4.7 Article

The NAC transcription factor ClNAC68 positively regulates sugar content and seed development in watermelon by repressing ClINV and ClGH3.6

Journal

HORTICULTURE RESEARCH
Volume 8, Issue 1, Pages -

Publisher

NANJING AGRICULTURAL UNIV
DOI: 10.1038/s41438-021-00649-1

Keywords

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Funding

  1. Collaborative Innovation Center of BAAFS [KJCX201907-2]
  2. Beijing Science & Technology Program [D171100007617001]
  3. National Key R&D Program of China [2018YFD0100703]
  4. National Natural Science Foundation of China [31930096, 1902034]
  5. Beijing Natural Science Foundation [6204038, 6202010]
  6. Beijing Scholar Program [BSP026, YBSP019]

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NAC transcription factor ClNAC68 plays a crucial role in fruit ripening and quality by repressing the expression of sucrose metabolism related genes and the IAA signaling pathway gene. Knockout of ClNAC68 leads to decreased soluble solid content and sucrose accumulation in fruit flesh, delayed development and inhibited germination in seeds, and reduced IAA content. These findings provide new insights into how NAC transcription factors affect fruit quality and seed development.
NAC (NAM, ATAF1/2, and CUC2) transcription factors play important roles in fruit ripening and quality. The watermelon genome encodes 80 NAC genes, and 21 of these NAC genes are highly expressed in both the flesh and vascular tissues. Among these genes, ClNAC68 expression was significantly higher in flesh than in rind. However, the intrinsic regulatory mechanism of ClNAC68 in fruit ripening and quality is still unknown. In this study, we found that ClNAC68 is a transcriptional repressor and that the repression domain is located in the C-terminus. Knockout of ClNAC68 by the CRISPR-Cas9 system decreased the soluble solid content and sucrose accumulation in mutant flesh. Development was delayed, germination was inhibited, and the IAA content was significantly decreased in mutant seeds. Transcriptome analysis showed that the invertase gene ClINV was the only gene involved in sucrose metabolism that was upregulated in mutant flesh, and expression of the indole-3-acetic acid-amido synthetase gene ClGH3.6 in the IAA signaling pathway was also induced in mutant seeds. EMSA and dual-luciferase assays showed that ClNAC68 directly bound to the promoters of ClINV and ClGH3.6 to repress their expression. These results indicated that ClNAC68 positively regulated sugar and IAA accumulation by repressing ClINV and ClGH3.6. Our findings provide new insights into the regulatory mechanisms by which NAC transcription factors affect fruit quality and seed development.

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