Tufail M, Lee J M, Hatakeyama M, Oishi K, Takeda M
Division of Molecular Science, Graduate School of Science and Technology, Kobe University, Nada, Kobe, Japan.
Arch Insect Biochem Physiol. 2000 Sep;45(1):37-46. doi: 10.1002/1520-6327(200009)45:1<37::AID-ARCH4>3.0.CO;2-8.
A cDNA expression library constructed from poly (A)(+) RNA prepared from vitellogenic female fat body cells of the American cockroach, Periplaneta americana (Dictyoptera) was screened using a polyclonal antiserum against the 100-kD polypeptide(s) from the egg extract. A partial Vg cDNA clone was obtained and sequenced. The 5' end portion of the cDNA was then obtained by the RACE method, cloned, and sequenced. The combined complete Vg cDNA was 5,854 bp long and contained a single ORF encoding 1,896 amino acids. The entire deduced amino acid sequence was aligned confidently with those of the known insect Vgs. A GL/ICG motif, a number of cysteines at conserved locations following this motif, and a DGXR motif upstream of the GL/ICG motif were present near the C-terminal. The chemically determined N-terminal amino acid sequence of the 170-kD polypeptide from the egg extract completely matched the deduced sequence starting from just after one of the consensus (RXXR) cleavage sites, indicating the occurrence of post-translational cleavage in the fat body cells. The Vg gene begins to be expressed in the 2-day-old adult female fat body cells but is never expressed in ovaries or in male fat body cells. Hemolymph Vg was first detected by immunoblotting in 4-day-old adult females, 2 days after the beginning of gene expression. Western blot analysis of major yolk polypeptides in nine cockroach species belonging to the two superfamilies, Blattoidea and Blaberoidea, using the antisera against P. americana major yolk polypeptides showed that the similarities in Vn antigenicity are basically limited to within a superfamily.
用针对美洲大蠊(蜚蠊目)卵黄生成期雌虫脂肪体细胞制备的多聚腺苷酸(poly(A))(+)RNA构建的cDNA表达文库,用针对卵提取物中100-kD多肽的多克隆抗血清进行筛选。获得了一个部分卵黄原蛋白(Vg)cDNA克隆并进行了测序。然后通过RACE方法获得cDNA的5'端部分,进行克隆和测序。合并后的完整Vg cDNA长5854 bp,包含一个编码1896个氨基酸的单一开放阅读框(ORF)。推导的完整氨基酸序列与已知昆虫Vg的序列可靠比对。在C末端附近存在一个GL/ICG基序、该基序后保守位置的多个半胱氨酸以及GL/ICG基序上游的一个DGXR基序。化学测定的卵提取物中170-kD多肽的N末端氨基酸序列与从一个共有(RXXR)切割位点之后开始的推导序列完全匹配,表明在脂肪体细胞中发生了翻译后切割。Vg基因在2日龄成年雌虫脂肪体细胞中开始表达,但在卵巢或雄虫脂肪体细胞中从不表达。通过免疫印迹在4日龄成年雌虫中首次检测到血淋巴Vg,此时基因表达开始2天。使用针对美洲大蠊主要卵黄多肽的抗血清对属于两个总科(蜚蠊总科和鳖蠊总科)的9种蟑螂的主要卵黄多肽进行蛋白质免疫印迹分析表明,卵黄蛋白原(Vn)抗原性的相似性基本上仅限于一个总科内。