Single base substitution in Os CDC48 is responsible for premature senescence and death phenotype in

来源 :Journal of Integrative Plant Biology | 被引量 : 0次 | 上传用户:victor9808
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A premature senescence and death 128(psd128)mutant was isolated from an ethyl methane sulfonate-induced rice IR64 mutant bank. The premature senescence phenotype appeared at the six-leaf stage and the plant died at the early heading stage. psd128 exhibited impaired chloroplast development with significantly reduced photosynthetic ability,chlorophyll and carotenoid contents, root vigor, soluble protein content and increased malonaldehyde content.Furthermore, the expression of senescence-related genes was significantly altered in psd128. The mutant trait was controlled by a single recessive nuclear gene. Using mapbased strategy, the mutation Oryza sativa cell division cycle 48(Os CDC48) was isolated and predicted to encode a putative AAA-type ATPase with 809 amino-acid residuals. A single base substitution at position C2347 T in psd128 resulted in a premature stop codon. Functional complementation could rescue the mutant phenotype. In addition, RNA interference resulted in the premature senescence and death phenotype.Os CDC48 was expressed constitutively in the root, stem, leaf and panicle. Subcellular analysis indicated that Os CDC48:YFP fusion proteins were located both in the cytoplasm and nucleus. Os CDC48 was highly conserved with more than 90%identity in the protein levels among plant species. Our results indicated that the impaired function of Os CDC48 was responsible for the premature senescence and death phenotype. A premature senescence and death 128 (psd128) mutant was isolated from an ethyl methane sulfonate-induced rice IR64 mutant bank. The premature senescence phenotype was at the six-leaf stage and the plant died at the early heading stage. Psd128 discover impaired chloroplast development The significantly reduced photosynthetic ability, chlorophyll and carotenoid contents, root vigor, soluble protein content and increased malonaldehyde content. Still further, the expression of senescence-related genes was significantly altered in psd128. The mutant trait was controlled by a single recessive nuclear gene. mapbased strategy, the mutation Oryza sativa cell division cycle 48 (Os CDC48) was isolated and predicted to encode a putative AAA-type ATPase with 809 amino-acid residuals. A single base substitution at position C2347 T in psd128 resulted in a premature stop codon Functional complementation could rescue the mutant phenotype. In addition, RNA interference resulted in the premature senescence and death phenotype. Os CDC48 was expressed constitutively in the root, stem, leaf and panicle. Subcellular analysis indicated that Os CDC48: YFP fusion proteins were located both in the cytoplasm and nucleus. Os CDC48 was highly conserved with more than 90% identity in the protein levels among plant species. Our results indicated that the impaired function of Os CDC48 was responsible for the premature senescence and death phenotype.
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