• 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

基于全基因组水平研究云杉和蒙古栎的适应辐射、历史种群动态及适宜分布区模拟。

Adaptive divergence, historical population dynamics, and simulation of suitable distributions for Picea Meyeri and P. Mongolica at the whole-genome level.

机构信息

Key Laboratory of Forest Ecology and Environment of National Forestry and Grassland Administration, Ecology and Nature Conservation Institute, Chinese Academy of Forestry, Beijing, 100091, China.

Heilongjiang Forestry Research Institute, Harbin, 150080, China.

出版信息

BMC Plant Biol. 2024 May 30;24(1):479. doi: 10.1186/s12870-024-05166-6.

DOI:10.1186/s12870-024-05166-6
PMID:38816690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11137980/
Abstract

The taxonomic classification of Picea meyeri and P. mongolica has long been controversial. To investigate the genetic relatedness, evolutionary history, and population history dynamics of these species, genotyping-by-sequencing (GBS) technology was utilized to acquire whole-genome single nucleotide polymorphism (SNP) markers, which were subsequently used to assess population structure, population dynamics, and adaptive differentiation. Phylogenetic and population structural analyses at the genomic level indicated that although the ancestor of P. mongolica was a hybrid of P. meyeri and P. koraiensis, P. mongolica is an independent Picea species. Additionally, P. mongolica is more closely related to P. meyeri than to P. koraiensis, which is consistent with its geographic distribution. There were up to eight instances of interspecific and intraspecific gene flow between P. meyeri and P. mongolica. The P. meyeri and P. mongolica effective population sizes generally decreased, and Maxent modeling revealed that from the Last Glacial Maximum (LGM) to the present, their habitat areas decreased initially and then increased. However, under future climate scenarios, the habitat areas of both species were projected to decrease, especially under high-emission scenarios, which would place P. mongolica at risk of extinction and in urgent need of protection. Local adaptation has promoted differentiation between P. meyeri and P. mongolica. Genotype‒environment association analysis revealed 96,543 SNPs associated with environmental factors, mainly related to plant adaptations to moisture and temperature. Selective sweeps revealed that the selected genes among P. meyeri, P. mongolica and P. koraiensis are primarily associated in vascular plants with flowering, fruit development, and stress resistance. This research enhances our understanding of Picea species classification and provides a basis for future genetic improvement and species conservation efforts.

摘要

白皮松和樟子松的分类一直存在争议。为了研究这两个物种的遗传关系、进化历史和种群历史动态,本研究利用基因分型测序(GBS)技术获取全基因组单核苷酸多态性(SNP)标记,用于评估种群结构、种群动态和适应性分化。基于基因组水平的系统发育和种群结构分析表明,尽管樟子松的祖先是白皮松和红松的杂种,但它是一个独立的松属物种。此外,樟子松与白皮松的亲缘关系比与红松更为密切,这与它的地理分布一致。在白皮松和樟子松之间存在多达 8 次种间和种内基因流。白皮松和樟子松的有效种群大小普遍减少,Maxent 模型表明,从末次冰期最大值(LGM)到现在,它们的栖息地面积先减少后增加。然而,根据未来气候情景预测,两个物种的栖息地面积都将减少,特别是在高排放情景下,这将使樟子松面临灭绝的风险,急需保护。局部适应促进了白皮松和樟子松的分化。基因型-环境关联分析揭示了 96543 个与环境因素相关的 SNP,主要与植物对水分和温度的适应有关。选择扫描揭示了白皮松、樟子松和红松中被选择的基因主要与开花植物、果实发育和抗逆性有关。本研究增进了我们对松属物种分类的认识,为未来的遗传改良和物种保护工作提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/5b5a0bfb2d96/12870_2024_5166_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/2e96b49bbef2/12870_2024_5166_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/46d8e1770d30/12870_2024_5166_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/12c499d6407c/12870_2024_5166_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/4152aad2182c/12870_2024_5166_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/061d38159e5f/12870_2024_5166_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/7c85caf1009e/12870_2024_5166_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/6a03dbf65904/12870_2024_5166_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/554b264d7076/12870_2024_5166_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/61628775ddad/12870_2024_5166_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/4eb43f8a918d/12870_2024_5166_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/9822767350ad/12870_2024_5166_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/9116335efcaa/12870_2024_5166_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/5b5a0bfb2d96/12870_2024_5166_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/2e96b49bbef2/12870_2024_5166_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/46d8e1770d30/12870_2024_5166_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/12c499d6407c/12870_2024_5166_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/4152aad2182c/12870_2024_5166_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/061d38159e5f/12870_2024_5166_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/7c85caf1009e/12870_2024_5166_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/6a03dbf65904/12870_2024_5166_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/554b264d7076/12870_2024_5166_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/61628775ddad/12870_2024_5166_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/4eb43f8a918d/12870_2024_5166_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/9822767350ad/12870_2024_5166_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/9116335efcaa/12870_2024_5166_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b8/11137980/5b5a0bfb2d96/12870_2024_5166_Fig13_HTML.jpg

相似文献

1
Adaptive divergence, historical population dynamics, and simulation of suitable distributions for Picea Meyeri and P. Mongolica at the whole-genome level.基于全基因组水平研究云杉和蒙古栎的适应辐射、历史种群动态及适宜分布区模拟。
BMC Plant Biol. 2024 May 30;24(1):479. doi: 10.1186/s12870-024-05166-6.
2
Species divergence and environmental adaptation of complex at the whole genome level.全基因组水平上复合体的物种分化与环境适应性
Ecol Evol. 2024 Aug 6;14(8):e70126. doi: 10.1002/ece3.70126. eCollection 2024 Aug.
3
Interspecific Gene Flow and Selective Sweeps in , and .种间基因流动以及[具体物种1]、[具体物种2]和[具体物种3]中的选择性清除
Plants (Basel). 2022 Nov 6;11(21):2993. doi: 10.3390/plants11212993.
4
Population Structure, Genetic Diversity and Candidate Genes for the Adaptation to Environmental Stress in .群体结构、遗传多样性以及适应环境胁迫的候选基因 于……中
Plants (Basel). 2023 Mar 10;12(6):1266. doi: 10.3390/plants12061266.
5
Transcriptome-based analyses of adaptive divergence between two closely related spruce species on the Qinghai-Tibet plateau and adjacent regions.基于转录组对青藏高原及邻近地区两种近缘云杉物种适应性分化的分析。
Mol Ecol. 2023 Jan;32(2):476-491. doi: 10.1111/mec.16758. Epub 2022 Nov 16.
6
Tracking the progression of speciation: variable patterns of introgression across the genome provide insights on the species delimitation between progenitor-derivative spruces (Picea mariana × P. rubens).追踪物种形成的进程:全基因组渗入的可变模式为探讨祖先衍生云杉(黑云杉×红云杉)之间的物种界定提供了见解。
Mol Ecol. 2015 Oct;24(20):5229-47. doi: 10.1111/mec.13377. Epub 2015 Oct 12.
7
Scanning the genome for gene SNPs related to climate adaptation and estimating selection at the molecular level in boreal black spruce.扫描基因组中与气候适应相关的基因 SNPs,并在分子水平估计北方黑云杉的选择。
Mol Ecol. 2011 Apr;20(8):1702-16. doi: 10.1111/j.1365-294X.2011.05045.x. Epub 2011 Mar 7.
8
Scanning the genome for gene single nucleotide polymorphisms involved in adaptive population differentiation in white spruce.扫描白云杉基因组中与适应性种群分化相关的基因单核苷酸多态性。
Mol Ecol. 2008 Aug;17(16):3599-613. doi: 10.1111/j.1365-294X.2008.03840.x. Epub 2008 Jul 3.
9
Development of a highly efficient 50K single nucleotide polymorphism genotyping array for the large and complex genome of Norway spruce (Picea abies L. Karst) by whole genome resequencing and its transferability to other spruce species.利用全基因组重测序开发高效的 50K 单核苷酸多态性基因分型芯片用于挪威云杉(Picea abies L. Karst)这个庞大而复杂的基因组及其向其他云杉物种的可转移性。
Mol Ecol Resour. 2021 Apr;21(3):880-896. doi: 10.1111/1755-0998.13292. Epub 2020 Dec 2.
10
Parallel and lineage-specific molecular adaptation to climate in boreal black spruce.北方黑云杉的气候适应的平行和谱系特异性分子机制。
Mol Ecol. 2012 Sep;21(17):4270-86. doi: 10.1111/j.1365-294X.2012.05691.x. Epub 2012 Jul 16.

引用本文的文献

1
A complex interplay of genetic introgression and local adaptation during the evolutionary history of three closely related spruce species.在三种亲缘关系密切的云杉物种的进化历史中,基因渐渗与局部适应之间存在复杂的相互作用。
Plant Divers. 2025 May 15;47(4):620-632. doi: 10.1016/j.pld.2025.04.007. eCollection 2025 Jul.

本文引用的文献

1
Identification of Brassica rapa BrEBF1 homologs and their characterization in cold signaling.鉴定芸薹属 BrEBF1 同源物及其在低温信号转导中的特征。
J Plant Physiol. 2023 Sep;288:154076. doi: 10.1016/j.jplph.2023.154076. Epub 2023 Aug 25.
2
Characterization of SEC14 family in wheat and the function of TaSEC14-7B in salt stress tolerance.小麦 SEC14 家族的鉴定和 TaSEC14-7B 基因在耐盐性中的功能。
Plant Physiol Biochem. 2023 Sep;202:107926. doi: 10.1016/j.plaphy.2023.107926. Epub 2023 Aug 2.
3
Population Structure, Genetic Diversity and Candidate Genes for the Adaptation to Environmental Stress in .
群体结构、遗传多样性以及适应环境胁迫的候选基因 于……中
Plants (Basel). 2023 Mar 10;12(6):1266. doi: 10.3390/plants12061266.
4
Selective sweeps linked to the colonization of novel habitats and climatic changes in a wild tomato species.与一种野生番茄物种的新栖息地定殖和气候变化相关的选择性清除。
New Phytol. 2023 Mar;237(5):1908-1921. doi: 10.1111/nph.18634. Epub 2022 Dec 15.
5
Interspecific Gene Flow and Selective Sweeps in , and .种间基因流动以及[具体物种1]、[具体物种2]和[具体物种3]中的选择性清除
Plants (Basel). 2022 Nov 6;11(21):2993. doi: 10.3390/plants11212993.
6
Transcriptome-based analyses of adaptive divergence between two closely related spruce species on the Qinghai-Tibet plateau and adjacent regions.基于转录组对青藏高原及邻近地区两种近缘云杉物种适应性分化的分析。
Mol Ecol. 2023 Jan;32(2):476-491. doi: 10.1111/mec.16758. Epub 2022 Nov 16.
7
Genome-wide identification and characterization of AP2/ERF gene superfamily during flower development in Actinidia eriantha.在软枣猕猴桃花发育过程中全基因组鉴定和分析 AP2/ERF 基因超家族。
BMC Genomics. 2022 Sep 13;23(1):650. doi: 10.1186/s12864-022-08871-4.
8
Genomic divergence of Stellera chamaejasme through local selection across the Qinghai-Tibet plateau and northern China.青藏高原和中国北方地区通过局部选择导致斜茎獐牙菜的基因组分化。
Mol Ecol. 2022 Sep;31(18):4782-4796. doi: 10.1111/mec.16622. Epub 2022 Aug 3.
9
MYB2 Is Important for Tapetal PCD and Pollen Development by Directly Activating Protease Expression in .MYB2 通过直接激活. 中的蛋白酶表达对绒毡层 PCD 和花粉发育很重要。
Int J Mol Sci. 2022 Mar 24;23(7):3563. doi: 10.3390/ijms23073563.
10
Species divergence with gene flow and hybrid speciation on the Qinghai-Tibet Plateau.青藏高原上的基因流物种分化和杂种形成。
New Phytol. 2022 Apr;234(2):392-404. doi: 10.1111/nph.17956. Epub 2022 Jan 30.