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一种用于选择普通小麦(L.)中多酚氧化酶基因无效等位基因的新共显性DNA标记的开发与验证。

Development and validation of a new co-dominant DNA marker for selecting the null allele of polyphenol oxidase gene in common wheat ( L.).

作者信息

Nakamaru Akiko, Kato Keita, Ikenaga Sachiko, Nakamura Toshiki, Hatakeyama Katsunori

机构信息

Tohoku Agricultural Research Centre, National Agricultural and Food Research Organization, 4 Akahira, Shimo-kuriyagawa, Morioka, Iwate 020-0198, Japan.

The United Graduate School of Agricultural Sciences, Iwate University, 3-18-8 Ueda, Morioka, Iwate 020-8550, Japan.

出版信息

Breed Sci. 2025 Apr;75(2):102-110. doi: 10.1270/jsbbs.24071. Epub 2025 Apr 4.

Abstract

Polyphenol oxidase (PPO) is a key enzyme contributing to the time-dependent discoloration of wheat products. Developing cultivars with low PPO activity is one way to solve this problem. In this study, we focused on the gene, which has the second highest effect on grain PPO activity after the gene. Utilizing resequencing data, we found that the gene in the common wheat line 'Fukuhonoka-NIL', which exhibits low PPO activity, has an approximately 3 kb deletion in the 3'UTR and a 73 bp deletion in the third exon. The deletion in the third exon indicated that this allele was the allele, previously identified in the wheat D genome progenitor, Coss. Additionally, the allele in 'Fukuhonoka-NIL' had very low expression, suggesting that this allele is non-functional. We developed a new co-dominant DNA marker for distinguishing the , and alleles and demonstrated that F plants homozygous for the allele exhibited significantly lower grain PPO activity. Additionally, we determined that the allele likely originated from ssp. (lineage 1) accessions. The allele has not previously been found in common wheat ( L., AABBDD genome), and thus the DNA marker developed in this study will be helpful for introducing this allele in common wheat breeding programs.

摘要

多酚氧化酶(PPO)是导致小麦制品随时间变色的关键酶。培育具有低PPO活性的品种是解决这一问题的一种方法。在本研究中,我们聚焦于该基因,其对籽粒PPO活性的影响仅次于该基因。利用重测序数据,我们发现普通小麦品系‘福光之华近等基因系’(Fukuhonoka-NIL)中表现出低PPO活性的该基因,在3'非翻译区有一个约3 kb的缺失,在第三个外显子中有一个73 bp的缺失。第三个外显子中的缺失表明该等位基因是先前在小麦D基因组祖先节节麦(Aegilops tauschii Coss.)中鉴定出的等位基因。此外,‘福光之华近等基因系’中的该等位基因表达量非常低,表明该等位基因无功能。我们开发了一种新的共显性DNA标记来区分该、该和该等位基因,并证明纯合该等位基因的F代植株籽粒PPO活性显著降低。此外,我们确定该等位基因可能起源于节节麦(Aegilops tauschii ssp. strangulata (lineage 1))种质。该等位基因此前未在普通小麦(Triticum aestivum L., AABBDD基因组)中发现,因此本研究开发的DNA标记将有助于在普通小麦育种计划中引入该等位基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/417d/12395200/b4c1135e4451/75_102-g001.jpg

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