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Cloning, Characterization and Bioinformatic Analysis of the Gene Encoding the Larval Serum Protein 2 in Diapause of the Onion Maggot, Delia Antiqua
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作者 Jingjing Xu Bin Chen +1 位作者 Zhengbo He Youjin Hao 《Engineering(科研)》 2013年第10期487-490,共4页
The full-length cDNA encoding Larval serum protein 2 (LSp-2) in the onion maggot,Delia antiqua, was cloned and sequenced by rapid ampli?cation of cDNA ends methods. The result showed that the cDNA was 2203 bp long and... The full-length cDNA encoding Larval serum protein 2 (LSp-2) in the onion maggot,Delia antiqua, was cloned and sequenced by rapid ampli?cation of cDNA ends methods. The result showed that the cDNA was 2203 bp long and the open reading frame (ORF) of 2106 bp encoded 701 amino acid with a calculated molecular weight of 80.5 kDa and an isoelectric point of 5.87. The onion maggot LSp-2 shows highest homology (83%) to that ofCalliphora vicinaat amino acid level. Its signal peptides, domains and structures were predicted and analyzed by using bioinformatic methods. The amino acid sequence of LSP-2 suggests that it would be a typical hexamerin. 展开更多
关键词 Delia Antiqua DIAPAUSE larval serum protein 2 CLONING Molecular CHARACTERIZATION BIOINFORMATIC Analysis
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Functional analysis of the larval serum protein gene promoter from silkworm,Bombyx mori. 被引量:13
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作者 TANG Shunming, YI Yongzhu, SHEN Xingjia, ZHANG Zhifang, LI Yiren & HE Jialu Key Laboratory of Silkworm Biotechnology, Ministry of Agriculture, Sericultural Research Institute, Chinese Academy of Agricultural Sci-ences, Zhenjiang 212018, China Correspondence should be addressed to Zhang Zhifang (e-mail: zjsbsri@ public.zj.js.cn) 《Chinese Science Bulletin》 SCIE EI CAS 2003年第23期2611-2615,共5页
The regulation region of larval serum protein gene, Bombyx mori. (BmLSP), consisting of the first intron, the first exon, the central promoter region and 5′-upstream region, is cloned from genomic DNA from the silkwo... The regulation region of larval serum protein gene, Bombyx mori. (BmLSP), consisting of the first intron, the first exon, the central promoter region and 5′-upstream region, is cloned from genomic DNA from the silkworm va-riety of Suju譓inghu. Using PCR and restriction endonu-clease methods, a series of luciferase reporter plasmids, driven by different length of BmLSP promoters, are con-structed. Via the transient expression system in BmN cells, the effects of the regulation elements and foreign insect hor-mones on the BmLSP promoter activity are investigated. The results demonstrate that the promoter activity of BmLSP is 5.8- or 4.4-fold higher than that of BmLSPs whose first in-tron or the element in 5′-upstream region harboring the homologous sequence with the first intron of light-chain fib-roin gene (EHIF) is deleted, respectively, suggesting that both the first intron and EHIF contain the main positive cis-acting elements. However, the inactive mariner transposable ele-ment (MTE) in 5′-upstream region presents a negative effect. Furthermore, the effects of juvenile hormone analogue (JHA) on the BmLSP promoter activity show a typical dose-dependent manner, that is, low concentration treat-ments increase the BmLSP promoter activity and high con-centration treatments decrease it. Meanwhile, insect ecdy-sone (MH) treatments present no significant effect. 展开更多
关键词 桑蚕 血清蛋白基因 抑制核酸内切酶法 荷尔蒙
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野桑蚕、家蚕LSP基因5'侧翼区的克隆与序列分析 被引量:1
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作者 唐顺明 沈兴家 +2 位作者 张志芳 李奕仁 何家禄 《蚕业科学》 CAS CSCD 2003年第2期142-147,共6页
根据已报道的家蚕朝日×东海的幼虫血清蛋白LSP基因序列设计1对引物,以野桑蚕、家蚕苏·菊×明·虎的基因组DNA为模板,分别克隆了野桑蚕、家蚕苏·菊×明·虎的LSP,基因5’侧翼区,约1.9kb,并进行了序列测... 根据已报道的家蚕朝日×东海的幼虫血清蛋白LSP基因序列设计1对引物,以野桑蚕、家蚕苏·菊×明·虎的基因组DNA为模板,分别克隆了野桑蚕、家蚕苏·菊×明·虎的LSP,基因5’侧翼区,约1.9kb,并进行了序列测定与分析。结果表明:克隆的野桑蚕、家蚕苏·菊×明·虎的LSP基因5’侧翼区涵盖了第一内含子、第一外显子、启动子区及其5’上游区;野桑蚕LSP基因5’侧翼区与朝日×东海LSP,基因5’侧翼区的同源性达96.4%,其中第一内含子、第一外显子的同源性分别为91.6%,100%;家蚕苏·菊×明·虎的LSP基因5’侧翼区与朝日×东海LSP基因5’侧翼区的同源性达98.9%,其中第一内含子、第一外显子的同源性都为100%,核心启动子区具有典型的TATA盒,还有数种昆虫脂肪体内组织特异性表达基因的共有序列和推定的激素响应元件等功能元件;野桑蚕的LSP基因启动子的5’上游区(-304~598bp)与J139家蚕丝素轻链基因第一内含子区域(7639~7933bp)的同源性达90.6%,-913~-1383bp为失活的部分水手转座子元件。 展开更多
关键词 野桑蚕 家蚕 LSP基因 5′侧翼区 基因克隆 序列分析 血液蛋白 完全变态
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家蚕血淋巴蛋白的发育变化和BmLSP的纯化 被引量:1
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作者 葛宏华 孙莉宁 张其瑞 《安徽大学学报(自然科学版)》 CAS 2001年第3期91-94,共4页
对 1~ 5龄的家蚕幼虫血淋巴取样 ,通过十二烷基硫酸钠 -聚丙酰胺凝胶电泳(SDS -PAGE)观察并分析家蚕幼虫血淋巴主要蛋白的发育变化 ,对其中的一种主要蛋白即家蚕幼虫血清蛋白 ,通过硫酸铵沉淀、阳离子交换柱层析。
关键词 家蚕 血淋巴 幼虫血清蛋白 BmLSP SDS-PAGE法 发育变化 纯化
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