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Roles of reverse transcriptase and its cDNA product as new virulence factors in Vibrio infectious disease

Roles of reverse transcriptase and its cDNA product as new virulence factors in Vibrio infectious disease
逆转录酶及其cDNA产物作为弧菌感染性疾病新毒力因子的作用
批准号:
13670273
负责人:
SHIMAMOTO Tadashi
金额:
$2.3万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2001
资助国家:
日本
项目状态:
已结题
起止时间:
2001 至 2002

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中文摘要
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英文摘要
Bacterial reverse transcriptase is responsible for the synthesis of satellite RNA-DNA complex called multicopy single-stranded DNA (msDNA).A genetic element required for the msDNA synthesis is named return which consists of the msr-msd region, a coding region for the msDNA and the ret gene, a coding region for reverse transcriptase. Although the role(s) of return and msDNA remains unclear, it has been reported that mutation frequency was increased in Escherichia coil under conditions in which msDNA was overproduced in a cell.To date, we have demonstrated the existence of msDNA in some Vibrio species, such as V. choleras, V. parahaemolyticus, and so on, and cloned the return regions from their chromosomes, msDNAs have also been found in other pathogenic bacteria, such as enteropathogenic E. coil, Salmonella, and so on. A relationship between msDNA and / or reverse transcriptase and bacterial pathogenicity has been suggested recently.In V. choleras, only O1 and O139 serogroups are the causative agents of epidemic cholera and all the other non-O1 / non-O139 strains are not basically associated with epidemic cholera. In this study, to investigate the relationship between msDNA and / or reverse transcriptase and pathogenictiy in V. choleras, we examined the existence of msDNA and return in different serogroups of V. cholera. Thus we found that all O1 and O139 strains we have tested produced the same msDNA in length. However, non-O1 / non-O139 strains do not contain msDNA, meaning that a relationship between pathogenicity of V.cholerae and msDNA and / or reverse transcriptase was strongly indicated. In addition, the same return is inserted into the same integration site of the O1 and O139 strains. On the other hand, several fragments of different length replace the return in the non-O1 / non-139 strains.
期刊论文(6)
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会议论文
K.Yamanaka: "Mobile DNA II"ASM Press. 1204 (2002)
K.Yamanaka:“Mobile DNA II”ASM Press。
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K.Yamanaka: "Mobile DNA II"ASM Press (in press). (2002)
K.Yamanaka:“Mobile DNA II”ASM Press(正在印刷中)。
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島本 整: "細菌の逆転写酵素およびmsDNAの構造と機能"日本細菌学雑誌. 58(印刷中). (2003)
Sei Shimamoto:“细菌逆转录酶和 msDNA 的结构和功能”,日本细菌学杂志 58(出版中)。
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Kunitoshi Yamanaka,: "Returns"Mobile DNA II. 784-795 (2002)
山中邦俊:《归来》机动DNA II。
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6
    Regulation of virulence expression by retron including reverse transcriptase gene and roles as mobile genetic elements
    • 批准号:
      22390083
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.9万
    • 财政年份:
      2010
    • 负责人:
      SHIMAMOTO Tadashi
    • 依托单位:
    Multidrug resistance mechanism of pathogenic bacteria by mobile genetic elements
    • 批准号:
      18590426
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.53万
    • 财政年份:
      2006
    • 负责人:
      SHIMAMOTO Tadashi
    • 依托单位:
    Functional analysis of bacterial reverse transcriptase genes and retroelements in pathogenic bacteria
    • 批准号:
      15590388
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2003
    • 负责人:
      SHIMAMOTO Tadashi
    • 依托单位:
    海外基金