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鉴定和基于图谱的 EMS 诱导的小麦 TaSP1 基因与穗结构相关的突变体克隆。

Identification and map-based cloning of an EMS-induced mutation in wheat gene TaSP1 related to spike architecture.

机构信息

School of Life Sciences, Henan University, Kaifeng, 475001, China.

State Key Laboratory of Crop Stress Adaptation and Improvement, College of Agriculture, Henan University, Kaifeng, 475001, Henan, China.

出版信息

Theor Appl Genet. 2024 May 6;137(6):119. doi: 10.1007/s00122-024-04621-0.

Abstract

A candidate gene TaSP1 related to spike shape was cloned, and the gene-specific marker was developed to efficiently track the superior haplotype in common wheat. Spike shape, an important factor that affects wheat grain yield, is mainly defined by spike length (SPL), spikelet number (SPN), and compactness. Zhoumai32 mutant 1160 (ZM1160), a mutant obtained from ethyl methane sulfonate (EMS) treatment of hexaploid wheat variety Zhoumai32, was used to identify and clone the candidate gene that conditioned the spike shape. Genetic analysis of an F population derived from a cross of ZM1160 and Bainong207 suggested that the compact spike shape in ZM1160 was controlled by a single recessive gene, and therefore, the mutated gene was designated as Tasp1. With polymorphic markers identified through bulked segregant analysis (BSA), the gene was mapped to a 2.65-cM interval flanked by markers YZU0852 and MIS46239 on chromosome 7D, corresponding to a 0.42-Mb physical interval of Chinese spring (CS) reference sequences (RefSeq v1.0). To fine map TaSP1, 15 and seven recombinants were, respectively, screened from 1599 and 1903 F plants derived from the heterozygous F plants. Finally, TaSP1 was delimited to a 21.9 Kb (4,870,562 to 4,892,493 bp) Xmis48123-Xmis48104 interval. Only one high-confidence gene TraesCS7D02G010200 was annotated in this region, which encodes an unknown protein with a putative vWA domain. Quantitative reverse transcription PCR (qRT-PCR) analysis showed that TraesCS7D02G010200 was mainly expressed in the spike. Haplotype analysis of 655 wheat cultivars using the candidate gene-specific marker Xg010200p2 identified a superior haplotype TaSP1b with longer spike and more spikelet number. TaSP1 is beneficial to the improvement in wheat spike shape.

摘要

克隆了一个与穗型相关的候选基因 TaSP1,并开发了基因特异性标记来有效地跟踪普通小麦中的优良单倍型。穗型是影响小麦粒重的重要因素,主要由穗长(SPL)、小穗数(SPN)和紧凑度决定。ZM1160 是从六倍体小麦品种周麦 32 用甲基磺酸乙酯(EMS)处理获得的突变体 1160,用于鉴定和克隆调节穗型的候选基因。ZM1160 与白农 207 杂交衍生的 F 群体的遗传分析表明,ZM1160 紧凑的穗型受单个隐性基因控制,因此,突变基因被命名为 Tasp1。通过 bulked segregant analysis(BSA)鉴定的多态性标记将该基因定位在 7D 染色体上标记 YZU0852 和 MIS46239 之间的 2.65-cM 区间内,对应于中国春(CS)参考序列(RefSeq v1.0)的 0.42-Mb 物理区间。为了精细定位 TaSP1,分别从杂合 F 植物衍生的 1599 和 1903 F 植物中筛选出 15 和 7 个重组体。最后,TaSP1 被限定在一个 21.9 Kb(4,870,562 到 4,892,493 bp)的 Xmis48123-Xmis48104 区间内。该区域仅注释了一个高度置信的基因 TraesCS7D02G010200,该基因编码具有推定 vWA 结构域的未知蛋白。使用候选基因特异性标记 Xg010200p2 对 655 个小麦品种进行的定量逆转录 PCR(qRT-PCR)分析表明,TraesCS7D02G010200 主要在穗中表达。利用候选基因特异性标记 Xg010200p2 对 655 个小麦品种进行的单倍型分析鉴定出具有较长穗和更多小穗数的优良单倍型 TaSP1b。TaSP1 有利于改善小麦穗型。

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