A High Soluble-Fibre Allele in Wheat Encodes a Defective Cell Wall Peroxidase Responsible for Dimerization of Ferulate Moieties on Arabinoxylan.

IF 10.5 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Plant Biotechnology Journal Pub Date : 2026-05-01 Epub Date: 2026-01-03 DOI:10.1111/pbi.70527
Rowan A C Mitchell, Ondrej Kosik, Abdul Kader Alabdullah, Anneke Prins, Maria Oszvald, Till K Pellny, Jackie Freeman, Kirstie Halsey, Caroline A Sparks, Alison Huttly, James Brett, Michelle Leverington-Waite, Simon Griffiths, Peter R Shewry, Alison Lovegrove
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Abstract

Increasing dietary fibre (DF) intake is an important target to improve health. An attractive strategy for this is to increase DF in wheat which is derived principally from the endosperm cell wall polysaccharide arabinoxylan (AX). The water-extractable form of this (WE-AX) accounts for most soluble dietary fibre (SDF), which is believed to confer particular health benefits. A region of chromosome 6B in some wheat varieties confers high SDF and here we show that the cause is an allele encoding a peroxidase family protein with a single residue change (PER1-v) associated with high WE-AX, compared to the more common form (PER1). Both wheat lines carrying this natural PER1-v variant and those with an induced knockout mutation of PER1 showed reduced dimerization of endosperm ferulate consistent with a mechanism of decreased cross-linking in the cell wall that increases WE-AX. Transiently expressed PER1_RFP fusion protein driven by the native promoter in wheat endosperm was shown to localise to cell walls, whereas PER1-v_RFP did not. We therefore propose that PER1-v lacks the capacity to dimerise AX ferulate in vivo due to mis-localisation caused by the missense single-nucleotide polymorphism (SNP) in the PER1-v allele, so that the SNP acts as a perfect marker. This marker can be used to identify current wheat varieties with high WE-AX to be used by processors and by breeders to ensure future varieties have high WE-AX to make healthier wheat-based foods.

小麦高可溶性纤维等位基因编码有缺陷的细胞壁过氧化物酶,负责阿拉伯木聚糖上阿魏酸部分的二聚化。
增加膳食纤维(DF)的摄入量是改善健康的重要目标。一个有吸引力的策略是增加小麦的DF, DF主要来自胚乳细胞壁多糖阿拉伯木聚糖(AX)。这种水萃取形式(WE-AX)占大多数可溶性膳食纤维(SDF),被认为对健康特别有益。在一些小麦品种中,染色体6B的一个区域赋予了高SDF,在这里,我们表明,与更常见的形式(PER1)相比,编码过氧化物酶家族蛋白的一个等位基因具有单一残基变化(PER1-v),与高we - ax相关。携带这种天然PER1-v变异的小麦品系和诱导PER1基因敲除突变的小麦品系都显示,胚乳阿魏酸二聚化减少,这与细胞壁交联减少增加WE-AX的机制一致。由天然启动子驱动的瞬时表达的PER1_RFP融合蛋白在小麦胚乳中被证明定位到细胞壁,而PER1-v_RFP则没有定位到细胞壁。因此,我们认为PER1-v在体内缺乏对阿魏酸AX二聚的能力,这是由于PER1-v等位基因中的错意单核苷酸多态性(SNP)导致的错误定位,因此SNP可以作为一个完美的标记。该标记可用于识别目前具有高WE-AX的小麦品种,供加工商和育种者使用,以确保未来的品种具有高WE-AX,以生产更健康的小麦食品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plant Biotechnology Journal
Plant Biotechnology Journal 生物-生物工程与应用微生物
CiteScore
20.50
自引率
2.90%
发文量
201
审稿时长
1 months
期刊介绍: Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.
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