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Updated: Feb 10, 2026

Label-free in situ Imaging of Lignification in Plant Cell Walls
Published on: November 1, 2010
PbrmiR397a regulates lignification during stone cell development in pear fruit
Cheng Xue1, Jia-Long Yao2, Meng-Fan Qin1
1Center of Pear Engineering Technology Research, State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing, Jiangsu, China.
MicroRNA miR397a inhibits laccase genes, reducing lignin and stone cells in pear fruit. A specific genetic variation in miR397a is linked to lower lignin, offering insights for improving fruit quality.
Area of Science:
- Plant Molecular Biology
- Agricultural Science
- Biochemistry
Background:
- Lignified stone cells negatively impact fruit quality, necessitating genetic strategies to control their development.
- The precise molecular mechanisms governing lignification in fruit stone cells remain largely unelucidated.
- Understanding these mechanisms is crucial for developing methods to enhance fruit characteristics.
Purpose of the Study:
- To investigate the role of microRNA (miR) miR397a in regulating lignin biosynthesis and stone cell formation in fruit.
- To identify molecular targets and genetic factors influencing miR397a activity in relation to fruit quality.
Main Methods:
- Transient overexpression of Chinese pear miR397a (PbrmiR397a) and silencing of laccase (LAC) genes in pear fruit.
- Analysis of a single nucleotide polymorphism (SNP) in the PbrmiR397a promoter across 60 pear varieties.
- Cell-based assays to confirm the function of the SNP and its response to salicylic acid.
- Stable overexpression of PbrmiR397a in transgenic tobacco plants to assess effects on lignin and cell wall structure.
Main Results:
- Overexpression of PbrmiR397a and LAC gene silencing significantly reduced lignin content and stone cell numbers in pear fruit.
- A promoter SNP in PbrmiR397a was associated with reduced fruit lignin and created a salicylic acid-responsive element.
- Transgenic tobacco plants overexpressing PbrmiR397a exhibited decreased LAC gene expression, lower lignin content, and altered vessel element structure.
Conclusions:
- miR397a acts as a negative regulator of lignin biosynthesis by targeting LAC genes in fruit.
- A naturally occurring SNP in the PbrmiR397a promoter influences lignin levels and offers a potential marker for breeding.
- This research provides valuable molecular insights for genetic improvement of fruit quality by controlling stone cell development.
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