tpj12180-sup-0001-FigS1.pdfapplication/PDF184KFigure S1. Subcellular localization of OTP71.
tpj12180-sup-0002-FigS2.pdfapplication/PDF5528KFigure S2. Phenotype of otp72–2.
tpj12180-sup-0003-FigS3.pdfapplication/PDF1137KFigure S3. ccmFN2 is co-transcribed with orf117.
tpj12180-sup-0004-FigS4.pdfapplication/PDF153KFigure S4. RACE otp71-specific transcript.
tpj12180-sup-0005-FigS5.pdfapplication/PDF529KFigure S5. HRM screen of plastid editing sites in otp71 and otp72.
tpj12180-sup-0006-FigS6.pdfapplication/PDF156KFigure S6. Alignment of E and DYW domain sequences of Arabidopsis editing factors.
tpj12180-sup-0007-FigS7.pdfapplication/PDF425KFigure S7. Alignment of the swapping constructs used for the complementation experiments.
tpj12180-sup-0008-FigS8.pdfapplication/PDF241KFigure S8. Transgene expression in clb19, crr4, otp71 and otp72 mutants complemented with various domain-swapping constructs.
tpj12180-sup-0009-FigS9.pdfapplication/PDF424KFigure S9. The effects of swapping the E domains of CRR4, CLB19, OTP71 and OTP72 on RNA editing.
tpj12180-sup-0010-FigS10.epsimage/eps424KFigure S10. Alignment of MEF8 and MEF8S to the sequences around their respective editing sites.
tpj12180-sup-0011-TableS1.xlsapplication/msexcel60KTable S1. Editing sites in Arabidopsis mitochondria.
tpj12180-sup-0012-TableS2.xlsapplication/msexcel52KTable S2. Primers used in this work.

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