Difference between revisions of "Os03g0264400"
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===Expression=== | ===Expression=== | ||
| − | + | *The expression level of OASA2 in plants homozygous and heterozygous for modified OASA2 was similar to that of nontransformants, suggesting that OASA2 transcription in GT plants was controlled in the same manner as endogenous OASA2, and that GTcould lead to a lower risk of gene silencing than in conventional overexpression approaches. | |
===Evolution=== | ===Evolution=== | ||
Revision as of 10:25, 31 July 2016
OASA2—an a-subunit of anthranilate synthase that is a key enzyme of tryptophan (Trp)vbiosynthesis in rice (Oryza sativa)
Contents
Annotated Information
Function
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Expression
- The expression level of OASA2 in plants homozygous and heterozygous for modified OASA2 was similar to that of nontransformants, suggesting that OASA2 transcription in GT plants was controlled in the same manner as endogenous OASA2, and that GTcould lead to a lower risk of gene silencing than in conventional overexpression approaches.
Evolution
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Labs working on this gene
- Plant Genome Engineering Research Unit, Agrogenomics Research Center, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305–8602, Japan (H.S., H.O., S.T.);
- RIKEN Plant Science Center,Yokohama, Kanagawa 230–0045, Japan (A.O., F.M., K.S.); Graduate School of Pharmaceutical Sciences, Chiba University, Inage-ku, Chiba 263–8522, Japan (K.S.);
- Kihara Institute of Biological Research, Yokohama City University, Yokohama, Kanagawa 244–0813, Japan (S.T.)
References
- de Pater S, Neuteboom LW, Pinas JE, Hooykaas PJJ, van der Zaal BJ (2009) ZFN-induced mutagenesis and gene-targeting in Arabidopsis through Agrobacterium-mediated floral dip transformation. Plant Biotechnol J 7:821–835