在一个小麦 EMS 突变体中,一个剪接位点的单碱基变化导致了 Wx-A1 基因的错误 RNA 剪接和基因失活。

A single-base change at a splice site in Wx-A1 caused incorrect RNA splicing and gene inactivation in a wheat EMS mutant line.

机构信息

Triticeae Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.

CSIRO Agriculture and Food, Black Mountain, Canberra, ACT, 2601, Australia.

出版信息

Theor Appl Genet. 2019 Jul;132(7):2097-2109. doi: 10.1007/s00122-019-03340-1. Epub 2019 Apr 16.

Abstract

An EMS-induced single-base mutation at a splice site caused abnormal RNA splicing and resulted in the gene inactivation and the lack of Wx-A1 protein in a wheat EMS mutant line. An EMS-mutagenized population was generated using common wheat cv. SM126 consisting of 10,600 M2 plants. One Wx-A1 null mutant was identified through analyses of 390 grains produced from 130 M2 plants using electrophoresis analyses. The Wx-A1 sequences of parental line SM126 and M2-31 mutant were determined as 2781 bp, and there was only one SNP mutation between them. The SNP was a mutation from G to A at nucleotide sequence position 2168 bp (G2168A) downstream of the start codon which was located at the splicing site within the eighth intron. All 52 cDNA transcripts were found to be incorrectly spliced and can be summarized as five types of variations. The deletion of the exon and the exclusion of intron were structural features in abnormal splicing RNA. Together with the prediction of potential splice regulatory motifs, the mutation G2168A happened within the 5' splice site of the eighth intron and destroyed the splice donor site from GU to AU, which may have brought about a barrier against correct RNA splice, and generated abnormal mRNA, which was the mechanism of the inactivation of Wx-A1 in M2-31. The lack of Wx-A1 has resulted in changes in starch properties in the M2-31 mutant, with the reduction in amylose and starch contents. The increased grains hardness was observed in M2-31, which may be related to the lower expression level of Pinb-D1 gene. As the waxy wheat foods have a lot of advantages, the null waxy genes will be widely applied in breeding waxy wheat for varied amylose contents.

摘要

一个 EMS 诱导的剪接位点上的单碱基突变导致异常的 RNA 剪接,从而使基因失活,导致小麦 EMS 突变体系中缺乏 Wx-A1 蛋白。使用包含 10600 株 M2 植物的普通小麦品种 SM126 生成了一个 EMS 诱变群体。通过对 130 株 M2 植物产生的 390 粒种子进行电泳分析,鉴定出一个 Wx-A1 缺失突变体。亲本系 SM126 和 M2-31 突变体的 Wx-A1 序列分别为 2781bp,它们之间只有一个 SNP 突变。SNP 是在起始密码子下游的核苷酸序列位置 2168bp 处由 G 突变为 A(G2168A),该位置位于第八内含子的剪接位点内。所有 52 个 cDNA 转录物均发现异常剪接,可归纳为五种类型的变异。外显子缺失和内含子缺失是异常剪接 RNA 的结构特征。结合潜在剪接调控基序的预测,突变 G2168A 发生在第八内含子的 5'剪接位点内,破坏了从 GU 到 AU 的剪接供体位点,这可能导致正确的 RNA 剪接受阻,并产生异常的 mRNA,这是 M2-31 中 Wx-A1 失活的机制。Wx-A1 的缺失导致 M2-31 突变体中淀粉性质发生变化,直链淀粉和淀粉含量降低。在 M2-31 中观察到籽粒硬度增加,这可能与 Pinb-D1 基因表达水平较低有关。由于蜡质小麦食品具有许多优势,无蜡质基因将广泛应用于不同直链淀粉含量的蜡质小麦的育种中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索