Quantitation of H-pylori cytotoxin mRNA by real-time RT-PCR shows a wide expression range that does not correlate with promoter sequences

被引:9
作者
Ayala, G
Chihu, L
Perales, G
Fierros-Zárate, G
Hansen, LM
Solnick, JV
Sánchez, J
机构
[1] Inst Nacl Salud Publ, Ctr Invest Enfermedades Infecciosas, Cuernavaca 62508, Morelos, Mexico
[2] Univ Calif Davis, Dept Internal Med, Ctr Comparat Med, Davis, CA USA
[3] Univ Calif Davis, Dept Med Microbiol, Ctr Comparat Med, Davis, CA USA
[4] Univ Calif Davis, Dept Immunol, Ctr Comparat Med, Davis, CA USA
[5] Univ Autonoma Estado Morelos, Fac Med, Cuernavaca, Morelos, Mexico
关键词
RT-PCR; mRNA quantitation; promoter differences; multi-modal gene regulation; Mexican Helicobacter pylori;
D O I
10.1016/j.micpath.2004.06.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Up to 28-fold differences in vacA expression in Helicobacter pylori strains grown in vitro were demonstrated by real time quantitative RT-PCR. These large differences in expression were unrelated to putative - 35 and - 10 motifs or to other untranslated sequences upstream of the ATG start site. The lack of correlation between promoter sequences and the vacA expression levels suggest the potential existence of a bacterial strain-specific factor, as earlier proposed by others on the basis of reporter gene fusions. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 167
页数:5
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