Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| Columbia (Col-0) | Col | Control | Control | No mutant | Normal | Leaf | NA | Sequencing RT-PCR products | 100%, 100% | Complete, | None, None | 37530742 | | SAIL_77_E03 | mef28-1 | A T-DNA insertion | The T-DNA insertions of mef28-1 and mef28-2 are located in the DYW domain and the second PPR motif, respectively. | Homozygous | The two T-DNA lines for the MEF28 gene do not show visible growth and developmental defects under standard growth conditions | Leaf | NA | Sequencing RT-PCR products | 0%, 0% | Unedited, | Absent, Ab | 37530742 | | WiscDsLox461-464F22 | mef28-2 | A T-DNA insertion | The T-DNA insertions of mef28-1 and mef28-2 are located in the DYW domain and the second PPR motif, respectively. | Homozygous | The two T-DNA lines for the MEF28 gene do not show visible growth and developmental defects under standard growth conditions | Leaf | NA | Sequencing RT-PCR products | 0%, 0% | Unedited, | Absent, Ab | 37530742 | | SAIL_77_E03 | mef28-1+35S:MEF28 | Complementation | Plants of the mutant line mef28-1 was transformed by dip inoculation with the respective clones of various protein constructs including the chimeras as described previously (Glass et al. 2015). Transg | Homozygous | Normal | Leaf | NA | Sequencing RT-PCR products | 100%, 100% | Complete, | Restored, | 37530742 |
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