Phytochrome interacting factors 4 and 5 redundantly limit seedling de-etiolation in continuous far-red light

Autor: Christian Fankhauser, Séverine Lorrain, Martine Trevisan, Sylvain Pradervand
Jazyk: angličtina
Rok vydání: 2009
Předmět:
0106 biological sciences
Light
Phytochrome A/genetics
Mutant
Arabidopsis
Plant Science
Seedlings/genetics
Arabidopsis/metabolism
01 natural sciences
03 medical and health sciences
Phytochrome A
Gene Expression Regulation
Plant

Botany
Arabidopsis/growth & development
Phytochrome A/metabolism
Genetics
Basic Helix-Loop-Helix Transcription Factors
Arabidopsis/genetics
phytochrome
phytochrome A (phyA)
phytochrome interacting factor (PIF)
photomorphogenesis
priming
Transcription factor
030304 developmental biology
Basic Helix-Loop-Helix Transcription Factors/metabolism
Oligonucleotide Array Sequence Analysis
0303 health sciences
Seedlings/growth & development
Phytochrome
biology
Basic Helix-Loop-Helix Transcription Factors/genetics
Arabidopsis Proteins
Far-red
Seedlings/radiation effects
Cell Biology
biology.organism_classification
Cell biology
Arabidopsis Proteins/genetics
Seedlings
Seedlings/metabolism
Etiolation
Mutation
Arabidopsis Proteins/metabolism
Arabidopsis/radiation effects
Photomorphogenesis
010606 plant biology & botany
Zdroj: The Plant Journal, vol. 60, no. 3, pp. 449-461
The Plant journal : for cell and molecular biology
Popis: Phytochromes are red/far-red photosensors that regulate numerous developmental programs in plants. Among them, phytochrome A (phyA) is essential to enable seedling de-etiolation under continuous far-red (FR) light, a condition that mimics the environment under a dense canopy. The ecological relevance of this response is demonstrated by the high mortality rate of phyA mutant plants that germinate in deep vegetational shade. phyA signaling involves direct interaction of the photoreceptor with phytochrome-interacting factors PIF1 and PIF3, members of the bHLH transcription factor family. Here we investigated the involvement of PIF4 and PIF5 in phyA signaling, and found that they redundantly control de-etiolation in FR light. The pif4 pif5 double mutant is hypersensitive to low fluence rates of FR light. This phenotype is dependent on FR light perception by phyA, but does not rely on alterations in the phyA level. Our microarray analysis shows that PIF4 and PIF5 are part of an inhibitory mechanism that represses the expression of some light-responsive genes in the dark, and that they are also needed for full expression of several growth-related genes in the light. Unlike PIF1 and PIF3, PIF4 and PIF5 are not degraded in response to FR light, indicating that they are light-regulated by a different mechanism. Our genetic analysis suggests that this is achieved through sequestration of these PIFs by the closely related bHLH transcription factor HFR1 (long hypocotyl in FR light).
Databáze: OpenAIRE