2023
DOI: 10.1093/plphys/kiad296
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Cucumber NUCLEAR FACTOR-YC2/-YC9 target translocon component CsTIC21 in chloroplast photomorphogenesis

Abstract: Light signals promote photomorphogenesis and photosynthesis, allowing plants to establish photoautotrophic growth. Chloroplasts are organelles responsible for photosynthesis in which light energy is converted into chemical energy and stored as organic matter. However, how light regulates chloroplast photomorphogenesis remains unclear. Here, we isolated a cucumber (Cucumis sativus L.) mutant albino seedling (as) from an ethyl methane sulfonate mutagenesis (EMS) library with an albino phenotype. Map-based clonin… Show more

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Cited by 6 publications
(3 citation statements)
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“…Therefore, NtNF-YC3 and NtNF-YC16 may be potential candidate genes for regulating photomorphogenesis. In addition, studies have shown that CsNF-YC2 and CsNF-YC9 were involved in chloroplast photomorphogenesis in cucumber, and a CsNF-YC2/-YC9-CsTIC21 model was proposed 46 .…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Therefore, NtNF-YC3 and NtNF-YC16 may be potential candidate genes for regulating photomorphogenesis. In addition, studies have shown that CsNF-YC2 and CsNF-YC9 were involved in chloroplast photomorphogenesis in cucumber, and a CsNF-YC2/-YC9-CsTIC21 model was proposed 46 .…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, NtNF-YC3 and NtNF-YC16 may be potential candidate genes for regulating photomorphogenesis. In addition, studies have shown that CsNF-YC2 and CsNF-YC9 were involved in chloroplast photomorphogenesis in cucumber, and a CsNF-YC2/-YC9-CsTIC21 model was proposed 46 . Many studies have found that NF-Y transcription factors play an important role in plant growth and development and abiotic stress 13 .…”
Section: Discussionmentioning
confidence: 99%
“…This induces the target mRNA to degrade or change its methylation, which stops the target gene from being translated normally [8]. Using VIGS technology, researchers can quickly figure out the function of a target gene by comparing the number of its downregulated transcripts to changes in the plant's biochemistry and physiology [1][2][3][4][5][6][7][8][9][10][11]. This method does not require stable genetic transformation, and it is easy to use when aiming to study gene functions in a short amount of time and at a low cost [12,13].…”
Section: Introductionmentioning
confidence: 99%