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71.
赖型钩体flaB2与VR1012中的CpG基序分析 总被引:3,自引:0,他引:3
目的:对问号赖型钩端螺旋体(赖型钩体)DNA疫苗[包括内鞭毛蛋白基因(flaB2)和质粒DNA表达载体(VR1012)]的CpG基序(CpG motifs)进行分析,为DNA疫苗免疫机制的阐明和提高DNA疫苗的效能奠定基础。方法:以flaB2与VR1012构建重组DNA的免疫原,对flaB2及VR1012全核苷酸序列进行计算机分析(分类、计数和定位)。结果:CpG的“C”的侧翼为两个嘌呤,“G”的侧翼为两个嘧啶,在flaB2中共3个,分别为GACGCT,GACGTC和GACGCC;在VR1012中共11个,分别为GACGTC1个,GACGCT2个,GACGCC1个,GACGTT1个,GGCGTT2个,GGCGCT2个,GGCGCC1个,AACGCT1个,其中特别重要的TGACGTCA4个和TAACGCCA有1个,位于5'端456-463;509-516;592-599;778-785和486-493;4个TGACGTCA和1个TAACGCCA均位于5'端且相对集中。结论:赖型钩体flaB2与VR1012构成的DNA疫苗含有TGACGTCA等CpG,这些基序又称免疫刺激序列,构成了DNA疫苗中的佐剂。 相似文献
72.
73.
TSG-6基因在3T3-L1脂肪细胞诱导分化中表达水平的变化 总被引:2,自引:0,他引:2
[目的] 探讨TSG-6基因在3T3-L1脂肪细胞诱导分化中表达水平的变化。[方法] 采用细胞培养和RT-PCR技术,检测细胞诱导分化不同时段脂肪细胞中TSG-6基因的表达水平。[结果] ①随着脂肪细胞逐渐分化成熟,TSG-6基因mRNA表达水平逐渐升高;②TSG-6基因表达水平除在细胞分化第0-2d、第3-5d和第7-10d各时段内差异无显著性(P>0.05)外,其余各时段之间表达水平差异均有显著性(P<0.05)。[结论] TSG-6基因与细胞分化以及脂原形成可能相关。 相似文献
74.
泪腺肿瘤中P53蛋白表达的意义 总被引:4,自引:0,他引:4
目的了解P53基因在泪腺肿瘤的表达及其临床病理学意义。方法应用免疫组织化学ABC法检测57例泪腺上皮性肿瘤患者和10例正常人泪腺组织中P53蛋白的表达情况,并与病理分级、复发相联系。结果10例正常人泪腺组织中P53表达全部为阴性;恶性肿瘤患者的表达率为48.6%,良性肿瘤中P53达率为18%,二者相比有显著性差异(P<0.025);复发患者阳性率为76.9%,明显高于未复发患为31.8%(P=0.015)。结论P53基因参与了泪腺肿瘤的发生发展并与肿瘤的分化和复发有关。 相似文献
75.
将医用缝合线浸泡在质粒DNA溶液中,然后缝合在大鼠股四头肌上,可以观察到外源基因在肌肉组织中高效、稳定地表达,其表达量高于磷酸钙共沉淀和DNA沉淀块埋植法,较肌肉直接注射法表达量高10倍左右。 相似文献
76.
Chihaya Maesawa Gen Tamura Yasushi Suzuki Kaoru Ishida Kazuyoshi Saito Ryoichi Satodate 《Cancer science》1992,83(12):1253-1256
For the rapid and sensitive detection of p53 gene mutations in esophageal endoscopic biopsy specimens, we combined cell sorting with the polymerase chain reaction and single-strand conformation polymorphism (PCR-SSCP) analysis. Mutations in exons 5–8 of the p53 gene were investigated by FCR-SSCF analysis using 103 sorted nuclei obtained from each endoscopic biopsy specimen of 16 patients with esophageal cancer. DNAs extracted from their respective surgical specimens were investigated by a conventional method of PCR-SSCP analysis. Mutations in the biopsy specimens were detected in 6 of the 12 aneuploid tumors but in none of the 4 diploid tumors. After tumor cell enrichment by cell sorting, one mutation in exon 8 became apparent, which could not be detected from the surgical specimen by a conventional method of PCR-SSCP analysis. This method should improve the sensitivity of detecting p53 gene mutations, and provides additional information concerning the DNA ploidy pattern in the tumors. 相似文献
77.
A murine monoclonal antibody (MDR3M) (isotype: IgM) reactive with mdr3 gene product was generated by immunizing mice with mdr3 -specific peptide (H2 N-12 WRPTSAEGDFELGISSKQKRKKTKTVKMI41 G-COOH) and hybridizing the primed mouse splenic B cells with X63-Ag8,6.5.3 mouse plasmacytoma cells. MDR3M did not cross-react with mdr1 gene product. This monoclonal antibody may be useful for analyzing the role of mdr3 gene product in cells and tissues. 相似文献
78.
Summary;To investigate the distribution of possible novel mutations from parkin gene in variant sub-set of patients with Parkinson’s disease(PD)in China and explore whether parkin gene plays an im-portant role in the pathogenesis of PD,70 patients were divided into early-onset group and late-onsetgroup; 70 healthy subjects were included as controls.Genomic DNA from 70 normal controls andfrom those of PD patients were extracted from peripheral blood leukocytes by using standard proce-dures.Mutations of parkin gene(exon 1—12)in all the subjects were screened by PCR-single strandconformation polymorphism(SSCP),and further sequencing was performed in tue samples with ab-normal SSCP results,in order to confirm the mutation and its location.A new missense mutationGly284Arg in a patient and 3 abnormal bands in SSCP electrophoresis from samples of another 3 pa-tients were found.All the DNA variants were sourced from the samples of the patients with early-on-set PD.It was concluded that Parkin point mutation a 相似文献
79.
80.
S E Irwin G Y Kwei G R Blackburn R Thurman F C Kauffman 《Environmental and molecular mutagenesis》1992,19(3):253-258
Comparison of the mutagenicity of nine isomeric benzo(a)pyrenyl [B(a)P] phenols conjugated with either sulfate or glucuronide was carried out using strain Salmonella typhimurium TA98. Of the nine conjugates tested, only B(a)P-1-sulfate was mutagenic. Accordingly, the mutagenicity of B(a)P-1-sulfate was compared with that of B(a)P and 1-hydroxybenzo(a)pyrene [B(a)P-1-OH] in the presence and absence of rat lung S9 and Aroclor-induced liver S9 with and without an NADPH-generating system. B(a)P-1-sulfate was slightly mutagenic, whereas B(a)P and the 1-hydroxy derivative were nonmutagenic when S9 fractions and NADPH were omitted. Addition of induced liver S9 with NADPH caused mutagenicity with B(a) -1-OH greater than B(a)P greater than B(a)P-1-sulfate. B(a)P-1-sulfate was the only mutagenic species when lung S9 was added. This mutagenicity did not require NADPH. Sodium sulfite, an inhibitor of arylsulfatase, decreased the mutagenicity of B(a)P-1-sulfate. These data suggest that a unique mutagenic species is generated from B(a)P-1-sulfate via arylsulfatase in rat lung. 相似文献