The role of the Golden2-like (GLK) transcription factor in regulating terpenoid indole alkaloid biosynthesis in Catharanthus roseus

被引:3
|
作者
Cole-Osborn, Lauren F. [1 ,2 ]
Mccallan, Shannon A. [3 ]
Prifti, Olga [2 ]
Abu, Rafay [3 ]
Sjoelund, Virginie [3 ]
Lee-Parsons, Carolyn W. T. [1 ,2 ,3 ]
机构
[1] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
[2] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
[3] Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USA
关键词
GLK; Golden2-like transcription factor; Catharanthus roseus; Terpenoid indole alkaloid; Chloroplast retrograde signaling; Lincomycin; GENE-EXPRESSION; CHLOROPLAST DEVELOPMENT; VINDOLINE BIOSYNTHESIS; FACTORS COORDINATE; METHYL JASMONATE; LEAF SENESCENCE; PLANT DEFENSE; ARABIDOPSIS; LIGHT; PATHWAY;
D O I
10.1007/s00299-024-03208-9
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Catharanthus roseus is the sole source of the chemotherapeutic terpenoid indole alkaloids (TIAs) vinblastine and vincristine. TIA pathway genes, particularly genes in the vindoline pathway, are expressed at higher levels in immature versus mature leaves, but the molecular mechanisms responsible for this developmental regulation are unknown. We investigated the role of GOLDEN2-LIKE (GLK) transcription factors in contributing to this ontogenetic regulation since GLKs are active in seedlings upon light exposure and in the leaf's early development, but their activity is repressed as leaves age and senesce. We identified a GLK homologue in C. roseus and functionally characterized its role in regulating TIA biosynthesis, with a focus on the vindoline pathway, by transiently reducing its expression through two separate methods: virus-induced gene silencing (VIGS) and application of chloroplast retrograde signaling inducers, norflurazon and lincomycin. Reducing CrGLK levels with each method reduced chlorophyll accumulation and the expression of the light harvesting complex subunit (LHCB2.2), confirming its functional homology with GLKs in other plant species. In contrast, reducing CrGLK via VIGS or lincomycin increased TIA accumulation and TIA pathway gene expression, suggesting that CrGLK may repress TIA biosynthesis. However, norflurazon had no effect on TIA gene expression, indicating that reducing CrGLK alone is not sufficient to induce TIA biosynthesis. Future work is needed to clarify the specific molecular mechanisms leading to increased TIA biosynthesis with CrGLK silencing. This is the first identification and characterization of GLK in C. roseus and the first investigation of how chloroplast retrograde signaling might regulate TIA biosynthesis.
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页数:20
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