van Heusden M C, Thompson F, Dennis J
Institute of Parasitology of the Czech Academy of Sciences, Ceské Budĕjovice, Czech Republic.
Insect Biochem Mol Biol. 1998 Oct;28(10):733-8. doi: 10.1016/s0965-1748(98)00068-x.
The biosynthesis of lipophorin of the yellow fever mosquito, Aedes aegypti, was investigated. Fat bodies were incubated in vitro with radiolabeled methionine and cysteine, and radiolabeled proteins secreted into the medium were analyzed by density gradient ultracentrifugation, SDS-PAGE and fluorography. Lipophorin was synthesized in the fat body and secreted into the medium. Its density was 1.114 g/ml, similar to that of lipophorin circulating in hemolymph. Three peptides of a tryptic digest of apolipophorin II were sequenced and degenerate oligonucleotide primers were designed based on the amino acid sequences. With these primers, a cDNA product of 1.2 kb was amplified by RT-PCR using as template RNA extracted from adult female mosquitoes 24 h after ingestion of a blood meal. This cDNA was cloned, sequenced and used as a probe for Northern blot analysis, which revealed that the apoproteins of lipophorin were coded for by a single mRNA of approximately 10 kb. The expression of the apolipophorins was induced by blood feeding. From the data presented we concluded that Aedes aegypti lipophorin is synthesized in the fat body and that the expression of its apolipophorins is induced by blood feeding.
对黄热病蚊子埃及伊蚊的脂磷蛋白生物合成进行了研究。将脂肪体与放射性标记的蛋氨酸和半胱氨酸进行体外孵育,通过密度梯度超速离心、SDS-PAGE和荧光自显影分析分泌到培养基中的放射性标记蛋白。脂磷蛋白在脂肪体中合成并分泌到培养基中。其密度为1.114 g/ml,与血淋巴中循环的脂磷蛋白密度相似。对脱辅基脂蛋白II的胰蛋白酶消化产物的三个肽段进行了测序,并根据氨基酸序列设计了简并寡核苷酸引物。使用这些引物,以摄取血餐后24小时的成年雌性蚊子提取的RNA为模板,通过RT-PCR扩增出1.2 kb的cDNA产物。该cDNA被克隆、测序并用作Northern印迹分析的探针,结果显示脂磷蛋白的载脂蛋白由一个约10 kb的单一mRNA编码。血餐诱导载脂蛋白的表达。根据所提供的数据,我们得出结论,埃及伊蚊脂磷蛋白在脂肪体中合成,其载脂蛋白的表达由血餐诱导。