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cDNA cloning and transcriptional regulation of the vitellogenin receptor from the imported fire ant, Solenopsis invicta Buren (Hymenoptera: Formicidae)

机译:进口火蚁中的卵黄蛋白原受体的cDNA克隆和转录调控(膜翅目:昆虫纲)

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摘要

Receptors that transport vitellogenin into oocytes are of vital importance to egg-laying species because they promote oocyte development. In this study, we describe the cloning of the first hymenopteran vitellogenin receptor (VgR) cDNA. Using reverse transcription polymerase chain reaction (RT-PCR) and both 5?- and 3?- rapid amplification of cDNA ends (RACE), cDNA fragments encompassing the entire coding region of a putative VgR from fire ant (= SiVgR) were cloned and sequenced. The complete SiVgR cDNA has a length of 5764 bp encoding a 1782-residue protein with a predicted molecular mass of 201.3 kDa. The deduced amino acid sequence of the SiVgR revealed that it encoded a protein belonging to the low-density lipoprotein receptor superfamily. The number and arrangement of modular domains of SiVgR are the same as those of mosquito and fruit fly VgRs, except there are only four Class A cysteine-rich repeats in the first ligand binding domain of SiVgR compared to five in the mosquito and fruit fly. The deduced amino acid sequence of the SiVgR exhibited 35% and 31% identity to those of the mosquito and fruit fly VgRs, respectively. Northern blot analysis demonstrated that the 7.4-kb SiVgR mRNA was present only in Northern blot analysis demonstrated that the 7.4-kb SiVgR mRNA was present only in ovaries of reproductive females − both alates (virgins) and queens (mated) and was more abundant in alates. The developmental profile of transcriptional expression was determined by semiquantitative RT-PCR. It showed that the SiVgR transcript increased 6-fold from 0- to 10-days after mating, then remained constant through 30 days. It also showed that the SiVgR transcripts increased with age in alate virgin females. The transcriptional expression of the SiVgR was up-regulated more than two-fold by methoprene, a juvenile hormone analog, as determined by using an in vitro system. This suggested the SiVgR gene is JH regulated.
机译:将卵黄蛋白原转运到卵母细胞中的受体对产卵物种至关重要,因为它们促进卵母细胞的发育。在这项研究中,我们描述了第一个膜翅目卵黄蛋白原受体(VgR)cDNA的克隆。使用逆转录聚合酶链反应(RT-PCR)以及cDNA末端的5′-和3′-快速扩增(RACE),克隆了包含来自火蚁(= SiVgR)的推定VgR整个编码区的cDNA片段,已排序。完整的SiVgR cDNA长度为5764 bp,编码1782个残基蛋白质,预测分子量为201.3 kDa。推导的SiVgR的氨基酸序列表明,它编码的蛋白质属于低密度脂蛋白受体超家族。 SiVgR的模块化结构域的数量和排列与蚊子和实蝇VgR的相同,不同的是,SiVgR的第一个配体结合结构域中只有四个富含A类半胱氨酸的重复序列,而在蚊子和实蝇中只有五个。推导的SiVgR的氨基酸序列与蚊子和实蝇VgR的氨基酸序列分别具有35%和31%的同一性。 Northern印迹分析表明仅在生殖雌性卵巢中存在7.4kb SiVgR mRNA,Northern印迹分析表明仅在生殖雌性卵巢中存在7.4kb SiVgR mRNA-迟来的(初生的)卵巢和皇后的(交配的)卵巢中均存在。骨灰通过半定量RT-PCR确定转录表达的发育概况。结果表明,SiVgR转录本在交配后0到10天增加了6倍,然后在30天内保持不变。它也表明,SiVgR转录本随年龄增长而增加。通过使用体外系统测定,甲氧戊二烯(一种少年激素类似物)将SiVgR的转录表达上调了两倍以上。这表明SiVgR基因受JH调控。

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    Chen Mei-Er;

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  • 年度 2005
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