49 resultados para Subtelomeric Deletion
Resumo:
rpoS 基因编码RpoS因子(RNA聚合酶的σ亚基),能增强细菌细胞对外界不良环境的抗逆性和适应能力。我们从鳗弧菌(Vibrio anguillarum)M3 Fosmid 文库中得到rpoS 基因序列,全长999bp,同源分析发现与大肠杆菌(Escherichia coli)有71%的相似性,与霍乱弧菌(Vibrio cholerae )有78%的相似性。为了研究rpoS在鳗弧菌中的作用,我们利用in-frame deletion技术构建了rpoS 基因的非极性缺失突变株,同时利用细菌的接合转移,以低拷贝克隆质粒pSUP202为载体,构建了突变株的互补株。 在TSB培养基中,rpoS 基因的缺失减缓了鳗弧菌对数期的生长,但是对稳定期的生长没有影响。对数期鳗弧菌在1M蔗糖(渗透压胁迫)和5%(v/v)乙醇中的生长减缓,而在18%(v/v)乙醇中的生长及42℃热击时的存活率相对于野生型没有变化。不同生长时期的鳗弧菌对15mM H2O2的反应有所不同,rpoS 的缺失使对数期的鳗弧菌对15mM H2O2的反应更加敏感。在rpoS基因互补株中,上述表型几乎恢复到野生型水平。 我们通过感染实验发现,rpoS 基因的缺失使鳗弧菌的LD50提高了20倍。 RpoS的突变对鳗弧菌的泳动和胞外酶的产生也有影响。突变株泳动圈直径是野生型的73.8%,在明胶平板和酪蛋白平板上的透明圈直径分别为野生型的61%和69%。通过azocaseion检测胞外产物ECP酶活发现,突变株的酶活是野生型的35.5%。 以上数据表明了RpoS在鳗弧菌对数期应对外界不良环境时起到了重要作用,同时参与了鳗弧菌的致病过程。
Resumo:
本研究构建了迟缓爱德华氏菌(Edwardsiella tarda)LSE40 基因组fosmid文库,该文库共包含2 500个克隆,插入片段平均大小为33.6kb,文库总容量约84Mb,覆盖E.tarda LSE40基因组(按5Mb计算)超过16倍。随机挑取1 000个fosmid克隆进行双末端测序共得到1 741条高质量的序列,序列平均长度546 bp,全长949 997bp,约为E.tarda基因组的19%。将这些序列提交到KEGG自动注释服务器KAAS对所得序列进行代谢途径分析,得到E.tarda LSE40的KO (KEGG Orthology) 注释。分析结果表明,与代谢途径相关的基因有932条序列,与环境信息处理相关基因283条,与遗传信息处理相关基因220条,与细胞进程和人类疾病相关的基因分别为64条和16条。同时将序列进行BlastX,按照微生物致病性共同主题找到61个毒力相关基因。Fosmid文库的建立和部分基因组序列的生物信息学分析为进一步研究E.tarda LSE40的致病机制、代谢机制和生理生态机制提供了丰富的物质基础。 通过比较基因组的方法,从E.tarda LSE40 fosmid文库克隆到编码寡肽透过酶的opp基因簇,该基因簇全长6 741bp,含有5个ORF,依次编码OppA-B-C-D-F 5个蛋白;位于oppA和oppB的间隔区和oppF之后的非编码区各有一个茎环结构,推测分别为oppA和opp基因簇的转录终止子。以细菌OppA的保守结构域SBP_bac_5构建系统发生树,结果显示E.tarda LSE40与同属细菌E.ictaluri的亲缘关系最近,与肠杆菌科细菌的亲缘关系较近,与革兰氏阳性细菌的亲缘关系较远,表明OppA的SBP_bac_5结构域可作为细菌分类鉴定的依据。 从E.tarda LSE40 fosmid文库克隆aroA基因全序列,该序列全长1 287bp,编码428个氨基酸,与鲶鱼爱德华氏菌(E. ictaluri)氨基酸相似性在94%,与其他肠杆菌科菌如Escherichia coli和Yersinia enterocolitica相似性在73%-74%。通过In-frame deletion构建了E.tarda LSE40 aroA缺失突变株。与野生型相比,aroA突变株的半数致死量LD50提高了62倍。在牙鲆接种~106cfu/ml的E.tarda细菌时,接种野生型细菌的牙鲆在6天内全部死亡,濒死鱼的细菌数达7.97×108cfu/ 100mg;而接种aroA突变株的牙鲆没有出现死亡,28天后检测不到细菌的存在。实验结果为进一步评价aroA突变株作为减毒活疫苗打下了基础。
Resumo:
本文的这部分是以扩展模型为基础,以五种运算为工具,对空值环境下关系数据库的更新处理策略做了深入研究,并给出了相应的算法及算法分析。
Resumo:
In order to study the role of inherited factors and Type A Behavior Pattern (TABP) in the development of CHD, the present study chose the angiotensin I-converting enzyme (ACE) gene as the target gene, and investigated the associations of TABP, the polymorphism of ACE gene with susceptibility to development of CHD in the healthy population and CHD patients from Northern China. 1. Correlation Analysis Between TABP and serum level of ACE in Chinese healthy individuals TABP and serum of ACE were determined in 137 Chinese healthy individuals. The results showed that there was a significant correlation between the scores of CH in TABP invertory and the serum level of ACE. 2 The distribution charicteristics of ACE gene polymorphism frequencies and association with serum level of ACE in Chinese healthy individuals population The polymorphism of ACE gene and serum of ACE were determined in 137 Chinese healthy individuals. The results showed that: the ethnic differences in I/D polymorphism of ACE gene are obvious; deletion polymorphism of the ACE gene is associated with serum ACE level. 3. The relationship between insertion/deletion polymorphism of ACE gene and CHD in a Chinese population I/D polymorphism in intron 16 of the ACE gene was determined by polymerase chain reaction(PCR) in a study of 109 patients with CHD. The results showed: The frequencies of DD genotype(0.39) and D allele(0.63) were higher among the CHD group than among the control subjects(0.12 and 0.42 respectively, P < 0.01). Furthermore, MI and multivessel disease was more strongly associated with (P < 0.01). It is indicated that D allele and DD gentype of ACE might be an important risk factor for CHD, especially for MI or multivessel disease in Chinese population. 4. Correlation Analysis Between Type A Behavior Pattern and the Polymorphism of ACE Gene The polymorphism of ACE gene and type A behavior pattern (TABP) survey were determined in 291 Chinese healthy individuals. The result showed that the higher frequency of rare D allele of an insertion/deletion (I/D) polymorphism of the angiotensin I-converting enzyme (ACE) gene was found in type A behavior individuals compared with type B behavior individuals in 291 healthy individuals; there was a significant correlation between the scores of CH in TABP invertory and DD genotype of the ACE gene. It is suggested that the behavioral attributes of competitiveness, achievement striving, hostility, being irritated easily and impatience may be associated with heredity. 5. Correlation Analysis Between Angiotensin I-Converting Enzyme Gene Polymorphism, Type A Behavior Pattern and Coronary Heart Disease in Chinese The polymorphism of ACE gene and type A behavior pattern (TABP) survey were determined in 109 patients with CHD. The results showed the development of coronary heart disease(CHD) is influenced mainly by the behavioral attributes of competitiveness, achievement striving, hostility, being irritated easily and impatience; the deletion polymorphism of ACE gene may be play a important role in the process of it. 6. Correlation Analysis Between Type A Behavior Pattern Core Components and the Polymorphism of ACE Gene The polymorphism of ACE gene and type A behavior pattern (TABP) survey were determined in1306 Chinese healthy individuals. The results showed that there was a significant correlation between the scores of CH in TABP invertory and DD genotype of the ACE gene. Furthermore, the behavioral attributes of hostility, being irritated easily and impatience may be associated with heredity. At the end of this research, in terms of theory, the research approaches of TABP and the factors influenced the relationship between TABP and CHD were explored and discussed. Furthermore, several new opinions were put forward.