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具有质体中荧光蛋白细胞类型特异性表达的转基因玉米品系。

Transgenic maize lines with cell-type specific expression of fluorescent proteins in plastids.

机构信息

Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.

出版信息

Plant Biotechnol J. 2010 Feb;8(2):112-25. doi: 10.1111/j.1467-7652.2009.00463.x. Epub 2009 Dec 28.

Abstract

Plastid number and morphology vary dramatically between cell types and at different developmental stages. Furthermore, in C4 plants such as maize, chloroplast ultrastructure and biochemical functions are specialized in mesophyll and bundle sheath cells, which differentiate acropetally from the proplastid form in the leaf base. To develop visible markers for maize plastids, we have created a series of stable transgenics expressing fluorescent proteins fused to either the maize ubiquitin promoter, the mesophyll-specific phosphoenolpyruvate carboxylase (PepC) promoter, or the bundle sheath-specific Rubisco small subunit 1 (RbcS) promoter. Multiple independent events were examined and revealed that maize codon-optimized versions of YFP and GFP were particularly well expressed, and that expression was stably inherited. Plants carrying PepC promoter constructs exhibit YFP expression in mesophyll plastids and the RbcS promoter mediated expression in bundle sheath plastids. The PepC and RbcS promoter fusions also proved useful for identifying plastids in organs such as epidermis, silks, roots and trichomes. These tools will inform future plastid-related studies of wild-type and mutant maize plants and provide material from which different plastid types may be isolated.

摘要

质体数目和形态在不同细胞类型和不同发育阶段有很大差异。此外,在玉米等 C4 植物中,叶绿体超微结构和生化功能在叶肉和束鞘细胞中专门化,这些细胞从叶基部的原质体形式向顶端分化。为了开发玉米质体的可见标记物,我们创建了一系列稳定的转基因品系,这些品系表达荧光蛋白与玉米泛素启动子、质体特异性磷酸烯醇丙酮酸羧化酶(PepC)启动子或束鞘特异性 Rubisco 小亚基 1(RbcS)启动子融合。我们对多个独立事件进行了检查,结果表明,经过密码子优化的玉米 YFP 和 GFP 版本表达特别好,并且表达稳定遗传。携带 PepC 启动子构建体的植物在叶肉质体中表现出 YFP 表达,而 RbcS 启动子介导的表达则在束鞘质体中。PepC 和 RbcS 启动子融合也被证明可用于鉴定表皮、丝、根和毛状体等器官中的质体。这些工具将为野生型和突变型玉米植物的未来质体相关研究提供信息,并提供可能分离不同质体类型的材料。

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