Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Plant Physiol ; 162(4): 1867-80, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23803583

ABSTRACT

The plastidic caseinolytic protease (Clp) of higher plants is an evolutionarily conserved protein degradation apparatus composed of a proteolytic core complex (the P and R rings) and a set of accessory proteins (ClpT, ClpC, and ClpS). The role and molecular composition of Clps in higher plants has just begun to be unraveled, mostly from studies with the model dicotyledonous plant Arabidopsis (Arabidopsis thaliana). In this work, we isolated a virescent yellow leaf (vyl) mutant in rice (Oryza sativa), which produces chlorotic leaves throughout the entire growth period. The young chlorotic leaves turn green in later developmental stages, accompanied by alterations in chlorophyll accumulation, chloroplast ultrastructure, and the expression of chloroplast development- and photosynthesis-related genes. Positional cloning revealed that the VYL gene encodes a protein homologous to the Arabidopsis ClpP6 subunit and that it is targeted to the chloroplast. VYL expression is constitutive in most tissues examined but most abundant in leaf sections containing chloroplasts in early stages of development. The mutation in vyl causes premature termination of the predicted gene product and loss of the conserved catalytic triad (serine-histidine-aspartate) and the polypeptide-binding site of VYL. Using a tandem affinity purification approach and mass spectrometry analysis, we identified OsClpP4 as a VYL-associated protein in vivo. In addition, yeast two-hybrid assays demonstrated that VYL directly interacts with OsClpP3 and OsClpP4. Furthermore, we found that OsClpP3 directly interacts with OsClpT, that OsClpP4 directly interacts with OsClpP5 and OsClpT, and that both OsClpP4 and OsClpT can homodimerize. Together, our data provide new insights into the function, assembly, and regulation of Clps in higher plants.


Subject(s)
Endopeptidase Clp/genetics , Oryza/genetics , Plant Leaves/genetics , Plant Proteins/genetics , Plastids/enzymology , Binding Sites , Chlorophyll/genetics , Chlorophyll/metabolism , Chloroplasts/genetics , Cloning, Molecular , Endopeptidase Clp/metabolism , Gene Expression Regulation, Plant , Oryza/metabolism , Phenotype , Photosynthesis/genetics , Plant Proteins/metabolism , Plants, Genetically Modified , Plastids/genetics , Plastids/metabolism , Protein Interaction Mapping , Two-Hybrid System Techniques
2.
PLoS Genet ; 9(2): e1003281, 2013.
Article in English | MEDLINE | ID: mdl-23437005

ABSTRACT

Land plants have evolved increasingly complex regulatory modes of their flowering time (or heading date in crops). Rice (Oryza sativa L.) is a short-day plant that flowers more rapidly in short-day but delays under long-day conditions. Previous studies have shown that the CO-FT module initially identified in long-day plants (Arabidopsis) is evolutionary conserved in short-day plants (Hd1-Hd3a in rice). However, in rice, there is a unique Ehd1-dependent flowering pathway that is Hd1-independent. Here, we report isolation and characterization of a positive regulator of Ehd1, Early heading date 4 (Ehd4). ehd4 mutants showed a never flowering phenotype under natural long-day conditions. Map-based cloning revealed that Ehd4 encodes a novel CCCH-type zinc finger protein, which is localized to the nucleus and is able to bind to nucleic acids in vitro and transactivate transcription in yeast, suggesting that it likely functions as a transcriptional regulator. Ehd4 expression is most active in young leaves with a diurnal expression pattern similar to that of Ehd1 under both short-day and long-day conditions. We show that Ehd4 up-regulates the expression of the "florigen" genes Hd3a and RFT1 through Ehd1, but it acts independently of other known Ehd1 regulators. Strikingly, Ehd4 is highly conserved in the Oryza genus including wild and cultivated rice, but has no homologs in other species, suggesting that Ehd4 is originated along with the diversification of the Oryza genus from the grass family during evolution. We conclude that Ehd4 is a novel Oryza-genus-specific regulator of Ehd1, and it plays an essential role in photoperiodic control of flowering time in rice.


Subject(s)
Flowers , Nuclear Proteins/genetics , Oryza , Photoperiod , Plant Proteins , Trans-Activators/genetics , Arabidopsis/genetics , Arabidopsis/metabolism , Flowers/genetics , Flowers/growth & development , Gene Expression Regulation, Plant , Oryza/genetics , Oryza/growth & development , Phenotype , Plant Leaves/genetics , Plant Leaves/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism
3.
Plant Physiol ; 159(1): 227-38, 2012 May.
Article in English | MEDLINE | ID: mdl-22430843

ABSTRACT

The pentatricopeptide repeat (PPR) gene family represents one of the largest gene families in higher plants. Accumulating data suggest that PPR proteins play a central and broad role in modulating the expression of organellar genes in plants. Here we report a rice (Oryza sativa) mutant named young seedling albino (ysa) derived from the rice thermo/photoperiod-sensitive genic male-sterile line Pei'ai64S, which is a leading male-sterile line for commercial two-line hybrid rice production. The ysa mutant develops albino leaves before the three-leaf stage, but the mutant gradually turns green and recovers to normal green at the six-leaf stage. Further investigation showed that the change in leaf color in ysa mutant is associated with changes in chlorophyll content and chloroplast development. Map-based cloning revealed that YSA encodes a PPR protein with 16 tandem PPR motifs. YSA is highly expressed in young leaves and stems, and its expression level is regulated by light. We showed that the ysa mutation has no apparent negative effects on several important agronomic traits, such as fertility, stigma extrusion rate, selfed seed-setting rate, hybrid seed-setting rate, and yield heterosis under normal growth conditions. We further demonstrated that ysa can be used as an early marker for efficient identification and elimination of false hybrids in commercial hybrid rice production, resulting in yield increases by up to approximately 537 kg ha(-1).


Subject(s)
Oryza/metabolism , Phenotype , Plant Proteins/genetics , Seedlings/metabolism , Seeds/metabolism , Amino Acid Motifs , Amino Acid Sequence , Biomarkers , Chimera/genetics , Chimera/metabolism , Chlorophyll/metabolism , Chloroplasts/metabolism , Chloroplasts/ultrastructure , Chromosome Mapping , Chromosomes, Plant/genetics , Chromosomes, Plant/metabolism , Cloning, Molecular , Crosses, Genetic , Fertility , Genes, Plant , Hybrid Vigor , Microscopy, Electron, Transmission , Molecular Sequence Data , Mutation , Oryza/anatomy & histology , Oryza/genetics , Photoperiod , Plant Leaves/anatomy & histology , Plant Leaves/metabolism , Plant Proteins/metabolism , Plant Stems/metabolism , Plant Stems/physiology , Plants, Genetically Modified/genetics , Plants, Genetically Modified/metabolism , Seedlings/genetics , Seeds/genetics , Transcription, Genetic
SELECTION OF CITATIONS
SEARCH DETAIL
...