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杜氏盐藻RbcS基因的特性及其在莱茵衣藻中的启动子活性

Characterisation of the Dunaliella tertiolecta RbcS genes and their promoter activity in Chlamydomonas reinhardtii.

作者信息

Walker T L, Becker D K, Collet C

机构信息

Cluster for Molecular Biotechnology, Science Research Centre and CRC for Diagnostics, Queensland University of Technology, GPO Box 2434, Brisbane, QLD, Australia, 4000.

出版信息

Plant Cell Rep. 2005 Mar;23(10-11):727-35. doi: 10.1007/s00299-004-0884-x. Epub 2004 Oct 5.

Abstract

The availability of highly active homologous promoters and terminators is critical in the development of a transformation system for the unicellular microalga Dunaliella tertiolecta. To facilitate transformation of this species, we isolated and characterised two native ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit genes (RbcS) including flanking sequences. The two non-allelic cDNA sequences share approximately 80% identity and have approximately 60% identity to the RbcS genes of Chlamydomonas reinhardtii. The D. tertiolecta RbcS promoter and 3' untranslated regions were shown to drive expression of the bleomycin resistance gene (ble) in C. reinhardtii. This is the first demonstration of a heterologous algal promoter being used to drive transgene expression in C. reinhardtii. In addition, promoter deletions were shown to further increase transformation efficiency.

摘要

对于单细胞微藻杜氏盐藻转化系统的开发而言,高活性同源启动子和终止子的可用性至关重要。为了促进该物种的转化,我们分离并鉴定了两个包括侧翼序列的天然核酮糖-1,5-二磷酸羧化酶/加氧酶小亚基基因(RbcS)。这两个非等位cDNA序列具有约80%的同一性,与莱茵衣藻的RbcS基因具有约60%的同一性。杜氏盐藻RbcS启动子和3'非翻译区被证明可驱动莱茵衣藻中博来霉素抗性基因(ble)的表达。这是首次证明异源藻类启动子可用于驱动莱茵衣藻中的转基因表达。此外,启动子缺失显示可进一步提高转化效率。

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