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1.
Plant Mol Biol ; 103(4-5): 473-487, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32266647

RESUMO

KEY MESSAGE: CHR721 functions as a chromatin remodeler and interacts with a known single-stranded binding protein, OsRPA1a, to regulate both male and female reproductive development in rice. Reproductive development and fertility are important for seed production in rice. Here, we identified a sterile rice mutant, chr721, that exhibited defects in both male and female reproductive development. Approximately 5% of the observed defects in chr721, such as asynchronous dyad division, occurred during anaphase II of meiosis. During the mitotic stage, approximately 80% of uninucleate microspores failed to develop into tricellular pollen, leading to abnormal development. In addition, defects in megaspore development were detected after functional megaspore formation. CHR721, which encodes a nuclear protein belonging to the SNF2 subfamily SMARCAL1, was identified by map-based cloning. CHR721 was expressed in various tissues, especially in spikelets. CHR721 was found to interact with replication protein A (OsRPA1a), which is involved in DNA repair. The expressions of genes involved in DNA repair and cell-cycle checkpoints were consistently upregulated in chr721. Although numerous genes involved in male and female development have been identified, the mode of participation of chromatin-remodeling factors in reproductive development is still not well understood. Our results suggest that CHR721, a novel gene cloned from rice, plays a vital role in both male and female reproductive development.


Assuntos
Proteínas de Ligação a DNA/genética , Regulação da Expressão Gênica de Plantas , Oryza/genética , Proteínas de Plantas/genética , Reprodução/genética , Sementes/genética , Ciclo Celular/genética , Ciclo Celular/fisiologia , Cromossomos de Plantas , Clonagem Molecular , Reparo do DNA , Genes de Plantas/genética , Meiose , Oryza/embriologia , Oryza/crescimento & desenvolvimento , Óvulo Vegetal/citologia , Óvulo Vegetal/genética , Desenvolvimento Vegetal/genética , Desenvolvimento Vegetal/fisiologia , Plantas Geneticamente Modificadas , Pólen/genética , Sementes/citologia , Sementes/crescimento & desenvolvimento
2.
Theor Appl Genet ; 108(7): 1420-5, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-14749846

RESUMO

A plant-transformation-competent binary BAC library was constructed from the genomic DNA of the chromosome 9 monosomic addition line of Beta corolliflora Zoss. in sugar beet ( B. vulgaris. L). This monosomic addition line (designated M14) is characterized by diplosporic reproduction caused by the alien chromosome carrying the gene(s) responsible for diplospory. The library consists of 49,920 clones with an average insert size of 127 kb, representing approximately 7.5 haploid genome equivalents and providing a greater than 99% probability of isolating a single-copy DNA sequence from the library. To develop the scaffold of a physical map for the alien chromosome, B. corolliflora genome-specific dispersed repetitive DNA sequences were used as probes to isolate BAC clones derived from the alien chromosome in the library. A total of 2,365 positive clones were obtained and arrayed into a sublibrary specific for B. corolliflora chromosome 9 (designated bcBAC-IX). The bcBAC-IX sublibrary was further screened with a subtractive cDNA pool generated from the ovules of M14 and the floral buds of B. vulgaris by the suppression subtractive hybridization method. One hundred and three positive binary BACs were obtained, which potentially contain the genes of the alien chromosome specifically expressed during the ovule and embryo development of M14, and may be associated with apomictic reproduction. Thus, these binary BAC clones will be useful for identification of the genes for apomixis by genetic transformation.


Assuntos
Beta vulgaris/genética , Cromossomos de Plantas/genética , Biblioteca Gênica , Agricultura/métodos , Southern Blotting , Cromossomos Artificiais Bacterianos/genética , Cruzamentos Genéticos , DNA Complementar/genética , Eletroforese em Gel de Ágar , Sequências Repetitivas Dispersas/genética , Reprodução/genética
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