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INSECT DIURETIC HORMONSES: STRUCTURES AND FUNCTION

INSECT DIURETIC HORMONSES: STRUCTURES AND FUNCTION
昆虫利尿激素:结构和功能
批准号:
6525675
负责人:
DAVID Allan SCHOOLEY
金额:
$22.42万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1992
资助国家:
美国
项目状态:
已结题
起止时间:
1992-09-30 至 2004-08-31

项目摘要

项目成果

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中文摘要
翻译
昆虫有低压循环系统,需要利尿激素(DH)来控制马氏管的排尿速率。有13个与CRF相关的类似DH,但其结构远比CRF超家族多样。在这个项目中,很明显许多物种有两个DH,它们是相关的,但属于旁系同源物的亚科。我们计划继续调查,以继续调查在疾病载体Rhodnius prolixus中似乎是DH家族的两个成员。激肽是另一个控制利尿的小肽家族。它们具有相当保守的C-末端五肽基序,并已被发现在几种昆虫中与CRF样DH具有协同作用。我们建议从R. prolixus和Manduca sexta;这些昆虫代表了具有不同饮食习惯的物种,前者是专性吸血者,而后者是植食性的。我们计划研究这些肽对两个物种的马氏管的相互作用及其分子作用模式。激肽是另一个控制利尿的小肽家族。它们共享一个相当保守的C-末端五肽基序,并已被发现在几种昆虫中与CRF样DH具有协同效应。我们建议从R. prolixus和Manduca sexta;这些昆虫代表了具有不同饮食习惯的物种,前者是专性吸血者,而后者是植食性的。我们计划研究这种专性供血者和后者是植食性的相互作用。我们计划研究这些肽对两个物种的马氏管的相互作用及其分子作用模式。在先前的授权期间,从蟑螂Diploptera punctata中鉴定出一种特别新颖的DH,沿着CRF样DH。这种新的DH被证明在结构和功能上与脊椎动物中的降钙素相关。肽(Dippu-DH 31)和来自相同物种的CRF样DH具有强烈的协同效应。由于这种肽的高效力,对相关物种有很强的协同作用。由于这种肽对相关昆虫物种的高效力,它很可能构成DH的另一个重要家族。该DH的同源物的存在将在其他物种中进行研究,包括R。冗长这些肽对靶组织的影响的研究将在分子水平上进行。很可能M。sexta的2CRF样DH至少有2个受体;一个受体已被鉴定,并将努力表征其他受体。将通过蛋白质交联和分子生物学方法接近所鉴定的受体上的配体结合位点。
英文摘要
Insects have low pressure circulatory systems and require diuretic hormones (DH) to control rate of urine production by Malpighian tubules. There are 13 similar DH related to CRF, but with far more diverse structures than the CRF superfamily. It has become apparent during this project that many species have two DH which are related but belong to sub-families of paralogues. We plan to continue investigating to continue investigating what appears to be two members of this family of DH in the disease vector Rhodnius prolixus. The kinins are another family of small peptides that control diuresis. They share rather conserved C-terminal pentapeptide motif and have been found to have synergistic effects with the CRF-like DH in several species of insect. We propose to identify kinins from R. prolixus and Manduca sexta; these insects represent species with disparate dietary habits, the former being an obligate blood feeder and the latter being phytophagous. We plan to study the interactions of these peptides on Malpighian tubules of the two species and their molecular mode of action. The kinins are another family of small peptides that control diuresis. They share a rather conserved C-terminal pentapeptide motif and have been found to synergistic effects with the CRF-like DH in several species of insect. We propose to identify kinins from R. prolixus and Manduca sexta; these insects represent species with disparate dietary habits, the former being an obligate blood feeder and the latter being phytophagous. We plan to study the interaction of this obligate blood feeder and the latter being phytophagous. We plan to study the interactions of these peptides on Malpighian tubules of the two species and their molecular mode of action. During the prior grant period a particularly novel DH was identified from a cockroach, Diploptera punctata, along with a CRF-like DH. This new DH proved to be structurally and functionally related to calcitonin in vertebrates. The peptide (Dippu-DH31) and the CRF-like DH from the same species have strongly synergistic effects. Due to the high potency of this peptide on related species have strongly synergistic effects. Due to the high potency of this peptide on related species of insects, it may well constitute an additional important family of DH. The existence of homologues of this DH will be investigated in other species, including R. prolixus. Studies of the effects of such peptides on the target tissue will be pursued at the molecular level. It is probable that M. sexta has at least 2 receptors for its 2CRF-like DH; one receptor has been identified and efforts to characterize other receptors will be pursued. The ligand binding site on the identified receptor will be approached by protein cross-linking and molecular biological approaches.
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Neuropeptide Modulation of Courtship Behaviors
  • 批准号:
    7921851
  • 项目类别:
  • 资助金额:
    $5.55万
  • 财政年份:
    2009
  • 负责人:
    DAVID Allan SCHOOLEY
  • 依托单位:
Neuropeptide Modulation of Courtship Behaviors
  • 批准号:
    7527315
  • 项目类别:
  • 资助金额:
    $43.36万
  • 财政年份:
    2008
  • 负责人:
    DAVID Allan SCHOOLEY
  • 依托单位:
Neuropeptide Modulation of Courtship Behaviors
  • 批准号:
    8101339
  • 项目类别:
  • 资助金额:
    $35.97万
  • 财政年份:
    2008
  • 负责人:
    DAVID Allan SCHOOLEY
  • 依托单位:
Neuropeptide Modulation of Courtship Behaviors
  • 批准号:
    7660351
  • 项目类别:
  • 资助金额:
    $38.01万
  • 财政年份:
    2008
  • 负责人:
    DAVID Allan SCHOOLEY
  • 依托单位:
海外基金