• 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

基于驯化基因对‘agriocrithon’起源的阐明质疑了西藏是大麦驯化中心之一的假说。

Elucidation of the origin of 'agriocrithon' based on domestication genes questions the hypothesis that Tibet is one of the centers of barley domestication.

机构信息

National Institute of Agrobiological Sciences, Tsukuba, 305-8602, Japan.

Faculty of Science, Plant Breeding Institute, The University of Sydney, Cobbitty, NSW, 2570, Australia.

出版信息

Plant J. 2018 May;94(3):525-534. doi: 10.1111/tpj.13876. Epub 2018 Apr 6.

DOI:10.1111/tpj.13876
PMID:29469199
Abstract

Wild barley forms a two-rowed spike with a brittle rachis whereas domesticated barley has two- or six-rowed spikes with a tough rachis. Like domesticated barley, 'agriocrithon' forms a six-rowed spike; however, the spike is brittle as in wild barley, which makes the origin of agriocrithon obscure. Haplotype analysis of the Six-rowed spike 1 (vrs1) and Non-brittle rachis 1 (btr1) and 2 (btr2) genes was conducted to infer the origin of agriocrithon barley. Some agriocrithon barley accessions (eu-agriocrithon) carried Btr1 and Btr2 haplotypes that are not found in any cultivars, implying that they are directly derived from wild barley through a mutation at the vrs1 locus. Other agriocrithon barley accessions (pseudo-agriocrithon) carried Btr1 or Btr2 from cultivated barley, thus implying that they originated from hybridization between six-rowed landraces carrying btr1Btr2 and Btr1btr2 genotypes followed by recombination to produce Btr1Btr2. All materials we collected from Tibet belong to pseudo-agriocrithon and thus do not support the Tibetan Plateau as being a center of barley domestication. Tracing the evolutionary history of these allelic variants revealed that eu-agriocrithon represents six-rowed barley lineages that were selected by early farmers, once in south-eastern Turkmenistan (vrs1.a1) and again in the eastern part of Uzbekistan (vrs1.a4).

摘要

野生大麦形成二棱小穗,穗轴易碎,而栽培大麦形成二棱或六棱小穗,穗轴坚韧。与栽培大麦一样,“agriocrithon”形成六棱小穗;然而,小穗像野生大麦一样易碎,这使得 agriocrithon 的起源模糊不清。对六棱小穗 1(vrs1)和非易碎穗轴 1(btr1)和 2(btr2)基因的单倍型分析推断了 agriocrithon 大麦的起源。一些 agriocrithon 大麦品种(eu-agriocrithon)携带的 Btr1 和 Btr2 单倍型在任何品种中都没有发现,这表明它们是通过 vrs1 基因座的突变直接从野生大麦中衍生而来的。其他 agriocrithon 大麦品种(pseudo-agriocrithon)携带来自栽培大麦的 Btr1 或 Btr2,这表明它们起源于携带 btr1Btr2 和 Btr1btr2 基因型的六棱地方品种之间的杂交,然后通过重组产生 Btr1Btr2。我们从西藏收集的所有材料都属于 pseudo-agriocrithon,因此不支持青藏高原是大麦驯化的中心。这些等位变异的进化历史表明,eu-agriocrithon 代表了被早期农民选择的六棱大麦谱系,一次是在土库曼斯坦东南部(vrs1.a1),另一次是在乌兹别克斯坦东部(vrs1.a4)。

相似文献

1
Elucidation of the origin of 'agriocrithon' based on domestication genes questions the hypothesis that Tibet is one of the centers of barley domestication.基于驯化基因对‘agriocrithon’起源的阐明质疑了西藏是大麦驯化中心之一的假说。
Plant J. 2018 May;94(3):525-534. doi: 10.1111/tpj.13876. Epub 2018 Apr 6.
2
Most Tibetan weedy barleys originated via recombination between Btr1 and Btr2 in domesticated barley.大多数西藏杂草大麦起源于驯化大麦中 Btr1 和 Btr2 之间的重组。
Plant Commun. 2024 May 13;5(5):100828. doi: 10.1016/j.xplc.2024.100828. Epub 2024 Jan 30.
3
On the origin of six-rowed barley with brittle rachis, agriocrithon [Hordeum vulgare ssp. vulgare f. agriocrithon (Aberg) Bowd.], based on a DNA marker closely linked to the vrs1 (six-row gene) locus.基于与vrs1(六行基因)位点紧密连锁的DNA标记,探讨具脆穗轴六行大麦agriocrithon [大麦(Hordeum vulgare)普通亚种agriocrithon(阿贝格)鲍德变种]的起源。
Theor Appl Genet. 2004 Dec;110(1):145-50. doi: 10.1007/s00122-004-1816-4. Epub 2004 Oct 30.
4
A phylogenetic analysis based on nucleotide sequence of a marker linked to the brittle rachis locus indicates a diphyletic origin of barley.基于与脆穗轴基因座连锁的一个标记的核苷酸序列进行的系统发育分析表明大麦具有双系起源。
Ann Bot. 2007 Nov;100(5):1009-15. doi: 10.1093/aob/mcm129. Epub 2007 Jul 15.
5
Population genetics and phylogenetic analysis of the vrs1 nucleotide sequence in wild and cultivated barley.野生和栽培大麦中vrs1核苷酸序列的群体遗传学与系统发育分析
Genome. 2014 Apr;57(4):239-44. doi: 10.1139/gen-2014-0039. Epub 2014 Jun 27.
6
High-density AFLP map of nonbrittle rachis 1 (btr1) and 2 (btr2) genes in barley (Hordeum vulgare L.).大麦(Hordeum vulgare L.)中脆穗轴1(btr1)和脆穗轴2(btr2)基因的高密度AFLP图谱。
Theor Appl Genet. 2004 Sep;109(5):986-95. doi: 10.1007/s00122-004-1710-0. Epub 2004 Jul 31.
7
Six-rowed barley originated from a mutation in a homeodomain-leucine zipper I-class homeobox gene.六行大麦起源于一个同源异型结构域-亮氨酸拉链I类同源框基因的突变。
Proc Natl Acad Sci U S A. 2007 Jan 23;104(4):1424-9. doi: 10.1073/pnas.0608580104. Epub 2007 Jan 12.
8
Genetic and molecular characterization of determinant of six-rowed spike of barley carrying vrs1.a4.携带 vrs1.a4 的六棱大麦穗决定因子的遗传和分子特征。
Theor Appl Genet. 2021 Oct;134(10):3225-3236. doi: 10.1007/s00122-021-03887-y. Epub 2021 Jun 16.
9
Six-rowed wild-growing barleys are hybrids of diverse origins.六棱野生大麦是多种起源的杂种。
Plant J. 2022 Aug;111(3):849-858. doi: 10.1111/tpj.15861. Epub 2022 Jun 23.
10
Haplotype structure at seven barley genes: relevance to gene pool bottlenecks, phylogeny of ear type and site of barley domestication.七个大麦基因的单倍型结构:与基因库瓶颈、穗型系统发育及大麦驯化地点的相关性
Mol Genet Genomics. 2006 Sep;276(3):230-41. doi: 10.1007/s00438-006-0136-6. Epub 2006 Jun 7.

引用本文的文献

1
Most Tibetan weedy barleys originated via recombination between Btr1 and Btr2 in domesticated barley.大多数西藏杂草大麦起源于驯化大麦中 Btr1 和 Btr2 之间的重组。
Plant Commun. 2024 May 13;5(5):100828. doi: 10.1016/j.xplc.2024.100828. Epub 2024 Jan 30.
2
Genome diversity and highland-adaptative variation in Tibet barley landrace population of China.中国西藏青稞地方品种群体的基因组多样性与高原适应性变异
Front Plant Sci. 2023 May 10;14:1189642. doi: 10.3389/fpls.2023.1189642. eCollection 2023.
3
Genome resequencing and transcriptome profiling reveal molecular evidence of tolerance to water deficit in barley.
基因组重测序和转录组谱分析揭示了大麦耐受水分亏缺的分子证据。
J Adv Res. 2023 Jul;49:31-45. doi: 10.1016/j.jare.2022.09.008. Epub 2022 Sep 25.
4
Grain Disarticulation in Wild Wheat and Barley.野生小麦和大麦的籽粒分离。
Plant Cell Physiol. 2022 Nov 22;63(11):1584-1591. doi: 10.1093/pcp/pcac091.
5
Grain dispersal mechanism in cereals arose from a genome duplication followed by changes in spatial expression of genes involved in pollen development.谷物中花粉散布机制的产生源于基因组加倍,随后是参与花粉发育的基因在空间表达上的变化。
Theor Appl Genet. 2022 Apr;135(4):1263-1277. doi: 10.1007/s00122-022-04029-8. Epub 2022 Feb 22.
6
Transcriptome and Metabolite Insights into Domestication Process of Cultivated Barley in China.中国栽培大麦驯化过程的转录组和代谢物洞察
Plants (Basel). 2022 Jan 14;11(2):209. doi: 10.3390/plants11020209.
7
Origin and evolution of qingke barley in Tibet.西藏青稞的起源与演化。
Nat Commun. 2018 Dec 21;9(1):5433. doi: 10.1038/s41467-018-07920-5.