Evidence map›Paper›PMID 41059766›Full record

ArticleAnnals of botany2026

The BpFLA1 and BpFLA2 genes are involved in regulating secondary xylem development in Betula platyphylla and respond to artificial bending.

Yan Gao, Thi Kim Lien Phan, Jiawei Zhang, Ying Yu, Chao Wang

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Article in Annals of botany, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yan GaoState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 26 Hexing Road, 150040, China.
Thi Kim Lien PhanState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 26 Hexing Road, 150040, China.
Jiawei ZhangState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 26 Hexing Road, 150040, China.
Ying YuState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 26 Hexing Road, 150040, China.
Chao WangState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 26 Hexing Road, 150040, China.

Funding

Innovation Project of State Key Laboratory of Tree Genetics and BreedingNortheast Forestry University 2021A03
6 · The paper itself

Abstract

BACKGROUND AND

aimsFasciclin-like arabinogalactan proteins (FLAs) function in diverse plant physiological processes, particularly cell wall biosynthesis and tension wood (TW) formation. This study aimed to identify Betula platyphylla FLA genes associated with secondary xylem and TW development, thereby elucidating molecular mechanisms underlying xylogenesis to facilitate molecular improvement strategies.

methodsTissue-specific expression of two FLA genes (BpFLA1, BPFLA2) was analysed via quantitative real-time PCR. BpFLA1/2-overexpressing transgenic lines and bpfla1 knockout mutants were generated using the pROK II vector and CRISPR-Cas9 technology. Anatomical phenotypes, cell wall composition and TW development were subsequently investigated. KEY

resultsTwo FLA genes (BpFLA1, BpFLA2) were identified in the birch TW transcriptome. Phylogenetically, BpFLA1 and BpFLA2 exhibit conserved evolutionary relationships and structural domains. Both genes were highly expressed in mature stems but suppressed by mechanical stimuli. BpFLA1/2-overexpressing transgenics displayed slightly suppressed growth, reduced cell wall thickness, enlarged xylem vessel area and notably inhibited TW formation following artificial bending. Conversely, bpfla1 knockout mutants exhibited significant thickening of xylem fibre cell walls, a phenotype contrasting sharply with OE lines.

conclusionBpFLA1/2 functions as a critical regulator of cell wall development and a negative regulator of xylem fibre and TW formation in birch. Therefore, this study identifies BpFLA1/2 as a novel target for genetic improvement. BpFLA1/2 overexpression potentially enhances wood straightness and quality, whereas its suppression or knockout may benefit cellulose production for pulpwood applications.

Indexed as

BetulaGenes, PlantMucoproteinsPlant ProteinsXylemCell WallGene Expression Regulation, PlantPhylogenyPlants, Genetically ModifiedWoodarabinogalactan proteinsMucoproteinsPlant ProteinsBetula platyphyllacell wall developmentfasciclin-like arabinogalactan proteins (FLAs)secondary xylemtension wood

Identifiers

PMID41059766
PMCPMC12823244

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.