An interplay between bZIP16, bZIP68, and GBF1 regulates nuclear photosynthetic genes during photomorphogenesis in ArabidopsisShow others and affiliations
2023 (English)In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 240, no 3, p. 1082-1096Article in journal (Refereed) Published
Abstract [en]
The development of a seedling into a photosynthetically active plant is a crucial process. Despite its importance, we do not fully understand the regulatory mechanisms behind the establishment of functional chloroplasts. We herein provide new insight into the early light response by identifying the function of three basic region/leucine zipper (bZIP) transcription factors: bZIP16, bZIP68, and GBF1. These proteins are involved in the regulation of key components required for the establishment of photosynthetically active chloroplasts. The activity of these bZIPs is dependent on the redox status of a conserved cysteine residue, which provides a mechanism to finetune light-responsive gene expression. The blue light cryptochrome (CRY) photoreceptors provide one of the major light-signaling pathways, and bZIP target genes overlap with one-third of CRY-regulated genes with an enrichment for photosynthesis/chloroplast-associated genes. bZIP16, bZIP68, and GBF1 were demonstrated as novel interaction partners of CRY1. The interaction between CRY1 and bZIP16 was stimulated by blue light. Furthermore, we demonstrate a genetic link between the bZIP proteins and cryptochromes as the cry1cry2 mutant is epistatic to the cry1cry2bzip16bzip68gbf1 mutant. bZIP16, bZIP68, and GBF1 regulate a subset of photosynthesis associated genes in response to blue light critical for a proper greening process in Arabidopsis.
Place, publisher, year, edition, pages
John Wiley & Sons, 2023. Vol. 240, no 3, p. 1082-1096
Keywords [en]
Arabidopsis thaliana, bZIP, chloroplast development, cryptochrome, light signaling, photomorphogenesis
National Category
Forest Science Genetics and Genomics
Identifiers
URN: urn:nbn:se:umu:diva-214055DOI: 10.1111/nph.19219ISI: 001052240200001PubMedID: 37602940Scopus ID: 2-s2.0-85168572043OAI: oai:DiVA.org:umu-214055DiVA, id: diva2:1794572
Funder
Swedish Research CouncilNIH (National Institutes of Health), R35GM1250032023-09-062023-09-062025-02-01Bibliographically approved