Tian Zongcheng, Zhou Bo, Qian Airong, Xu Huiyun, Di Shengmeng, Zhao Yunpo, Zhang Yuping, Liu Jia, Huang Yongping, Shang Peng
Key Laboratory for Space Biosciences and Biotechnology, Institute of Special Environmental Biophysics, Faculty of Life Sciences, Northwestern Polytechnical University, Xi'an 710072, China.
Sheng Wu Gong Cheng Xue Bao. 2008 Dec;24(12):2041-8.
The full length cDNA of silkworm hibadh gene was cloned by RT-PCR and RACE (Rapid amplification of cDNA ends) technique. The hibadh gene and its deduced amino acid sequences were analyzed. The tissue distribution of hibadh gene in 5th instar silkworm larvae was tested by RT-PCR. The expression patterns of hibadh gene in simulated weightless environment were analyzed by real time RT-PCR. The results showed that the full length hibadh cDNA sequence was 1074 bp in lenth, including an open read frame of 969 bp encoding the entire coding region of Hibadh (GenBank accession No. EU719652). The deduced amino acid sequence similarities of hibadh between silkworm and Burkholderia ambifaria, Drosophila melanogaster, Apis mellifera, Xenopus tropicalis, Mus musculus, Homo sapiens were 46%, 43%, 48%, 44%, 45%, 45%, respectively. Signal peptide analysis showed that Hibadh was a secretory protein. There wasn't glycosyl-phosphatidyl inositol anchor site in Hibadh amino acid sequence. Molecular weight and isoelectric point of Hibadh were 34.1 kD and 9.14 respectively. The RT-PCR tests indicated that the hibadh gene expressed in head, silk gland, midgut, cuticle, blood, fat body, tuba malpighii of the 5th instar silkworm larvae. There were different expression patterns of hibadh gene during different silkworm embryo period in simulated weightless environment. Simulated weightlessness resulted in the expression of silkworm hibadh gene up regulated 2.3-fold (P < 0.05), up regulated 4.6-fold (P<0.01), down regulated 7.6-fold (P < 0.01), down regulated 2.6-fold (P < 0.05) during apophysis formation period, inverse period, trachea formation period, and whole embryo period, respectively. There was no significant change of hibadh gene expression during other period of silkworm embryo between simulated weightless and control groups. There were different response patterns to simulated weightless environment between hibadh gene and whole body of silkworm. Gene showed much higher sensitivity compared to whole body in response to environment. This study is useful for the further research on the gravity biological mechanism of hibadh gene.
采用RT-PCR和RACE(cDNA末端快速扩增)技术克隆了家蚕hibadh基因的全长cDNA。对hibadh基因及其推导的氨基酸序列进行了分析。通过RT-PCR检测了hibadh基因在5龄家蚕幼虫中的组织分布。采用实时RT-PCR分析了hibadh基因在模拟失重环境中的表达模式。结果表明,hibadh cDNA全长序列为1074bp,其中包含一个969bp的开放阅读框,编码Hibadh的整个编码区(GenBank登录号:EU719652)。家蚕hibadh与洋葱伯克霍尔德菌、黑腹果蝇、意大利蜜蜂、热带爪蟾、小家鼠、智人的推导氨基酸序列相似性分别为46%、43%、48%、44%、45%、45%。信号肽分析表明,Hibadh是一种分泌蛋白。Hibadh氨基酸序列中不存在糖基磷脂酰肌醇锚定位点。Hibadh的分子量和等电点分别为34.1kD和9.14。RT-PCR检测表明,hibadh基因在5龄家蚕幼虫的头部、丝腺、中肠、表皮、血液、脂肪体、马氏管中表达。在模拟失重环境下,家蚕胚胎不同时期hibadh基因有不同的表达模式。模拟失重导致家蚕hibadh基因在蜕皮形成期、反转期、气管形成期和全胚期的表达分别上调2.3倍(P<0.05)、上调4.6倍(P<0.01)、下调7.6倍(P<0.01)、下调2.6倍(P<0.05)。在模拟失重组和对照组之间,家蚕胚胎其他时期hibadh基因表达无显著变化。hibadh基因与家蚕整体对模拟失重环境有不同的响应模式。基因对环境的响应比整体表现出更高的敏感性。本研究为进一步研究hibadh基因的重力生物学机制提供了参考。