘要: [目的]引进犬MC4R突变点,构建突变体D298N表达载体并在MDCK细胞中获得表达。[方法]设计带突变点D298N引物,以犬MC4R基因组DNA为模板,采用普通PCR和Overlap-PCR扩增编码区,将产物克隆、酶切、测序鉴定。将测序正确的基因连接到pcDNA3.1-myc-His/A载体上,将重组体pcDNA3.1-myc-His/A-cMC4R-D298N酶切、鉴定,将测序正确的重组体转染到MDCK细胞中,继续培养3 d,提取细胞总RNA,并采用RT-PCR方法检测基因表达。提取细胞总蛋白,Western Blot鉴定蛋白表达。[结果]构建带D298N突变点的真核表达载体,提取质粒后有2处碱基不同,分别是777位碱基T→C,892位碱基G→A(引入的突变位点)。转染到MDCK后,RT-PCR和Western Blot均检测到重组体在基因水平和蛋白水平的表达。[结论]成功构建犬的重组体真核表达载体并在MDCK细胞中表达。
    • 侯国顺
    • 摘要: PCR技术应用非常广泛,可用于扩增目的基因,制作探针,引入定点突变,定量检测DNA等.本文通过典型例题介绍了PCR技术的三种题型.一、利用PCR技术进行定点诱变例1通过引物设计运用PCR技术可以实现目的基因的定点突变.
    • 胡培静; 杜媛; 王娅; 王亭忠; 王娟娟; 陈春燕; 马爱群
    • 摘要: 目的:构建并验证 Brugada 综合征相关钠通道 SCN5a 基因 R104W 突变体。方法采用一步法 PCR 突变技术,以 pEGFP-SCN5a 为模板,体外定点诱变构建 pEGFP-SCN5a-R104W 突变体,进行基因测序,并用 Lipofectamine TM3000脂质体转染法转入 HEK293细胞,通过 Western blotting 和膜片钳记录检测蛋白质表达和电流加以验证。结果测序结果显示 SCN5a-R104W 突变体基因序列上第310 C>T,其他序列碱基与野生型相比未发生改变;West-ern blotting 结果显示 SCN5a-R104W 突变体蛋白表达量较野生型 SCN5a 降低;荧光显微镜下显示 SCN5a-R104W 突变体蛋白位于胞质内;SCN5a-R104W 突变体转染后膜片钳记录未能检测到钠电流,且 R104W 突变体对野生型通道有负显性抑制作用。结论成功构建并验证 SCN5a 基因 R104W 突变体。%Objective To construct and verify the R104W mutant of SCN5a channel.Methods The SCN5a-R104W mutant was constructed by rapid site-directed mutagenesis,and the expected mutation was confirmed by direct sequencing.The mutant DNA was transfected into HEK293 cells using Lipofectamine TM3000.Function of the SCN5a-R104W mutant was tested by Western blot analysis and whole-cell patch clamp recording.Results Sequencing results showed that the base on 310 was changed from C to T of SCN5a-R104W mutant DNA.Protein expression of SCN5a-R104W mutant was lower than that of wild-type SCN5a (SCN5a-WT)channel.SCN5a-WT channels were expressed on the cell surface and SCN5a-R104W channels were mainly expressed in the cytoplasm. Patch clamping result showed that no sodium current was recorded from the cells expressing SCN5a-R104W mutant channel,and SCN5a-R104W exerted dominant-negative effect on SCN5a-WT channel.Conclusion Trafficking deficient SCN5a-R104W mutant channel was successfully constructed and verified.
    • 印翠; 张俊玲; 施志仪; 孙文慧; 孙近近
    • 摘要: 以牙鲆空通气孔同源框2基因(empty spiracles homeobox 2,emx2)为例,构建包含emx23'UTR区的野生型和突变型双荧光素酶重组报告表达载体,以期应用于miRNA靶标的检测。利用Trizol法提取牙鲆成鱼精卵巢混合组织总 RNA,参照已克隆出来的emx2基因cDNA序列,设计并合成emx23'UTR片段的引物并进行 PCR扩增,将得到的基因片段和 psiCHECK-2载体双酶切后,用T4 DNA Ligase酶进行连接反应,并转化入 DH5α感受态细胞,筛选后得到野生型重组质粒;同时采用定点诱变法对emx2基因进行体外定点诱变并采用同样的方法形成突变型重组质粒。对野生型和突变型重组质粒进行双酶切、琼脂糖凝胶电泳鉴定及测序分析。成功克隆了emx23'UTR区,并将emx23'UTR区的miRNA靶点序列GACTTGA突变为 AGTCCAG,成功构建了野生型和突变型包含emx23'UTR区的miRNA靶标检测载体。通过RT-PCR、基因重组及定点诱变技术成功构建了应用于miRNA靶标验证的野生型和突变型双荧光素酶报告载体 psiCHECK-emx2-3'UTR和 psiCHECK-mutated-emx2-3'UTR。%TakingParalichthys olivaceus empty spiracles homeobox 2(emx2)as an example, we constructed the wild-type and mutant luciferase reporter plasmids containingemx23'UTR region for being utilized in miRNA target detection. The total RNA was extracted from the mixtures of testis and ovarian in adult fish with Trizol. Using previously-cloned cDNA sequences ofemx2 as a reference, a pair of specific primers foremx23'UTR fragment were designed and synthetized, then amplified genes by RT-PCR and psiCHECK-2 vector were treated with double restriction enzyme digestion, and then ligated with T4 DNA Ligase. The ligated fragment was transformed into the competent cells of DH5α, then the wild-type recombinant plasmid were obtained by screening.In vitro site-directed mutagenesis ofemx2 was carried out, and a site-directed mutant plasmid was generated by the same methods. The results indicated that theemx2 3'UTR ofP. olivaceus was successfully cloned, and GACTTGA, the sequence of miRNA target sites in it was mutated to AGTCCAG. The wild-type and mutant luciferase reporter plasmids used in miRNA target detection were constructed successfully. In conclusion, with the techniques of RT-PCR, gene recombination and site-directed mutagenesis, the wild-type luciferase reporter plasmids psiCHECK-emx2-3'UTR and mutant one of psiCHECK-mutated-emx2-3'UTR used in miRNA target detection were successfully constructed, which lays the foundation for further researches on identification and function of miRNA targetemx2.
    • 刘欣
    • 摘要: 本文对“基因工程”专题中“为什么转入病毒基因可使植物获得抗病毒能力”、“为什么利用基因工程方法能除去猪的抗原决定基因”、“蛋白质工程中怎样实现对目的基因的定向改造”等问题进行了简要解析。
    • 王国丽; DAIHO Takashi; YAMASAKI Kazuo; DANKO Stefania; 王彪; 宿文辉; SUZUKI Hiroshi
    • 摘要: 跨肌浆网膜的钙离子ATP酶SERCA1a可在水解ATP的同时逆浓度梯度从胞浆转运钙离子入肌浆网,引发收缩的骨骼肌细胞舒张.目前对SERCA1a结构与功能的研究,要领先于对其他P型离子转运ATP酶的研究.为了解SERCA1a跨膜螺旋M7与M8膜内侧连接部Linker78(L78)的功能,我们评估了L78部分氨基酸残基突变对SERCA1a反应循环的影响,发现:除G864A之外的所有突变体均可不同程度地降低钙离子转运速率;G862或P863氨基酸残基的突变导致SERCA1a的ATP酶活性显著降低或丧失,并引起由ATP或无机磷酸Pi生成的磷酸化酶中间体EP量显著减少;A893被P取代对SERCA1a的影响与G862、P863突变相似;与野生型SERCA1a相比,G864A与FMQ873-875单突变体ATP酶活性及EP生成量无明显差别.上述结果表明,M7、M8膜内侧连接部L78不仅与跨膜区钙离子转运过程密切相关,而且L78在GPG862-864处及A893附近的正确转折对胞浆结构域P的磷酸化也具有关键的远距离调控作用,提示L78的结构及柔度对SERCA1a构象正常的周期性变化至关重要.
    • 代健; 樊自尧; 杨轩; 张丽萌; 陈战球; 崔玉东
    • 摘要: 金黄色葡萄球菌分泌的α-溶血素是导致肺炎的重要致病因子.为进一步研究金黄色葡萄球菌α-溶血素(α-hla)的分子致病机理以及对其进行免疫预防,对α-hla第35位氨基酸进行了定点突变.用聚合酶链式反应(PCR)技术,从S.aureus wood46株基因组中扩增出α-hla基因,再利用重叠延伸PCR技术,将第35位带正电荷的组氨酸(密码子为CAC)突变为非极性的亮氨酸(密码子为CTC).hlaH35L基因测序结果显示第35位的组氨酸突变为亮氨酸,构建的重组表达质粒pET-28a-c(+)/hla和pET-28a-c (+)/hlaH35L在E.coli BL21 (DE3)中得到表达,重组蛋白α-Hla及hlaH35L大小均为33.4 kDa,α-Hla引起兔红细胞溶血,hlaH35L未引起兔红细胞溶血.成功表达并获得了失去溶血毒性的重组蛋白hlaH35L.
    • 高欢欢; 贺云蕾; 叶璐夷; 王攀; 郭忠慧; 朱自严; 朱永明
    • 摘要: Objective A reliable method for genotyping blood group antigens Dib,k,Jsb1910 and Jsb2019 was developed.Through screening for rare blood types,the National Rare Blood Bank of China may be enriched.Methods The controls for allele detection of blood groups Dib,k,Jsb1910 and Jsb2019 were prepared via polymerase chain reaction (PCR)-mediated gene site-directed mutagenesis (SDM) technique.Sequence-specific primers were designed according to known single nucleotide polymorphism (SNP) sites of alleles of blood groups antigens Dib,k,Jsb1910 and Jsb2019,a multiplex PCR system was developed by optimizing PCR reaction system.And 4190 random healthy donors samples were screened for the blood group antigens.Results Using SDM technique,controls for alleles in blood group Dib,k,Jsb1910 and Jsb2019 were successfully generated.And a multiplex PCR system for genotyping above blood groups was developed.After verification,the system has performed with good stability and reproducibility.Two Di (b-) samples have been discovered from 4190 samples,no k-and Js(b) sample was found.Conclusion Multiplex PCR features rapid detection,high throughput and low cost,and can be used for screening for donors of rare blood types.Information of donors may be registered in a database,which in turn can help those with rare blood types or require long-term blood transfusion to obtain matched blood,thereby reduce the adverse reactions of blood transfusion.%目的 建立可同时检测血型抗原Dib、k、Jsb1910、Jsb2019的一套稳定的基因分型方法,通过筛选获得所检测人群的稀有血型数据,可扩大中国稀有血型资料库.方法 应用基于PCR的基因定点诱变技术制备Dib、k、Jsb1910、Jsb2019血型等位基因检测对照品.分别针对血型抗原Dib、k、Jsb1910、Jsb2019等位基因的单核苷酸多态性位点设计序列特异性引物,通过优化PCR条件建立多重PCR体系,并对4190份随机献血者样本进行Dib、k、Jsb1910、Jsb2019血型抗原基因分型.结果 成功制备出Dib、k、Jsb1910、Jsb2019基因检测对照品,并成功构建检测血型抗原Dib、k、Jsb1910、Jsb2019的多重PCR体系,所建立的多重PCR体系具有良好的重复性和稳定性,4190份随机献血者样本中共检出2例Di(b-)样本,未检出k-和Js(b-)样本.结论 多重PCR具有快捷、高通量且成本低的优点,可用于筛选稀有血型.获得的稀有血型可存入稀有血型数据库,为稀有血型患者及长期输血患者提供相配合的血液,减少输血不良反应的发生.
    • 李岩
    • 摘要: 简介蛋白质工程的基本原理,针对蛋白质工程所应用的不同领域,介绍其研究现状,分析其功能及在人类经济活动中的作用,阐述了蛋白质工程的应用前景,并对于蛋白质工程的研究做出展望.
    • 丁淑琴; 章尧; 陈昌杰; 杨清玲; 程龙强
    • 摘要: Objective:To construct the wild-type and mutant human apolipoprotein M(ApoM) expression plasmid. Methods:The total RNA was extracted from HepG2 cells with Trizol. ApoM gene was amplified by RT-PCR,and inserted into PMD18-T vectors. After ApoM vector was transformed into E. Coli JM109,the positive clones were obtained. Then the recombinant plasmids were identified by restriction enzyme digestion and DNA sequencing. In vitro site-directed mutagenesis was carried out with site-directed mutagenesis kit. Successful site-directed mutagenesis was conformed by DNA sequencing. The wild-type and mutant coding genes were subcloned into prokaryotic expression vector pGEX-KG and eukaryotic expression vector pcDNA3. 1 ( + ) . The recombinant plasmids were transformed into E. Coli DH5α and identified by restriction endonuclease digestion and DNA sequencing. Results: The human ApoM gene was successfully cloned. The wild-type and mutant pGEX-KG-ApoM and pcDNA3. 1 ( + ) - ApoM recombinant plasmids were constructed successfully. Conclusions: With the techniques of RT-PCR, sited-directed mutagenesis and gene recombination, the wild-type and mutant pGEX-KG-ApoM and pcDNA3. 1 ( + ) -ApoM were successfully constructed, which lays the foundation for further investigating the role of ApoM.%目的:构建人载脂蛋白M(ApoM)野生型和突变型原核表达载体pGEX-KG-ApoM及真核表达载体pcDNA3.1(+)-ApoM.方法:Trizol法抽提HepG2细胞总RNA,RT-PCR扩增 ApoM全长基因,将基因片断重组到PMD18-T 质粒中构建PMD18-T-ApoM重组质粒载体,转化到大肠埃希菌JM109后筛选阳性克隆,提取质粒酶切和测序鉴定.采用Sited-directed Mutagenesis定点诱变试剂盒对ApoM基因进行体外定点诱变,DNA测序鉴定定点诱变成功与否.用双酶切方法分别将ApoM野生型和突变型基因定向连接到原核表达载体pGEX-KG和真核表达载体pcDNA3.1(+)中,构建野生型和突变型pGEX-KG-ApoM重组体和pcDNA3.1(+)-ApoM重组体,分别转化到大肠埃希菌DH5α内,提取质粒酶切鉴定和测序鉴定.结果:成功克隆了ApoM并构建了野生型和突变型原核表达载体和真核表达载体.结论:通过 RT- PCR,定点诱变及基因重组技术成功构建野生型和突变型重组表达质粒pGEX-KG-ApoM和pcDNA3.1(+)-ApoM,为进一步研究ApoM的功能奠定了基础.
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