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通过RNA干扰在田间种植的杨树中实现高效稳定的转基因抑制

Efficient and stable transgene suppression via RNAi in field-grown poplars.

作者信息

Li Jingyi, Brunner Amy M, Shevchenko Olga, Meilan Richard, Ma Cathleen, Skinner Jeffrey S, Strauss Steven H

机构信息

Department of Forest Science, Oregon State University, Corvallis, OR 97331-5752, USA.

出版信息

Transgenic Res. 2008 Aug;17(4):679-94. doi: 10.1007/s11248-007-9148-1. Epub 2007 Oct 11.

Abstract

The efficiency and stability of RNA interference (RNAi) in perennial species, particularly in natural environments, is poorly understood. We studied 56 independent poplar RNAi transgenic events in the field over 2 years. A resident BAR transgene was targeted with two different types of RNAi constructs: a 475-bp IR of the promoter sequence and a 275-bp IR of the coding sequence, each with and without the presence of flanking matrix attachment regions (MARs). RNAi directed at the coding sequence was a strong inducer of gene silencing; 80% of the transgenic events showed more than 90% suppression. In contrast, RNAi targeting the promoter resulted in only 6% of transgenic events showing more than 90% suppression. The degree of suppression varied widely but was highly stable in each event over 2 years in the field, and had no association with insert copy number or the presence of MARs. RNAi remained stable during a winter to summer seasonal cycle, a time when expression of the targeted transgene driven by an rbcS promoter varied widely. When strong gene suppression was induced by an IR directed at the promoter sequence, it was accompanied by methylation of the homologous promoter region. DNA methylation was also observed in the coding region of highly suppressed events containing an IR directed at the coding sequence; however, the methylation degree and pattern varied widely among those suppressed events. Our results suggest that RNAi can be highly effective for functional genomics and biotechnology of perennial plants.

摘要

人们对多年生植物中RNA干扰(RNAi)的效率和稳定性了解甚少,尤其是在自然环境中。我们在田间对56个独立的杨树RNAi转基因事件进行了为期两年的研究。用两种不同类型的RNAi构建体靶向一个常驻的BAR转基因:一个475bp的启动子序列反向重复序列(IR)和一个275bp的编码序列反向重复序列,每种构建体都有或没有侧翼基质附着区域(MARs)。针对编码序列的RNAi是基因沉默的强诱导剂;80%的转基因事件显示出超过90%的抑制率。相比之下,靶向启动子的RNAi仅导致6%的转基因事件显示出超过90%的抑制率。抑制程度差异很大,但在田间的两年中每个事件都高度稳定,并且与插入拷贝数或MARs的存在无关。在冬季到夏季的季节循环中,RNAi保持稳定,这是由rbcS启动子驱动的靶向转基因表达差异很大的时期。当由靶向启动子序列的反向重复序列诱导出强基因抑制时,会伴随着同源启动子区域的甲基化。在含有靶向编码序列的反向重复序列的高度抑制事件的编码区域也观察到了DNA甲基化;然而,在这些抑制事件中,甲基化程度和模式差异很大。我们的结果表明,RNAi对于多年生植物的功能基因组学和生物技术可能非常有效。

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