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1.
Rice (N Y) ; 11(1): 58, 2018 Oct 11.
Article in English | MEDLINE | ID: mdl-30311098

ABSTRACT

BACKGROUND: The pollen wall, which protects male gametophyte against various stresses and facilitates pollination, is essential for successful reproduction in flowering plants. The pollen wall consists of gametophyte-derived intine and sporophyte-derived exine. From outside to inside of exine are tectum, bacula, nexine I and nexine II layers. How these structural layers are formed has been under extensive studies, but the molecular mechanisms remain obscure. RESULTS: Here we identified two osabcg3 allelic mutants and demonstrated that OsABCG3 was required for pollen development in rice. OsABCG3 encodes a half-size ABCG transporter localized on the plasma membrane. It was mainly expressed in anther when exine started to form. Loss-function of OsABCG3 caused abnormal degradation of the tapetum. The mutant pollen lacked the nexine II and intine layers, and shriveled without cytoplasm. The expression of some genes required for pollen wall formation was examined in osabcg3 mutants. The mutation did not alter the expression of the regulatory genes and lipid metabolism genes, but altered the expression of lipid transport genes. CONCLUSIONS: Base on the genetic and cytological analyses, OsABCG3 was proposed to transport the tapetum-produced materials essential for pollen wall formation. This study provided a new perspective to the genetic regulation of pollen wall development.

2.
Plant Cell Physiol ; 57(4): 798-812, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26872834

ABSTRACT

Flowering time, or heading date, is a critical agronomic trait that determines the cropping season and regional adaptability, and ultimately grain yield in rice. A number of genes involved in photoperiodic flowering have been cloned and their roles in modulating expression of the flowering genes have been characterized to a certain extent. However, much less is known about the pathway in transmitting the day length response signal(s) to induce transition to reproductive growth. Here, we report a constitutive flowering repressor OsCOL10, which encodes a member of the CONSTANS-like (COL) family. Transgenic rice plants overexpressing OsCOL10 (driven by a strong promoter or by fusing it to the activation domain of VP64) showed delayed flowering time under both short and long days.OsCOL10 is affected by the circadian clock and is preferentially expressed in leaf mesophyll cells; it is localized to the nucleus and has transcriptional activation activity. Further studies show that OsCOL10 represses the expression of theFT-like genes RFT1 and Hd3a through Ehd1. Transcripts of OsCOL10 are more abundant in plants carrying a functional Ghd7 allele or overexpressing Ghd7 than in Ghd7-deficient plants, thus placing OsCOL10 downstream of Ghd7.Taking these findings together, we conclude that OsCOL10 functions as a flowering time repressor that links Ghd7 and Ehd1 in rice.


Subject(s)
Flowers/genetics , Gene Expression Regulation, Plant , Oryza/physiology , Plant Proteins/genetics , Cell Nucleus/metabolism , Circadian Clocks/genetics , Mesophyll Cells/physiology , Oryza/genetics , Photoperiod , Plant Leaves/cytology , Plant Leaves/physiology , Plant Proteins/metabolism , Plants, Genetically Modified
3.
Plant J ; 83(3): 427-38, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26043067

ABSTRACT

Plant breeding relies on creation of novel allelic combinations for desired traits. Identification and utilization of beneficial alleles, rare alleles and evolutionarily conserved genes in the germplasm (referred to as 'hidden' genes) provide an effective approach to achieve this goal. Here we show that a chemically induced null mutation in an evolutionarily conserved gene, FUWA, alters multiple important agronomic traits in rice, including panicle architecture, grain shape and grain weight. FUWA encodes an NHL domain-containing protein, with preferential expression in the root meristem, shoot apical meristem and inflorescences, where it restricts excessive cell division. Sequence analysis revealed that FUWA has undergone a bottleneck effect, and become fixed in landraces and modern cultivars during domestication and breeding. We further confirm a highly conserved role of FUWA homologs in determining panicle architecture and grain development in rice, maize and sorghum through genetic transformation. Strikingly, knockdown of the FUWA transcription level by RNA interference results in an erect panicle and increased grain size in both indica and japonica genetic backgrounds. This study illustrates an approach to create new germplasm with improved agronomic traits for crop breeding by tapping into evolutionary conserved genes.


Subject(s)
Gene Expression Regulation, Plant , Genes, Plant , Germ-Line Mutation , Oryza/growth & development , Oryza/genetics , Plant Proteins/genetics , Molecular Sequence Data , Sorghum/growth & development , Zea mays/growth & development
4.
Proc Natl Acad Sci U S A ; 111(46): 16337-42, 2014 Nov 18.
Article in English | MEDLINE | ID: mdl-25378698

ABSTRACT

Success of modern agriculture relies heavily on breeding of crops with maximal regional adaptability and yield potentials. A major limiting factor for crop cultivation is their flowering time, which is strongly regulated by day length (photoperiod) and temperature. Here we report identification and characterization of Days to heading 7 (DTH7), a major genetic locus underlying photoperiod sensitivity and grain yield in rice. Map-based cloning reveals that DTH7 encodes a pseudo-response regulator protein and its expression is regulated by photoperiod. We show that in long days DTH7 acts downstream of the photoreceptor phytochrome B to repress the expression of Ehd1, an up-regulator of the "florigen" genes (Hd3a and RFT1), leading to delayed flowering. Further, we find that haplotype combinations of DTH7 with Grain number, plant height, and heading date 7 (Ghd7) and DTH8 correlate well with the heading date and grain yield of rice under different photoperiod conditions. Our data provide not only a macroscopic view of the genetic control of photoperiod sensitivity in rice but also a foundation for breeding of rice cultivars better adapted to the target environments using rational design.


Subject(s)
Genes, Plant , Oryza/genetics , Photoperiod , Plant Proteins/physiology , Quantitative Trait Loci , Adaptation, Physiological , Agrobacterium tumefaciens/genetics , Biomass , Cloning, Molecular , Crosses, Genetic , Gene Expression Regulation, Plant , Genetic Vectors/genetics , Haplotypes/genetics , Oryza/growth & development , Oryza/radiation effects , Plant Growth Regulators/genetics , Plant Proteins/genetics , Recombinant Fusion Proteins/metabolism , Time Factors
5.
Plant Cell Rep ; 33(9): 1581-94, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24917171

ABSTRACT

KEY MESSAGE: Mutation of the AM1 gene causes an albino midrib phenotype and enhances tolerance to drought in rice K(+) efflux antiporter (KEA) genes encode putative potassium efflux antiporters that are mainly located in plastid-containing organisms, ranging from lower green algae to higher flowering plants. However, little genetic evidence has been provided on the functions of KEA in chloroplast development. In this study, we isolated a rice mutant, albino midrib 1 (am1), with green- and white-variegation in the first few leaves, and albino midrib phenotype in older tissues. We found that AM1 encoded a putative KEA in chloroplast. AM1 was highly expressed in leaves, while lowly in roots. Chloroplast gene expression and proteins accumulation were affected during chlorophyll biosynthesis and photosynthesis in am1 mutants. Interestingly, AM1 was induced by salt and PEG, and am1 showed enhanced sensitivity to salinity in seed germination and increased tolerance to drought. Taken together, we concluded that KEAs were involved in chloroplast development and played important roles in drought tolerance.


Subject(s)
Antiporters/genetics , Chloroplasts/physiology , Gene Expression Regulation, Plant , Oryza/genetics , Potassium/metabolism , Amino Acid Sequence , Antiporters/metabolism , Chlorophyll/metabolism , Droughts , Germination , Molecular Sequence Data , Mutation , Oryza/physiology , Oryza/ultrastructure , Phenotype , Photosynthesis , Phylogeny , Plant Leaves/genetics , Plant Leaves/physiology , Plant Leaves/ultrastructure , Plant Proteins/genetics , Plant Proteins/metabolism , Plants, Genetically Modified , Recombinant Fusion Proteins , Salinity , Seedlings/genetics , Seedlings/physiology , Seedlings/ultrastructure , Seeds/genetics , Seeds/physiology , Seeds/ultrastructure , Sequence Alignment
6.
Plant J ; 78(3): 468-80, 2014 May.
Article in English | MEDLINE | ID: mdl-24635058

ABSTRACT

Low temperature (LT) is one of the most prevalent factors limiting the productivity and geographical distribution of rice (Oryza sativa L.). Although significant progress has been made in elucidating the effect of LT on seed germination and reproductive development in rice, the genetic component affecting vegetative growth under LT remains poorly understood. Here, we report that rice cultivars harboring the dominant LTG1 (Low Temperature Growth 1) allele are more tolerant to LT (15-25°C, a temperature range prevalent in high-altitude, temperate zones and high-latitude areas), than those with the ltg1 allele. Using a map-based cloning strategy, we show that LTG1 encodes a casein kinase I. A functional nucleotide polymorphism was identified in the coding region of LTG1, causing a single amino acid substitution (I357K) that is associated with the growth rate, heading date and yield of rice plants grown at LT. We present evidence that LTG1 affects rice growth at LT via an auxin-dependent process(es). Furthermore, phylogenetic analysis of this locus suggests that the ltg1 haplotype arose before the domestication of rice in tropical climates. Together, our data demonstrate that LTG1 plays an important role in the adaptive growth and fitness of rice cultivars under conditions of low ambient temperature.


Subject(s)
Adaptation, Physiological , Oryza/physiology , Plant Proteins/metabolism , Alleles , Amino Acid Substitution , Casein Kinase I/genetics , Casein Kinase I/metabolism , Cloning, Molecular , Cold Temperature , Gene Expression Regulation, Plant , Haplotypes , Indoleacetic Acids/metabolism , Oryza/genetics , Oryza/growth & development , Phylogeny , Plant Proteins/genetics , Plants, Genetically Modified , Polymorphism, Genetic
7.
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
8.
Plant J ; 64(5): 812-24, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21105928

ABSTRACT

Rice glutelins are synthesized at the endoplasmic reticulum (ER) as precursors (pro-glutelins), and are transported to protein storage vacuoles, where they are processed into mature proteins. The molecular basis of this process is largely unknown. Here, we report the isolation of a rice mutant, gpa1, that accumulates 57 kDa pro-glutelins in seeds and whose endosperm has a floury appearance. Transmission electron microscopy analysis showed that the gpa1 endosperm cells have an enlarged ER lumen and a smaller protein body II (PBII), and accumulated three types of newly generated subcellular structures. Moreover, a proportion of glutelins in the gpa1 endosperm cells were not delivered to PBII, and instead were mis-targeted to two of the newly generated structures or secreted. The gene corresponding to the gpa1 mutation was found to be OsRab5a, which encodes a small GTPase. In Arabidopsis protoplasts, OsRab5a protein was found to co-localize predominantly with AtVSR2, a molecular marker for the pre-vacuolar compartments (PVC). We conclude that OsRab5a plays an essential role in trafficking of storage protein to PBII, possibly as part of its function in organizing the endomembrane system in developing endosperm cells of rice.


Subject(s)
Endosperm/metabolism , Glutens/metabolism , Oryza/genetics , Plant Proteins/metabolism , rab5 GTP-Binding Proteins/metabolism , Chromosome Mapping , Endosperm/ultrastructure , Genetic Complementation Test , Microscopy, Electron, Transmission , Mutation , Oryza/metabolism , Plant Proteins/genetics , Plants, Genetically Modified/genetics , Plants, Genetically Modified/metabolism , Protein Transport , RNA, Plant/genetics , Seed Storage Proteins/metabolism , Vacuoles/metabolism , Vacuoles/ultrastructure , rab5 GTP-Binding Proteins/genetics
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