Geminivirus-induced gene silencing of the tobacco retinoblastoma-related gene results in cell death and altered development

被引:32
作者
Jordan, Chad V.
Shen, Wei
Hanley-Bowdoin, Linda K.
Robertson, Dominique
机构
[1] N Carolina State Univ, Dept Plant Biol, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Mol & Struct Biochem, Raleigh, NC 27695 USA
基金
美国国家科学基金会;
关键词
DNA VIGS; retinoblastoma-related protein; cell death; geminivirus; hyperplasia; cell differentiation;
D O I
10.1007/s11103-007-9206-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The retinoblastoma-related protein (RBR) is required for cell cycle control and differentiation and is expressed throughout the life of plants and animals. In this study, the tomato golden mosaic virus (TGMV) geminivirus vector was used to silence NbRBR1 in Nicotiana benthamiana by microprojectile bombardment into fully developed leaves. Similar to previous results using agroinoculation of a tobacco rattle virus silencing vector [Park et al. (Plant J 42:153, 2005)], developmental defects caused by disruptions in cell size and number were seen in new growth. Leaf midvein cross-sections showed tissue-specific differences in size, cell number, and cell morphology. While cortical cell numbers decreased, size increased to maintain overall shape. In contrast, xylem parenchyma cells increased approximately three fold but remained small. Normally straight flowers often curved up to 360 degrees without a significant change in size. However, the most striking phenotype was cell death in mature cells after a delay of 3-4 weeks. Trypan blue staining confirmed cell death and demonstrated that cell death was absent in similarly treated leaves of wild type TGMV-inoculated plants. Quantitative RT-PCR confirmed that the mature TGMV:RBR-inoculated leaves still maintained reduced accumulation of RBR transcript at 4 weeks compared to controls. The results suggest that either inappropriate activation of the cell cycle is lethal in plants or that RBR has other functions, unrelated to the cell cycle. The results also demonstrate that continual transcription of RBR is necessary for cell survival.
引用
收藏
页码:163 / 175
页数:13
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