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Correlation Analysis of Lignin Accumulation and Expression of Key Genes Involved in Lignin Biosynthesis of Ramie ()

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2019 May 25
PMID 31121827
Citations 16
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Abstract

The phloem of the stem of ramie () is an important source of natural fiber for the textile industry. However, the lignin content in the phloem affects the quality of ramie phloem fiber. In this study, the lignin content and related key gene expression levels were analyzed in the phloem and xylem at different developmental periods. The results showed that the relative expression levels of lignin synthesis-related key genes in the xylem and phloem of the stem gradually decreased from the fast-growing period to the late maturation period, but the corresponding lignin content increased significantly. However, the relative expression levels of a few genes were the highest during the maturation period. During all three periods, the lignin content in ramie stems was positively correlated with the expression of genes, including , and in the phenylpropanoid pathway, and in the lignin-specific synthetic pathway, and in the downstream pathway of lignin synthesis, but the lignin content was negatively correlated with the expression of genes including in the phenylpropanoid pathway and in the shunt pathway of lignin monomer synthesis. The ramie 4CL3 recombinant protein prefers cinnamic acid as a substrate during catalysis, and it negatively regulates lignin synthesis. It is speculated that ramie is mainly involved in the synthesis of ramie flavonoid compounds, and that is mainly involved in lignin synthesis.

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References
1.
Kandimalla R, Kalita S, Choudhury B, Devi D, Kalita D, Kalita K . Fiber from ramie plant (Boehmeria nivea): A novel suture biomaterial. Mater Sci Eng C Mater Biol Appl. 2016; 62:816-22. DOI: 10.1016/j.msec.2016.02.040. View

2.
Silber M, Meimberg H, Ebel J . Identification of a 4-coumarate:CoA ligase gene family in the moss, Physcomitrella patens. Phytochemistry. 2008; 69(13):2449-56. DOI: 10.1016/j.phytochem.2008.06.014. View

3.
Whetten R, Sederoff R . Lignin Biosynthesis. Plant Cell. 1995; 7(7):1001-1013. PMC: 160901. DOI: 10.1105/tpc.7.7.1001. View

4.
de Vries J, de Vries S, Slamovits C, Rose L, Archibald J . How Embryophytic is the Biosynthesis of Phenylpropanoids and their Derivatives in Streptophyte Algae?. Plant Cell Physiol. 2017; 58(5):934-945. DOI: 10.1093/pcp/pcx037. View

5.
Sorensen I, Pettolino F, Bacic A, Ralph J, Lu F, ONeill M . The charophycean green algae provide insights into the early origins of plant cell walls. Plant J. 2011; 68(2):201-11. DOI: 10.1111/j.1365-313X.2011.04686.x. View