首页> 外文期刊>Insect Molecular Biology >Fat body expressed yolk protein genes in Hyphantria cunea are related to the YP4 follicular epithelium yolk protein subunit gene of pyralid moths
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Fat body expressed yolk protein genes in Hyphantria cunea are related to the YP4 follicular epithelium yolk protein subunit gene of pyralid moths

机译:小菜蛾脂肪体表达的卵黄蛋白基因与萤火虫的YP4卵泡上皮卵黄蛋白亚基基因相关。

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摘要

cDNA clones for two of the yolk proteins, YP1 and YP2, produced by the fat body of the moth, Hyphantria cunea, were sequenced and found to be homologous to the follicular epithelium yolk proteins of pyralid moths. Both cDNA clones coded for polypeptides; of 290 residues and the deduced amino acid sequence identity between YP1 and YP2 was very high (79.0%). Analysis of the secondary structure of the predicted polypeptides suggests that YP1 and YP2 do not form heteromeric proteins because of differences in secondary structure due to the lack of alpha helices in YP1. Northern blot analysis showed that the transcripts for YP1 (1.2 kb) and YP2 (1.1 kb) were present primarily in the female fat body with only trace levels detectable in the ovary of the adult female. In a developmental study, the YP1 and YP2 transcripts were first detectable in 10-day-old pupae and increased into the adult stage. These results suggest that the YP1 and YP2 genes in H. cunea have been recruited to replace the vitellogenin gene as the primary source of yolk proteins. During this process they have acquired a modified pattern of expression that is different from homologous genes reported in pyralid moths. The assessment of the evolution of proteinaceous yolk in these moths should serve as an excellent model for the evolution of gene recruitment.
机译:对由蛾的脂肪体豚鼠(Hyphantria cunea)产生的卵黄蛋白中的两种卵黄蛋白(YP1和YP2)的cDNA克隆进行了测序,发现它们与拟南芥蛾的卵泡上皮卵黄蛋白同源。两个cDNA克隆均编码多肽。 290个残基的氨基酸残基和推导的YP1和YP2之间的氨基酸序列同一性很高(79.0%)。对预测多肽的二级结构的分析表明,YP1和YP2不会形成异聚蛋白,因为由于YP1中缺少α螺旋,二级结构存在差异。 Northern印迹分析显示YP1(1.2 kb)和YP2(1.1 kb)的转录本主要存在于女性脂肪体内,而在成年女性的卵巢中仅可检测到痕量水平。在一项发育研究中,首先在10天大的p中检测到了YP1和YP2转录本,并增加到成年期。这些结果表明,已经招募了豚鼠中的YP1和YP2基因来代替卵黄蛋白原基因作为卵黄蛋白的主要来源。在此过程中,他们获得了一种修饰的表达模式,该模式不同于吡咯类蛾中报道的同源基因。这些飞蛾中蛋白质卵黄的进化评估应该成为基因募集进化的一个极好的模型。

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