Difference between revisions of "Os06g0102100"
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==Annotated Information== | ==Annotated Information== | ||
| − | [[File:99-Os06g0102100.png|right|thumb| | + | [[File:99-Os06g0102100.png|right|thumb|327px|'''Figure 5.''' ''Analysis of the rice CYP93G2 T-DNA mutant<ref name="ref1" />.'']] |
===Gene Symbol=== | ===Gene Symbol=== | ||
*'''''Os06g0102100''''' '''''<=>''''' '''''OsF2H,F2H''''','''''CYP93G2''''' | *'''''Os06g0102100''''' '''''<=>''''' '''''OsF2H,F2H''''','''''CYP93G2''''' | ||
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* In the acid-hydrolyzed methanolic extracts of '''''CYP93G2''''' mutant leaves, the levels of tricin detected were comparable to those of wild-type samples (Fig. 5C). However, the accumulation of isovitexin was substantially reduced in the mutant plants, suggesting that '''''CYP93G2''''' is required for C-glycosylflavone production in rice. In nonhydrolyzed leaf extracts, a range of potential flavone metabolites were detected in the wild-type samples following HPLC separation, which was monitored at 350 nm (Fig. 5D). | * In the acid-hydrolyzed methanolic extracts of '''''CYP93G2''''' mutant leaves, the levels of tricin detected were comparable to those of wild-type samples (Fig. 5C). However, the accumulation of isovitexin was substantially reduced in the mutant plants, suggesting that '''''CYP93G2''''' is required for C-glycosylflavone production in rice. In nonhydrolyzed leaf extracts, a range of potential flavone metabolites were detected in the wild-type samples following HPLC separation, which was monitored at 350 nm (Fig. 5D). | ||
* On the other hand, the majority of these UV light-absorbing compounds eluted at 15 to 22 min were markedly reduced in absorbance in the mutant chromatogram. | * On the other hand, the majority of these UV light-absorbing compounds eluted at 15 to 22 min were markedly reduced in absorbance in the mutant chromatogram. | ||
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You can also add sub-section(s) at will. | You can also add sub-section(s) at will. | ||
Latest revision as of 07:13, 17 October 2016
The rice Os06g0102100 was reported as CYP93G2 in 2010 [1] by researchers from China.
Contents
Annotated Information
Figure 5. Analysis of the rice CYP93G2 T-DNA mutant[1].
Gene Symbol
- Os06g0102100 <=> OsF2H,F2H,CYP93G2
Function
- Rice CYP93G2 Is a Close Homolog of Sorghum CYP93G3
- CYP93G2 is related to the CYP93B subfamily, which consists of dicot flavone synthase II enzymes.
- CYP93G2 generates 2-hydroxy-flavanones, which are modified by O-glycosylation in transgenic Arabidopsis (Arabidopsis thaliana).
- CYP93G2 is the first enzyme that channels flavanones to C-glycosylflavone biosynthesis in rice.
Expression
- The mutant plants did not show observable differences from the wild-type plants with regard to growth, flowering time, or seed yield.
Both tricin and isovitexin are frequently O-glycosylated (Cavaliere et al., 2005), and the aglycones can be released by acid treatment.
- In the acid-hydrolyzed methanolic extracts of CYP93G2 mutant leaves, the levels of tricin detected were comparable to those of wild-type samples (Fig. 5C). However, the accumulation of isovitexin was substantially reduced in the mutant plants, suggesting that CYP93G2 is required for C-glycosylflavone production in rice. In nonhydrolyzed leaf extracts, a range of potential flavone metabolites were detected in the wild-type samples following HPLC separation, which was monitored at 350 nm (Fig. 5D).
- On the other hand, the majority of these UV light-absorbing compounds eluted at 15 to 22 min were markedly reduced in absorbance in the mutant chromatogram.
You can also add sub-section(s) at will.
Labs working on this gene
- School of Biological Sciences (Y.D., H.C., C.L.) and Department of Chemistry (I.K.C.), The University of Hong Kong, Hong Kong, China
