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Field-work reveals a novel function for MAX2 in a native tobacco's high-light adaptions.
Li, Suhua; Baldwin, Gundega; Yang, Caiqiong; Lu, Ruirui; Meng, Shuaishuai; Huang, Jianbei; Wang, Ming; Baldwin, Ian T.
Afiliación
  • Li S; Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Key Laboratory of Synthetic Biology, Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.
  • Baldwin G; Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Jena, Germany.
  • Yang C; Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Jena, Germany.
  • Lu R; Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Jena, Germany.
  • Meng S; Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Key Laboratory of Synthetic Biology, Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.
  • Huang J; Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Key Laboratory of Synthetic Biology, Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.
  • Wang M; Department of Biogeochemical Processes, Max Planck Institute for Biogeochemistry, Jena, Germany.
  • Baldwin IT; Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Plant Cell Environ ; 47(1): 230-245, 2024 Jan.
Article en En | MEDLINE | ID: mdl-37750501
ABSTRACT
Laboratory studies have revealed that strigolatone (SL) and karrikin (KAR) signalling mediate responses to abiotic and biotic stresses, and reshape branching architecture that could increase reproductive performance and crop yields. To understand the ecological function of SL and KAR signalling, transgenic lines of wild tobacco Nicotiana attenuata, silenced in SL/KAR biosynthesis/signalling were grown in the glasshouse and in two field plots in the Great Basin Desert in Utah over four field seasons. Of the lines silenced in SL and KAR signalling components (irMAX2, irD14, irKAI2 and irD14 × irKAI2 plants), which exhibited the expected increases in shoot branching, only irMAX2 plants showed a strong leaf-bleaching phenotype when grown in the field. In the field, irMAX2 plants had lower sugar and higher leaf amino acid contents, lower lifetime fitness and were more susceptible to herbivore attack compared to wild-type plants. These irMAX2 phenotypes were not observed in glasshouse-grown plants. Transcriptomic analysis revealed dramatic responses to high-light intensity in irMAX2 leaves in the field lutein contents decreased, and transcriptional responses to high-intensity light, singlet oxygen and hydrogen peroxide increased. PAR and UV-B manipulations in the field revealed that the irMAX2 bleaching phenotype is reversed by decreasing PAR, but not UV-B fluence. We propose that NaMAX2 functions in high-light adaptation and fitness optimisation by regulating high-light responses independently of its roles in the SL and KAR signalling pathways. The work provides another example of the value of studying the function of genes in the complex environments in which plants evolved, namely nature.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nicotiana / Hojas de la Planta Idioma: En Revista: Plant Cell Environ Asunto de la revista: BOTANICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nicotiana / Hojas de la Planta Idioma: En Revista: Plant Cell Environ Asunto de la revista: BOTANICA Año: 2024 Tipo del documento: Article País de afiliación: China