Sawada H, Yamahama Y, Yamamoto T, Mase K, Ogawa H, Iino T
Laboratory of Biology, Department of General Studies, College of Humanities and Sciences, Nihon University, Sakurajosui 3-25-40, Setagaya-ku, Tokyo 156-8550, Japan.
Insect Biochem Mol Biol. 2006 Dec;36(12):911-20. doi: 10.1016/j.ibmb.2006.09.002. Epub 2006 Sep 23.
In order to understand the molecular mechanism of development during early embryogenesis in diapause and non-diapause of the silkworm, mRNA from diapause and non-diapause eggs was compared using the differential display technique. We cloned the full length of a cDNA encoding a novel RNA helicase-like (RHL) protein by the RACE method using a cDNA fragment which was one of the specific cDNAs in the non-diapause eggs. A BLAST search using the predicted amino acid sequence of RHL revealed a low homology (21-25% identity of its partial length) with that of the DEAD-box RNA helicase. Gene expression of the RHL gene of the diapause and non-diapause eggs was investigated by RT-PCR until 60h after oviposition. Amplified RHL cDNA was observed through all the stages in the non-diapause eggs, while in the diapause eggs, cDNA was found in eggs 0-12h after oviposition but disappeared 24-60h after oviposition. When the diapause eggs were activated by HCl treatment after chilling at 4 degrees C for 6 days from 48h after oviposition (artificial diapause termination), cDNA was observed from 12h after HCl treatment. We also investigated the immunohistochemical distribution and localization of RHL in non-diapause eggs using anti-recombinant His-tag RHL antiserum. RHL was distributed in blastoderm cells and yolk cells and was localized in the nucleus and the cytosol of yolk cells. These data suggest that RHL has an important role in the early embryo of the silkworm.
为了了解家蚕滞育和非滞育早期胚胎发育的分子机制,利用差异显示技术比较了滞育卵和非滞育卵的mRNA。我们使用非滞育卵中的特异性cDNA片段之一,通过RACE方法克隆了一个编码新型RNA解旋酶样(RHL)蛋白的cDNA全长。使用RHL预测的氨基酸序列进行BLAST搜索,发现其与DEAD-box RNA解旋酶的同源性较低(部分长度的同一性为21-25%)。通过RT-PCR研究了滞育卵和非滞育卵中RHL基因在产卵后60小时内的基因表达。在非滞育卵的所有阶段都观察到了扩增的RHL cDNA,而在滞育卵中,产卵后0-12小时的卵中发现了cDNA,但在产卵后24-60小时消失。当滞育卵在产卵后48小时于4℃冷藏6天后用HCl处理激活(人工终止滞育)时,HCl处理后12小时观察到了cDNA。我们还使用抗重组His-tag RHL抗血清研究了RHL在非滞育卵中的免疫组织化学分布和定位。RHL分布在胚盘细胞和卵黄细胞中,定位于卵黄细胞的细胞核和细胞质中。这些数据表明RHL在家蚕早期胚胎中具有重要作用。