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| Reference | ||
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| Author | Jin X., Baysal C., Drapal M., Sheng Y., Huang X., He W., Shi L., Capell T., Fraser P.D., Christou P., Zhu C. | |
| Title | The Coordinated Upregulated Expression of Genes Involved in MEP, Chlorophyll, Carotenoid and Tocopherol Pathways, Mirrored the Corresponding Metabolite Contents in Rice Leaves during De-Etiolation. | |
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Abstract: Light is an essential regulator of many developmental processes in higher plants. We investigated the effect of 4-hydroxy-3-methylbut-2-enyl diphosphate reductase 1/2 genes (<i>OsHDR1/2</i>) and isopentenyl diphosphate isomerase 1/2 genes (<i>OsIPPI1/2</i>) on the biosynthesis of chlorophylls, carotenoids, and phytosterols in 14-day-old etiolated rice (<i>Oyza sativa</i> L.) leaves during de-etiolation. However, little is known about the effect of isoprenoid biosynthesis genes on the corresponding metabolites during the de-etiolation of etiolated rice leaves. The results showed that the levels of alpha-tocopherol were significantly increased in de-etiolated rice leaves. Similar to 1-deoxy-D-xylulose-5-phosphate synthase 3 gene (<i>OsDXS3</i>), both <i>OsDXS1</i> and <i>OsDXS2</i> genes encode functional 1-deoxy-D-xylulose-5-phosphate synthase (DXS) activities. Their expression patterns and the synthesis of chlorophyll, carotenoid, and tocopherol metabolites suggested that <i>OsDXS1</i> is responsible for the biosynthesis of plastidial isoprenoids in de-etiolated rice leaves. The expression analysis of isoprenoid biosynthesis genes revealed that the coordinated expression of the MEP (2-C-methyl-D-erythritol 4-phosphate) pathway, chlorophyll, carotenoid, and tocopherol pathway genes mirrored the changes in the levels of the corresponding metabolites during de-etiolation. The underpinning mechanistic basis of coordinated light-upregulated gene expression was elucidated during the de-etiolation process, specifically the role of light-responsive <i>cis</i>-regulatory motifs in the promoter region of these genes. In silico promoter analysis showed that the light-responsive <i>cis</i>-regulatory elements presented in all the promoter regions of each light-upregulated gene, providing an important link between observed phenotype during de-etiolation and the molecular machinery controlling expression of these genes. |
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| Journal | Plants (Basel) | |
| Country | China | |
| Volume | 10(7) | |
| Pages | ||
| Year | 2021 | |
| PubMed ID | 34371659 | |
| PubMed Central ID | 8309317 | |
| DOI | 10.3390/plants10071456 | |
| URL | - | |
| Relation | ||
| Gene | CDS5 CMS DXR DXS1 DXS2 DXS3 FGL GRY340 HDS HGGT HMGRI HMGRII HMGRIII HMGS1 HMGS2 HMGS3 HYD2 IPI LAS1 LCYB LYCE LYL1 MCS MK PDA PMK PORA PSY1 PSY2 VTE1 VTE2 VTE4 YGL1 YGL10 ZDS | |
| INSD | - | |
| Strain | Wild Core Collection | - |
| Induced Mutation Lines(NIG Collection) | - | |
| Sterile Seed Strain | - | |
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Lethal Embryo Mutantion Strain |
- | |
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Stages in Each Organ - Muant Lines (Gene) |
- | |
| Cultivated Varieties(NIG Collection) | - | |
| Stages in Each Organ | - | |
