4.7 Article

Chromatin Changes in Phytochrome Interacting Factor-Regulated Genes Parallel Their Rapid Transcriptional Response to Light

Journal

FRONTIERS IN PLANT SCIENCE
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2022.803441

Keywords

photomorphogenesis; histone acetylation; transcriptional regulation; phytochrome interacting factor (PIF); chromatin modification and gene reprogramming

Categories

Funding

  1. NIH [5R01GM04747524]
  2. US Department of Agriculture Agricultural Research Service Current Research Information System Grant [2030-21000051-00D]
  3. EMBO LongTerm Fellowship [ALTF 385-2016]
  4. Burroughs Wellcome Fund Career Award at the Scientific Interface
  5. Sloan Research Foundation
  6. Human Frontier Science Program
  7. Searle Scholars Program
  8. Shurl and Kay Curci Foundation
  9. Hellman Foundation
  10. NIH Director's New Innovator Award [DP2 OD024541-01]
  11. NSF CAREER Award [1652236]

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This study identifies rapidly light-responsive genes and their relationship with chromatin modifications, suggesting that light-induced transcriptional and chromatin-remodeling processes may be mechanistically intertwined.
As sessile organisms, plants must adapt to a changing environment, sensing variations in resource availability and modifying their development in response. Light is one of the most important resources for plants, and its perception by sensory photoreceptors (e.g., phytochromes) and subsequent transduction into long-term transcriptional reprogramming have been well characterized. Chromatin changes have been shown to be involved in photomorphogenesis. However, the initial short-term transcriptional changes produced by light and what factors enable these rapid changes are not well studied. Here, we define rapidly light-responsive, Phytochrome Interacting Factor (PIF) direct-target genes (LRP-DTGs). We found that a majority of these genes also show rapid changes in Histone 3 Lysine-9 acetylation (H3K9ac) in response to the light signal. Detailed time-course analysis of transcript and chromatin changes showed that, for light-repressed genes, H3K9 deacetylation parallels light-triggered transcriptional repression, while for light-induced genes, H3K9 acetylation appeared to somewhat precede light-activated transcript accumulation. However, direct, real-time imaging of transcript elongation in the nucleus revealed that, in fact, transcriptional induction actually parallels H3K9 acetylation. Collectively, the data raise the possibility that light-induced transcriptional and chromatin-remodeling processes are mechanistically intertwined. Histone modifying proteins involved in long term light responses do not seem to have a role in this fast response, indicating that different factors might act at different stages of the light response. This work not only advances our understanding of plant responses to light, but also unveils a system in which rapid chromatin changes in reaction to an external signal can be studied under natural conditions.

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