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1
Substantial Heritable Variation in Recombination Rate on Multiple Scales in Honeybees and Bumblebees.在多个尺度上,蜜蜂和熊蜂的重组率存在大量的可遗传性变异。
Genetics. 2019 Aug;212(4):1101-1119. doi: 10.1534/genetics.119.302008. Epub 2019 May 31.
2
Extreme recombination frequencies shape genome variation and evolution in the honeybee, Apis mellifera.极高的重组频率塑造了蜜蜂(西方蜜蜂)的基因组变异和进化。
PLoS Genet. 2015 Apr 22;11(4):e1005189. doi: 10.1371/journal.pgen.1005189. eCollection 2015 Apr.
3
Direct Determination of the Mutation Rate in the Bumblebee Reveals Evidence for Weak Recombination-Associated Mutation and an Approximate Rate Constancy in Insects.对大黄蜂突变率的直接测定揭示了弱重组相关突变的证据以及昆虫中近似的速率恒定性。
Mol Biol Evol. 2017 Jan;34(1):119-130. doi: 10.1093/molbev/msw226. Epub 2016 Oct 20.
4
Extreme Differences in Recombination Rate between the Genomes of a Solitary and a Social Bee.独居蜂和社会性蜂基因组中重组率的极端差异。
Mol Biol Evol. 2019 Oct 1;36(10):2277-2291. doi: 10.1093/molbev/msz130.
5
The genomes of two key bumblebee species with primitive eusocial organization.具有原始群居组织的两种关键熊蜂物种的基因组。
Genome Biol. 2015 Apr 24;16(1):76. doi: 10.1186/s13059-015-0623-3.
6
A depauperate immune repertoire precedes evolution of sociality in bees.蜜蜂社会性进化之前存在免疫库衰退现象。
Genome Biol. 2015 Apr 24;16(1):83. doi: 10.1186/s13059-015-0628-y.
7
Causes and consequences of crossing-over evidenced via a high-resolution recombinational landscape of the honey bee.通过蜜蜂的高分辨率重组图谱揭示的交叉互换的原因及后果
Genome Biol. 2015 Jan 2;16(1):15. doi: 10.1186/s13059-014-0566-0.
8
Fine scale analysis of crossover and non-crossover and detection of recombination sequence motifs in the honeybee (Apis mellifera).对蜜蜂(Apis mellifera)中的交叉和非交叉以及重组序列基序的精细分析。
PLoS One. 2012;7(5):e36229. doi: 10.1371/journal.pone.0036229. Epub 2012 May 2.
9
Comparative linkage mapping suggests a high recombination rate in all honeybees.比较连锁图谱表明所有蜜蜂的重组率都很高。
J Hered. 2010 Mar-Apr;101 Suppl 1:S118-26. doi: 10.1093/jhered/esq002. Epub 2010 Mar 8.
10
Gene expression during larval caste determination and differentiation in intermediately eusocial bumblebees, and a comparative analysis with advanced eusocial honeybees.中等群居性熊蜂幼虫级型决定和分化过程中的基因表达,以及与高等群居性蜜蜂的比较分析。
Mol Ecol. 2021 Feb;30(3):718-735. doi: 10.1111/mec.15752. Epub 2021 Jan 7.

引用本文的文献

1
Mixed Outcomes in Recombination Rates After Domestication: Revisiting Theory and Data.驯化后重组率的混合结果:重新审视理论与数据
Mol Ecol. 2025 Apr 24:e17773. doi: 10.1111/mec.17773.
2
Unexpectedly low recombination rates and presence of hotspots in termite genomes.白蚁基因组中意外低的重组率和热点的存在。
Genome Res. 2025 May 2;35(5):1124-1137. doi: 10.1101/gr.279180.124.
3
Inferring Long-Term and Short-Term Determinants of Genetic Diversity in Honey Bees: Beekeeping Impact and Conservation Strategies.推断蜜蜂遗传多样性的长期和短期决定因素:养蜂的影响及保护策略。
Mol Biol Evol. 2024 Dec 6;41(12). doi: 10.1093/molbev/msae249.
4
Alternative double strand break repair pathways shape the evolution of high recombination in the honey bee, Apis mellifera.替代双链断裂修复途径塑造了蜜蜂(西方蜜蜂)高重组率的进化。
Insect Mol Biol. 2025 Feb;34(1):185-202. doi: 10.1111/imb.12961. Epub 2024 Sep 19.
5
Understanding the Genetic Basis of Variation in Meiotic Recombination: Past, Present, and Future.理解减数分裂重组中变异的遗传基础:过去、现在和未来。
Mol Biol Evol. 2024 Jul 3;41(7). doi: 10.1093/molbev/msae112.
6
Base Composition, Codon Usage, and Patterns of Gene Sequence Evolution in Butterflies.蝴蝶的碱基组成、密码子使用和基因序列进化模式。
Genome Biol Evol. 2023 Aug 1;15(8). doi: 10.1093/gbe/evad150.
7
Modeling Recombination Rate as a Quantitative Trait Reveals New Insight into Selection in Humans.将重组率建模为一种数量性状,为人类选择提供了新的见解。
Genome Biol Evol. 2023 Aug 1;15(8). doi: 10.1093/gbe/evad132.
8
AmelHap: Leveraging drone whole-genome sequence data to create a honey bee HapMap.AmelHap:利用无人机全基因组序列数据创建蜜蜂 HapMap。
Sci Data. 2023 Apr 10;10(1):198. doi: 10.1038/s41597-023-02097-z.
9
Complex population structure and haplotype patterns in the Western European honey bee from sequencing a large panel of haploid drones.从大量单倍体雄蜂的测序结果来看,西欧蜜蜂具有复杂的种群结构和单倍型模式。
Mol Ecol Resour. 2022 Nov;22(8):3068-3086. doi: 10.1111/1755-0998.13665. Epub 2022 Jun 27.
10
Fragile, unfaithful and persistent Ys-on how meiosis can shape sex chromosome evolution.脆弱、不忠且持久的 Y 染色体——减数分裂如何塑造性染色体进化。
Heredity (Edinb). 2022 Jul;129(1):22-30. doi: 10.1038/s41437-022-00532-2. Epub 2022 Apr 22.

本文引用的文献

1
Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): infestation with spp. (varroosis).在《动物卫生法》(欧盟第2016/429号条例)框架内对动物疾病进行列名和分类的评估:感染 spp.(蜂螨病)。
EFSA J. 2017 Oct 6;15(10):e04997. doi: 10.2903/j.efsa.2017.4997. eCollection 2017 Oct.
2
A hybrid de novo genome assembly of the honeybee, Apis mellifera, with chromosome-length scaffolds.具有染色体级别的蜜蜂(Apis mellifera)从头杂交基因组组装。
BMC Genomics. 2019 Apr 8;20(1):275. doi: 10.1186/s12864-019-5642-0.
3
Field-level clothianidin exposure affects bumblebees but generally not their pathogens.田间水平的噻虫啉暴露会影响熊蜂,但通常不会影响其病原体。
Nat Commun. 2018 Dec 21;9(1):5446. doi: 10.1038/s41467-018-07914-3.
4
A Genomic Region Containing and Is Associated with Individual Recombination Rate Variation in a Wild Population of Red Deer ().一个包含[具体内容未给出]的基因组区域与马鹿([具体物种名未给出])野生种群中个体重组率变异相关。
G3 (Bethesda). 2018 Jul 2;8(7):2265-2276. doi: 10.1534/g3.118.200063.
5
Meiotic Recombination: Mixing It Up in Plants.减数分裂重组:植物中的混合现象。
Annu Rev Plant Biol. 2018 Apr 29;69:577-609. doi: 10.1146/annurev-arplant-042817-040431. Epub 2018 Feb 28.
6
lme4qtl: linear mixed models with flexible covariance structure for genetic studies of related individuals.lme4qtl:用于相关个体遗传研究的具有灵活协方差结构的线性混合效应模型。
BMC Bioinformatics. 2018 Feb 27;19(1):68. doi: 10.1186/s12859-018-2057-x.
7
Are the effects of elevated temperature on meiotic recombination and thermotolerance linked via the axis and synaptonemal complex?温度升高对减数分裂重组和耐热性的影响是否通过轴和联会复合体相关联?
Philos Trans R Soc Lond B Biol Sci. 2017 Dec 19;372(1736). doi: 10.1098/rstb.2016.0470.
8
Variation in recombination frequency and distribution across eukaryotes: patterns and processes.真核生物中重组频率和分布的变化:模式和过程。
Philos Trans R Soc Lond B Biol Sci. 2017 Dec 19;372(1736). doi: 10.1098/rstb.2016.0455.
9
Evidence of reduced recombination rate in human regulatory domains.人类调控区重组率降低的证据。
Genome Biol. 2017 Oct 20;18(1):193. doi: 10.1186/s13059-017-1308-x.
10
Whole-genome patterns of linkage disequilibrium across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds.across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds.\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
Mol Ecol. 2017 Aug;26(16):4158-4172. doi: 10.1111/mec.14197. Epub 2017 Jul 5.

在多个尺度上,蜜蜂和熊蜂的重组率存在大量的可遗传性变异。

Substantial Heritable Variation in Recombination Rate on Multiple Scales in Honeybees and Bumblebees.

机构信息

Department of Evolutionary Biology, Evolutionary Biology Centre (EBC), Uppsala University, 752 36, Sweden.

Department of Animal and Plant Sciences, University of Sheffield, S10 2TN, United Kingdom.

出版信息

Genetics. 2019 Aug;212(4):1101-1119. doi: 10.1534/genetics.119.302008. Epub 2019 May 31.

DOI:10.1534/genetics.119.302008
PMID:31152071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6707477/
Abstract

Meiotic recombination shuffles genetic variation and promotes correct segregation of chromosomes. Rates of recombination vary on several scales, both within genomes and between individuals, and this variation is affected by both genetic and environmental factors. Social insects have extremely high rates of recombination, although the evolutionary causes of this are not known. Here, we estimate rates of crossovers and gene conversions in 22 colonies of the honeybee, , and 9 colonies of the bumblebee, , using direct sequencing of 299 haploid drone offspring. We confirm that both species have extremely elevated crossover rates, with higher rates measured in the highly eusocial honeybee than the primitively social bumblebee. There are also significant differences in recombination rate between subspecies of honeybee. There is substantial variation in genome-wide recombination rate between individuals of both and and the distribution of these rates overlap between species. A large proportion of interindividual variation in recombination rate is heritable, which indicates the presence of variation in -acting factors that influence recombination genome-wide. We infer that levels of crossover interference are significantly lower in honeybees compared to bumblebees, which may be one mechanism that contributes to higher recombination rates in honeybees. We also find a significant increase in recombination rate with distance from the centromere, mirrored by methylation differences. We detect a strong transmission bias due to GC-biased gene conversion associated with noncrossover gene conversions. Our results shed light on the mechanistic causes of extreme rates of recombination in social insects and the genetic architecture of recombination rate variation.

摘要

减数分裂重组打乱了遗传变异,并促进了染色体的正确分离。重组率在多个尺度上变化,包括在基因组内和个体之间,并且这种变化受到遗传和环境因素的影响。社会性昆虫具有极高的重组率,尽管其进化原因尚不清楚。在这里,我们使用 299 个单倍体雄蜂后代的直接测序,估计了 22 个蜜蜂( )和 9 个熊蜂( )殖民地的交叉和基因转换率。我们证实,这两个物种的交叉率都非常高,高度社会性的蜜蜂的交叉率高于原始社会性的熊蜂。蜜蜂亚种之间的重组率也存在显著差异。和 个体之间的全基因组重组率存在很大差异,并且这些速率在物种之间重叠。两种物种的个体之间重组率的大量个体间变异是可遗传的,这表明存在影响全基因组重组的 作用因素的变异。我们推断,与熊蜂相比,蜜蜂中的交叉干扰水平明显较低,这可能是导致蜜蜂重组率较高的一种机制。我们还发现,随着离着丝粒距离的增加,重组率显著增加,这与甲基化差异相呼应。我们检测到由于非交叉基因转换相关的 GC 偏向性基因转换而导致的强烈的传递偏向。我们的结果阐明了社会性昆虫中极端重组率的机制原因以及重组率变化的遗传结构。