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首页> 外文期刊>Insect Molecular Biology >Molecular cloning, characterization and tissue expression of prophenoloxidase cDNA from the mosquito Armigeres subalbatus inoculated with Dirofilaria immitis microfilariae
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Molecular cloning, characterization and tissue expression of prophenoloxidase cDNA from the mosquito Armigeres subalbatus inoculated with Dirofilaria immitis microfilariae

机译:接种Dirofilaria微丝itis虫的亚蚊的原酚氧化酚酶原cDNA的分子克隆,鉴定和组织表达

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摘要

A cDNA encoding A. subalbatus prophenoloxidase (As-pro-PO) was obtained by rapid amplification of cDNA ends-polymerase chain reaction (RACE-PCR) after D. immitis inoculation. The 2205 bp As-pro-PO cDNA contains a 32 bp 5'-noncoding region, a 2055 bpopen reading frame (685 amino acids), and a 118 bp 3'-noncoding region. Hydrophobic signal peptide for the endoplasmic reticulum targeting is not found in the NH2-terminal region. Two potential copper-binding domains, amino acids 197-245 and 345-412, are highly homologous to those of the other insect pro-POs. A 2.2 kb As-pro-PO transcript was identified by Northern blot analysis using D. immitis microfilariae-inoculated A. subalbatus. Both in situ hybridization and Northern blot analysis demonstrated that As-pro-PO mRNA was synthesized in mosquito haemocytes, but not in other tissues, i.e. fat bodies, midguts and ovaries, etc.
机译:接种D.炎性炎球菌后,通过快速扩增cDNA末端聚合酶链反应(RACE-PCR)获得了编码白点曲霉前酚氧化酶(As-pro-PO)的cDNA。 2205 bp的As-pro-PO cDNA包含32 bp的5'非编码区,2055 bp的开放阅读框(685个氨基酸)和118 bp的3'非编码区。在NH2末端区域找不到用于内质网靶向的疏水信号肽。两个潜在的铜结合域,氨基酸197-245和345-412,与其他昆虫pro-PO的氨基酸高度同源。通过使用D.线虫病微丝aria菌接种的A.subalbatus的Northern印迹分析鉴定了2.2kb As-pro-PO转录物。原位杂交和Northern印迹分析均表明,As-pro-PO mRNA是在蚊子的血细胞中合成的,但不是在其他组织(即脂肪体,中肠和卵巢等)中合成的。

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