tpj12011-sup-0001-FigureS1.epsimage/eps649KFigure S1. Plastid transcription is required for PhANG expression in Arabidopsis.
tpj12011-sup-0002-FigureS2.epsimage/eps5934KFigure S2. SIG2 and SIG6-mediated plastid transcription is required for PhANG expression.
tpj12011-sup-0003-FigureS3.epsimage/eps6955KFigure S3. Genetic interaction between sigma and gun mutants.
tpj12011-sup-0004-FigureS4.epsimage/eps3301KFigure S4. Correlation of PhANG and plastid gene expression in sig2 and sig6.
tpj12011-sup-0005-FigureS5.epsimage/eps3209KFigure S5. SIG2 and SIG6 are partially redundant for genome coordination.
tpj12011-sup-0006-FigureS6.epsimage/eps5369KFigure S6. The gun1 mutation further reduces plastid transcripts in sig6 mutants.
tpj12011-sup-0007-FigureS7.epsimage/eps1287KFigure S7. Analysis of glutamyl-tRNA levels in sig2 and sig6 mutants.
tpj12011-sup-0008-FigureS8.epsimage/eps4293KFigure S8. SIG2-mediated signals involve tetrapyrrole synthesis.
tpj12011-sup-0009-FigureS9.epsimage/eps686KFigure S9. NF reduces plastid gene expression.
tpj12011-sup-0010-FigureS10.epsimage/eps1112KFigure S10. Microarray analysis of sigma mutants and drug inhibitor treatments.
tpj12011-sup-0011-TableS1.docxWord document76KTable S1. Arabidopsis mutants used in study.
tpj12011-sup-0012-TableS2.docxWord document51KTable S2. List of control genes used in this study.
tpj12011-sup-0013-TableS3.docxWord document90KTable S3. Primers used in study.
tpj12011-sup-0014-TableS4.docxWord document75KTable S4. Plasmids used in study.
tpj12011-sup-0015-TableS5.docxWord document49KTable S5. Overlap of retrograde-responsive nuclear genes identified by microarray analysis
tpj12011-sup-0016-TableS6.xlsxapplication/msexcel251KTable S6. List of genes up-regulated by retrograde signals as identified by microarray analysis.
tpj12011-sup-0017-TableS7.xlsxapplication/msexcel371KTable S7. List of genes down-regulated by retrograde signals as identified by microarray analysis.
tpj12011-sup-0018-MethodsS1.docxapplication/msexcel33KMethods S1. Supplemental experimental procedures: construction of overexpression plasmids; protein extraction and Western Blot analysis; microarray expression and cluster analysis.

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