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家蚕Bmtdh基因的克隆与序列分析

Cloning and Sequence Analysis of Bmtdh Gene in Bombyx mori
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摘要 克隆了家蚕苏氨酸脱氢酶基因(Bmtdh),其cDNA长1 310 bp(No.ABA43639.1),包括227 bp 5′-UTR和1 026 bp的完整开放读码框(ORF)。Bmtdh在家蚕基因组上以单拷贝形式存在,编码342个氨基酸,其Ile29-Val322区域是一个完整的表面异构酶功能域。表达谱分析与EST数据的分析表明,Bmtdh在丝腺和卵巢中的转录水平高于其它组织,并且Bmtdh在家蚕4龄眠期、5龄早期的转录水平也很高,而在卵期(G2胚胎)和1龄早期没有检测到其转录表达,表明Bmtdh基因可能参与了蚕丝蛋白的合成过程。 We cloned and sequenced the cDNA (1 310 bp, accession No. ABA43639. 1) of L-threonine 3-dehydrogenase (TDH) in Bombyx mori. It contains a 227 bp 5' untranslated region( 5'-UTR ), locates on the ge nome as a single copy and encodes a 342-residue protein. The region between Ile29 and Val322 is a complete episomerase domain. The expression profile and EST analysis indicated the mRNA transcription level of Bmtdh gene was higher in silk gland and ovary at the 3^rd day of 5^th instar than that of other tissues. RT-PCR experiments of 11 different development periods showed that high transcription level of Bmtdh gene appeared at the 4^th molting stage, 1^st day and 3^rd day of 5^th instar, but it was not detected in G2 embryo period and at the 2^nd day of 1^st instar. This results suggested the Bmtdh gene maybe involved in the process of silk protein synthesis.
出处 《蚕业科学》 CAS CSCD 北大核心 2007年第4期553-561,共9页 ACTA SERICOLOGICA SINICA
基金 国家自然科学基金项目(编号30400328) 国家重点基础研究发展计划"973"项目(编号2004AA2Z1020) 重庆市自然科学基金项目(编号9067)
关键词 家蚕 苏氨酸脱氢酶基因 丝腺 克隆 序列分析 Bombyx mori L-threonine 3-dehydrogenase gene Silk gland Clone Sequence analysis
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参考文献15

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