A single nucleotide mutation of IspF gene involved in the MEP pathway for isoprenoid biosynthesis causes yellow-green leaf phenotype in rice
Key message We identified IspF gene through yellow-green leaf mutant 505ys in rice. OsIspF was expressed in all tissues detected, and its encoded protein was targeted to the chloroplast. On expression levels of genes in this mutant, OsIspF itself and the genes encoding other enzymes of the MEP pathw...
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Veröffentlicht in: | Plant molecular biology 2018, Vol.96 (1-2), p.5-16 |
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Sprache: | eng |
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We identified
IspF
gene through yellow-green leaf mutant
505ys
in rice.
OsIspF
was expressed in all tissues detected, and its encoded protein was targeted to the chloroplast. On expression levels of genes in this mutant,
OsIspF
itself and the genes encoding other enzymes of the MEP pathway and chlorophyll synthase were all up-regulated, however, among eight genes associated with photosynthesis, only
psaA
,
psaN
and
psbA
genes for three reaction center subunits of photosystem obviously changed.
Isoprenoids are the most abundant natural compounds in all organisms, which originate from the basic five-carbon units isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). In plants, IPP and DMAPP are synthesized through two independent pathways, the mevalonic acid pathway in cytoplasm and the 2-
C
-methyl-
d
-erythritol 4-phosphate (MEP) pathway in plastids. The MEP pathway comprises seven enzymatic steps, in which IspF is the fifth enzyme. So far, no
IspF
gene has been identified in monocotyledonous plants. In this study, we isolated a leaf-color mutant,
505ys
, in rice (
Oryza sativa
). The mutant displayed yellow-green leaf phenotype, reduced level of photosynthetic pigments, and arrested development of chloroplasts. By map-based cloning of this mutant, we identified
OsIspF
gene (
LOC_Os02g45660
) showing significant similarity to
IspF
gene of
Arabidopsis
, in which a missense mutation occurred in the mutant, resulting in an amino acid change in the encoded protein.
OsIspF
gene was expressed in all tissues detected, and its encoded protein was targeted to the chloroplast. Further, the mutant phenotype of
505ys
was complemented by transformation with the wild-type
OsIspF
gene. Therefore, we successfully identified an
IspF
gene in monocotyledonous plants. In addition, real-time quantitative RT-PCR implied that a positive regulation could exist between the
OsIspF
gene and the genes encoding other enzymes of the MEP pathway and chlorophyll synthase. At the same time, it also implied that the individual genes involved in the MEP pathway might differentially regulated expression levels of the genes associated with photosynthesis. |
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ISSN: | 0167-4412 1573-5028 |
DOI: | 10.1007/s11103-017-0668-7 |