Overexpression of the transcription factor ANAC017 results in a genomes uncoupled phenotype under lincomycin

Abstract

SUMMARYOver‐expression (OE) lines for the ER‐tethered NAC transcription factor ANAC017 displayed de‐repression of gun marker genes when grown on lincomycin (lin). RNA‐seq revealed that ANAC017OE2 plants constitutively expressed greater than 40% of the genes induced in wild‐type with lin treatment, including plastid encoded genes ycf1.2 and the gene cluster ndhH‐ndhA‐ndhI‐ndhG‐ndhE‐psaC‐ndhD, documented as direct RNA targets of GUN1. Genes encoding components involved in organelle translation were enriched in constitutively expressed genes in ANAC017OE2. ANAC017OE resulted in constitutive location in the nucleus and significant constitutive binding of ANAC017 was detected by ChIP‐Seq to target genes. ANAC017OE2 lines maintained the ability to green on lin, were more ABA sensitive, did not show photo‐oxidative damage after exposure of de‐etiolated seedlings to continuous light and the transcriptome response to lin were as much as 80% unique compared to gun1‐1. Both double mutants, gun1‐1:ANAC017OE and bzip60:ANAC017OE (but not single bzip60), have a gun molecular gene expression pattern and result in variegated and green plants, suggesting that ANAC017OE may act through an independent pathway compared to gun1. Over‐expression of ANAC013 or rcd1 did not produce a GUN phenotype or green plants on lin. Thus, constitutive ANAC017OE2 establishes an alternative transcriptional program that likely acts through a number of pathways, that is, maintains plastid gene expression, and induction of a variety of transcription factors involved in reactive oxygen species metabolism, priming plants for lin tolerance to give a gun phenotype.