ArticleThe Plant cell2005
Functional isolation of novel nuclear proteins showing a variety of subnuclear localizations.
Article in The Plant cell, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
25 citing papers in PubMed, 65 citations in OpenAlex.
- Nuclear Proteomics to Understand the Promotive Effect of Plant-Derived Smoke Solution on Wheat Under Salt Stress.Proteomes · 2026Article
- Advancing knowledge of the plant nuclear periphery and its application for crop science.Nucleus (Austin, Tex.) · 2020Review
- Biolistic Approach for Transient Gene Expression Studies in Plants.Methods in molecular biology (Clifton, N.J.) · 2020Review
- MLKS2 is an ARM domain and F-actin-associated KASH protein that functions in stomatal complex development and meiotic chromosome segregation.Nucleus (Austin, Tex.) · 2019Article
- An iNTT system for the large-scale screening of differentially expressed, nuclear-targeted proteins: cold-treatment-induced nucleoproteins in Rye (Secale cereale L.).BMC genomics · 2016Article
- The intriguing plant nuclear lamina.Frontiers in plant science · 2014Review
- A dynamic meiotic SUN belt includes the zygotene-stage telomere bouquet and is disrupted in chromosome segregation mutants of maize (Zea mays L.).Frontiers in plant science · 2014Article
- Protein interactions at the higher plant nuclear envelope: evidence for a linker of nucleoskeleton and cytoskeleton complex.Frontiers in plant science · 2014Review
- Localization of Daucus carota NMCP1 to the nuclear periphery: the role of the N-terminal region and an NLS-linked sequence motif, RYNLRR, in the tail domain.Frontiers in plant science · 2014Article
- Lamin-like analogues in plants: the characterization of NMCP1 in Allium cepa.Journal of experimental botany · 2013Article
- The GIP gamma-tubulin complex-associated proteins are involved in nuclear architecture in Arabidopsis thaliana.Frontiers in plant science · 2013Article
- Comparative analyses of nuclear proteome: extending its function.Frontiers in plant science · 2013Article
- Identification of potential antisense transcripts in rice using conventional microarray.Molecular biotechnology · 2012Article
- Novel plant SUN-KASH bridges are involved in RanGAP anchoring and nuclear shape determination.The Journal of cell biology · 2012Article
- Dynamics of the plant nuclear envelope and nuclear pore.Plant physiology · 2012Review
- The nuclear envelope in the plant cell cycle: structure, function and regulation.Annals of botany · 2011Review
- Structure and expression of the maize (Zea mays L.) SUN-domain protein gene family: evidence for the existence of two divergent classes of SUN proteins in plants.BMC plant biology · 2010Article
- Differential nuclear envelope assembly at the end of mitosis in suspension-cultured Apium graveolens cells.Chromosoma · 2010Article
- Bringing KASH under the SUN: the many faces of nucleo-cytoskeletal connections.The Journal of cell biology · 2009Review
- MNU-induced mutant pools and high performance TILLING enable finding of any gene mutation in rice.Molecular genetics and genomics : MGG · 2008Article
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.