关键词: Agronomic trait OsNMD3 dominant negative ribosome biogenesis rice translational efficiency.

Mesh : Amino Acid Sequence Cell Nucleus / metabolism Cytoplasm / metabolism Gene Expression Regulation, Developmental Gene Expression Regulation, Plant Molecular Sequence Data Oryza / genetics growth & development metabolism Phenotype Phylogeny Plant Proteins / chemistry genetics metabolism Plants, Genetically Modified / chemistry genetics metabolism RNA-Binding Proteins / chemistry genetics metabolism Real-Time Polymerase Chain Reaction

来  源:   DOI:10.1093/jxb/eru150

Abstract:
The ribosome is the basic machinery for translation, and biogenesis of ribosomes involves many coordinated events. However, knowledge about ribosomal dynamics in higher plants is very limited. This study chose a highly conserved trans-factor, the 60S ribosomal subunit nuclear export adaptor NMD3, to characterize the mechanism of ribosome biogenesis in the monocot plant Oryza sativa (rice). O. sativa NMD3 (OsNMD3) shares all the common motifs and shuttles between the nucleus and cytoplasm via CRM1/XPO1. A dominant negative form of OsNMD3 with a truncated nuclear localization sequence (OsNMD3(ΔNLS)) was retained in the cytoplasm, consequently interfering with the release of OsNMD3 from pre-60S particles and disturbing the assembly of ribosome subunits. Analyses of the transactivation activity and cellulose biosynthesis level revealed low protein synthesis efficiency in the transgenic plants compared with the wild-type plants. Pharmaceutical treatments demonstrated structural alterations in ribosomes in the transgenic plants. Moreover, global expression profiles of the wild-type and transgenic plants were investigated using the Illumina RNA sequencing approach. These expression profiles suggested that overexpression of OsNMD3(ΔNLS) affected ribosome biogenesis and certain basic pathways, leading to pleiotropic abnormalities in plant growth. Taken together, these results strongly suggest that OsNMD3 is important for ribosome assembly and the maintenance of normal protein synthesis efficiency.
摘要:
暂无翻译
公众号