Moriguchi Kazuki, Suzuki Tadzunu, Ito Yukihiro, Yamazaki Yukiko, Niwa Yasuo, Kurata Nori
Plant Genetics Laboratory, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan.
Plant Cell. 2005 Feb;17(2):389-403. doi: 10.1105/tpc.104.028456. Epub 2005 Jan 19.
Nuclear proteins play key roles in the fundamental regulation of genome instability, the phases of organ development, and physiological responsiveness through gene expression. Although nuclear proteins have been shown to account for approximately one-fourth of total proteins in yeast, no efficient method to identify novel nuclear proteins has been applied to plants. In this study, a trial to isolate nuclear proteins in rice was attempted, and several novel nuclear proteins showing a variety of subnuclear localizations were identified. The nuclear transportation trap (NTT) system, which is a modified two-hybrid system, isolated many nuclear proteins from rice (Oryza sativa) NTT cDNA libraries. Nuclear localization of the isolated proteins was confirmed by transient introduction of green fluorescent protein fusion constructs for a subset of protein genes into onion (Allium cepa) cells. The majority of these proteins, including novel proteins and proteins initially categorized as cytoplasmic proteins, were revealed to be localized in the nucleus. Detailed characterization of unknown proteins revealed various subnuclear localizations, indicating their possible association with chromatin and the nuclear matrix with a foci or speckle-like distribution. Some also showed dual distribution in the nucleus and cytoplasm. In the novel protein fraction, a protein was further identified for its chromatin-associated localization in a specific organ of rice by immunostaining. Thus, a variety of novel nuclear architectural proteins with chromatin or matrix associating abilities, which are important in nuclear organization by influencing certain organ developments or cell responsiveness, can be isolated using the NTT method. Because nuclear proteins other than transcription regulators have rarely been characterized in plants, such as matrix proteins and development-specific chromatin proteins, their identification and subsequent characterization could provide important information for genome-wide regulatory mechanisms controlled by nuclear organization.
核蛋白在基因组不稳定性的基本调控、器官发育阶段以及通过基因表达实现的生理反应中发挥着关键作用。尽管在酵母中核蛋白已被证明约占总蛋白的四分之一,但尚未有高效方法应用于植物中鉴定新型核蛋白。在本研究中,尝试在水稻中分离核蛋白,并鉴定出了几种显示出多种核内亚定位的新型核蛋白。核运输陷阱(NTT)系统是一种改良的双杂交系统,从水稻(Oryza sativa)NTT cDNA文库中分离出了许多核蛋白。通过将一部分蛋白基因的绿色荧光蛋白融合构建体瞬时导入洋葱(Allium cepa)细胞,证实了分离蛋白的核定位。这些蛋白中的大多数,包括新型蛋白和最初归类为细胞质蛋白的蛋白,都被发现定位于细胞核中。对未知蛋白的详细表征揭示了各种核内亚定位,表明它们可能与染色质和核基质相关,呈斑点状或点状分布。有些蛋白在细胞核和细胞质中也呈现双重分布。在新型蛋白组分中,通过免疫染色进一步鉴定了一种蛋白在水稻特定器官中的染色质相关定位。因此,利用NTT方法可以分离出多种具有染色质或基质结合能力的新型核结构蛋白,这些蛋白通过影响特定器官发育或细胞反应在核组织中起重要作用。由于除转录调节因子外的核蛋白在植物中很少被表征,如基质蛋白和发育特异性染色质蛋白,它们的鉴定及后续表征可为由核组织控制的全基因组调控机制提供重要信息。