• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

玉米自发单倍体加倍的主效 QTL qshgd1 的精细定位。

Fine mapping of major QTL qshgd1 for spontaneous haploid genome doubling in maize (Zea mays L.).

机构信息

Department of Agronomy, Iowa State University, Ames, IA, 50011, USA.

KWS SAAT SE & Co. KGaA, Grimsehlstr. 31, 37574, Einbeck, Germany.

出版信息

Theor Appl Genet. 2024 May 3;137(5):117. doi: 10.1007/s00122-024-04615-y.

DOI:10.1007/s00122-024-04615-y
PMID:38700534
Abstract

A large-effect QTL was fine mapped, which revealed 79 gene models, with 10 promising candidate genes, along with a novel inversion. In commercial maize breeding, doubled haploid (DH) technology is arguably the most efficient resource for rapidly developing novel, completely homozygous lines. However, the DH strategy, using in vivo haploid induction, currently requires the use of mutagenic agents which can be not only hazardous, but laborious. This study focuses on an alternative approach to develop DH lines-spontaneous haploid genome duplication (SHGD) via naturally restored haploid male fertility (HMF). Inbred lines A427 and Wf9, the former with high HMF and the latter with low HMF, were selected to fine-map a large-effect QTL associated with SHGD-qshgd1. SHGD alleles were derived from A427, with novel haploid recombinant groups having varying levels of the A427 chromosomal region recovered. The chromosomal region of interest is composed of 45 megabases (Mb) of genetic information on chromosome 5. Significant differences between haploid recombinant groups for HMF were identified, signaling the possibility of mapping the QTL more closely. Due to suppression of recombination from the proximity of the centromere, and a newly discovered inversion region, the associated QTL was only confined to a 25 Mb region, within which only a single recombinant was observed among ca. 9,000 BC individuals. Nevertheless, 79 gene models were identified within this 25 Mb region. Additionally, 10 promising candidate genes, based on RNA-seq data, are described for future evaluation, while the narrowed down genome region is accessible for straightforward introgression into elite germplasm by BC methods.

摘要

一个大效应 QTL 被精细定位,揭示了 79 个基因模型,其中有 10 个有希望的候选基因,以及一个新的倒位。在商业玉米育种中,双单倍体(DH)技术可以说是快速开发新型、完全纯合系的最有效资源。然而,DH 策略,使用体内单倍体诱导,目前需要使用诱变剂,这不仅危险,而且费力。本研究专注于一种替代方法来开发 DH 系-自发单倍体基因组复制(SHGD)通过自然恢复的单倍体雄性育性(HMF)。选择自交系 A427 和 Wf9 进行精细定位与 SHGD-qshgd1 相关的大效应 QTL,前者具有高 HMF,后者具有低 HMF。SHGD 等位基因来自 A427,具有不同水平的 A427 染色体区域恢复的新型单倍体重组群体。感兴趣的染色体区域由 5 号染色体上 4500 万个碱基对(Mb)的遗传信息组成。在 HMF 方面,单倍体重组群体之间存在显著差异,这表明有可能更紧密地定位 QTL。由于近着丝粒重组的抑制,以及一个新发现的倒位区域,相关的 QTL 仅局限于 25 Mb 区域,在大约 9000 个 BC 个体中,只观察到一个重组体。然而,在这个 25 Mb 区域内鉴定出了 79 个基因模型。此外,根据 RNA-seq 数据,描述了 10 个有前途的候选基因,以供未来评估,而缩小的基因组区域可通过 BC 方法直接导入到优良种质中。

相似文献

1
Fine mapping of major QTL qshgd1 for spontaneous haploid genome doubling in maize (Zea mays L.).玉米自发单倍体加倍的主效 QTL qshgd1 的精细定位。
Theor Appl Genet. 2024 May 3;137(5):117. doi: 10.1007/s00122-024-04615-y.
2
Mapping of QTL and identification of candidate genes conferring spontaneous haploid genome doubling in maize (Zea mays L.).定位控制玉米自发单倍体加倍的 QTL 并鉴定候选基因。
Plant Sci. 2020 Apr;293:110337. doi: 10.1016/j.plantsci.2019.110337. Epub 2019 Nov 21.
3
Major locus for spontaneous haploid genome doubling detected by a case-control GWAS in exotic maize germplasm.通过对异源玉米种质的病例对照 GWAS 检测到自发单倍体基因组加倍的主要基因座。
Theor Appl Genet. 2021 May;134(5):1423-1434. doi: 10.1007/s00122-021-03780-8. Epub 2021 Feb 5.
4
QTL mapping of spontaneous haploid genome doubling using genotyping-by-sequencing in maize (Zea mays L.).利用测序基因分型对玉米(Zea mays L.)自发单倍体基因组加倍进行QTL定位。
Theor Appl Genet. 2020 Jul;133(7):2131-2140. doi: 10.1007/s00122-020-03585-1. Epub 2020 Apr 13.
5
QTL mapping for haploid male fertility by a segregation distortion method and fine mapping of a key QTL qhmf4 in maize.利用偏分离方法对玉米单倍体雄育性进行QTL定位及关键QTL qhmf4的精细定位
Theor Appl Genet. 2017 Jul;130(7):1349-1359. doi: 10.1007/s00122-017-2892-6. Epub 2017 Apr 7.
6
Usefulness of temperate-adapted maize lines developed by doubled haploid and single-seed descent methods.双单倍体和单籽传代法选育的温带玉米自交系的有用性。
Theor Appl Genet. 2022 Jun;135(6):1829-1841. doi: 10.1007/s00122-022-04075-2. Epub 2022 Mar 19.
7
Maize In Planta Haploid Inducer Lines: A Cornerstone for Doubled Haploid Technology.玉米植株内单倍体诱导系:双单倍体技术的基石
Methods Mol Biol. 2021;2288:25-48. doi: 10.1007/978-1-0716-1335-1_2.
8
Protocols for In Vivo Doubled Haploid (DH) Technology in Maize Breeding: From Haploid Inducer Development to Haploid Genome Doubling.玉米育种中体内双单倍体(DH)技术的规程:从单倍体诱导系的培育到单倍体基因组加倍
Methods Mol Biol. 2022;2484:213-235. doi: 10.1007/978-1-0716-2253-7_16.
9
Haploid male fertility and spontaneous chromosome doubling evaluated in a diallel and recurrent selection experiment in maize.在玉米的完全双列杂交和轮回选择试验中评估单倍体雄配子体育性和自发染色体加倍。
Theor Appl Genet. 2019 Aug;132(8):2273-2284. doi: 10.1007/s00122-019-03353-w. Epub 2019 May 6.
10
Fine mapping of qhir8 affecting in vivo haploid induction in maize.影响玉米体内单倍体诱导的qhir8精细定位
Theor Appl Genet. 2015 Dec;128(12):2507-15. doi: 10.1007/s00122-015-2605-y. Epub 2015 Oct 6.

引用本文的文献

1
Genes and genetics belong to maize haploid induction.基因与遗传学在玉米单倍体诱导中发挥作用。
Front Plant Sci. 2025 Aug 5;16:1634053. doi: 10.3389/fpls.2025.1634053. eCollection 2025.
2
Genetic variation and heritability of haploid frailty in maize.玉米单倍体脆弱性的遗传变异与遗传力
Front Plant Sci. 2025 Jun 3;16:1572901. doi: 10.3389/fpls.2025.1572901. eCollection 2025.
3
Association mapping of haploid male fertility in sweet corn.甜玉米单倍体雄性育性的关联分析

本文引用的文献

1
Haploid male fertility is restored by parallel spindle genes in Arabidopsis thaliana.拟南芥中平行纺锤体基因可恢复单倍体雄性育性。
Nat Plants. 2023 Feb;9(2):214-218. doi: 10.1038/s41477-022-01332-6. Epub 2023 Jan 9.
2
Usefulness of temperate-adapted maize lines developed by doubled haploid and single-seed descent methods.双单倍体和单籽传代法选育的温带玉米自交系的有用性。
Theor Appl Genet. 2022 Jun;135(6):1829-1841. doi: 10.1007/s00122-022-04075-2. Epub 2022 Mar 19.
3
CircNFIC Balances Inflammation and Apoptosis by Sponging miR-30e-3p and Regulating DENND1B Expression.
Theor Appl Genet. 2025 Apr 16;138(5):102. doi: 10.1007/s00122-025-04888-x.
环状非编码 RNA NFIC 通过海绵吸附 miR-30e-3p 并调控 DENND1B 表达来平衡炎症和细胞凋亡。
Genes (Basel). 2021 Nov 19;12(11):1829. doi: 10.3390/genes12111829.
4
De novo assembly, annotation, and comparative analysis of 26 diverse maize genomes.从头组装、注释和 26 个不同玉米基因组的比较分析。
Science. 2021 Aug 6;373(6555):655-662. doi: 10.1126/science.abg5289.
5
Major locus for spontaneous haploid genome doubling detected by a case-control GWAS in exotic maize germplasm.通过对异源玉米种质的病例对照 GWAS 检测到自发单倍体基因组加倍的主要基因座。
Theor Appl Genet. 2021 May;134(5):1423-1434. doi: 10.1007/s00122-021-03780-8. Epub 2021 Feb 5.
6
LoxTnSeq: random transposon insertions combined with cre/lox recombination and counterselection to generate large random genome reductions.LoxTnSeq:随机转座子插入与 Cre/lox 重组和反选择相结合,以产生大规模随机基因组减少。
Microb Biotechnol. 2021 Nov;14(6):2403-2419. doi: 10.1111/1751-7915.13714. Epub 2020 Dec 16.
7
Puzzling out plant reproduction by haploid induction for innovations in plant breeding.通过单倍体诱导破解植物繁殖之谜,推动植物育种创新。
Nat Plants. 2020 Jun;6(6):610-619. doi: 10.1038/s41477-020-0664-9. Epub 2020 Jun 8.
8
QTL mapping of spontaneous haploid genome doubling using genotyping-by-sequencing in maize (Zea mays L.).利用测序基因分型对玉米(Zea mays L.)自发单倍体基因组加倍进行QTL定位。
Theor Appl Genet. 2020 Jul;133(7):2131-2140. doi: 10.1007/s00122-020-03585-1. Epub 2020 Apr 13.
9
Impact of Spontaneous Haploid Genome Doubling in Maize Breeding.自发单倍体基因组加倍在玉米育种中的影响
Plants (Basel). 2020 Mar 17;9(3):369. doi: 10.3390/plants9030369.
10
Mapping of QTL and identification of candidate genes conferring spontaneous haploid genome doubling in maize (Zea mays L.).定位控制玉米自发单倍体加倍的 QTL 并鉴定候选基因。
Plant Sci. 2020 Apr;293:110337. doi: 10.1016/j.plantsci.2019.110337. Epub 2019 Nov 21.