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Hydrogen sulfide promotes flowering in heading Chinese cabbage by S-sulfhydration of BraFLCs

Heading Chinese cabbage (Brassica rapa L. syn. B. campestris L. ssp. chinensis Makino var. pekinensis (Rupr.) J. Cao et Sh. Cao) is a cruciferous Brassica vegetable that has a triplicate genome, owing to an ancient genome duplication event. It is unclear whether the duplicated homologs have conserve...

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Detalles Bibliográficos
Autores principales: Ma, Xiaoli, Zhang, Liping, Pei, Zhuoya, Zhang, Linlin, Liu, Zhiqiang, Liu, Danmei, Hao, Xuefeng, Jin, Zhuping, Pei, Yanxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848000/
https://www.ncbi.nlm.nih.gov/pubmed/33518701
http://dx.doi.org/10.1038/s41438-020-00453-3
Descripción
Sumario:Heading Chinese cabbage (Brassica rapa L. syn. B. campestris L. ssp. chinensis Makino var. pekinensis (Rupr.) J. Cao et Sh. Cao) is a cruciferous Brassica vegetable that has a triplicate genome, owing to an ancient genome duplication event. It is unclear whether the duplicated homologs have conserved or diversified functions. Hydrogen sulfide (H(2)S) is a plant gasotransmitter that plays important physiological roles in growth, development, and responses to environmental stresses. The modification of cysteines through S-sulfhydration is an important mechanism of H(2)S, which regulates protein functions. H(2)S promotes flowering in Arabidopsis and heading Chinese cabbage. Here we investigated the molecular mechanisms of H(2)S used to promote flowering in the latter. Four, five, and four BraFLC, BraSOC I, and BraFT homologs were identified in heading Chinese cabbage. Different BraFLC proteins were bound to different CArG boxes in the promoter regions of the BraSOC I and BraFT homologs, producing different binding patterns. Thus, there may be functionally diverse BraFLC homologs in heading Chinese cabbage. Exogenous H(2)S at 100 μmol L(−1) significantly promoted flowering by compensating for insufficient vernalization. BraFLC 1 and BraFLC 3 underwent S-sulfhydration by H(2)S, after which their abilities to bind most BraSOC I or BraFT promoter probes weakened or even disappeared. These changes in binding ability were consistent with the expression pattern of the BraFT and BraSOC I homologs in seedlings treated with H(2)S. These results indicated that H(2)S signaling regulates flowering time. In summary, H(2)S signaling promoted plant flowering by weakening or eliminating the binding abilities of BraFLCs to downstream promoters through S-sulfhydration.