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The mole genome reveals regulatory rearrangements associated with adaptive intersexuality

机译:摩尔基因组揭示了与适应性三分性相关的调节重排

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摘要

Linking genomic variation to phenotypical traits remains a major challenge in evolutionary genetics. In this study, we use phylogenomic strategies to investigate a distinctive trait among mammals: the development of masculinizing ovotestes in female moles. By combining a chromosome-scale genome assembly of the Iberian mole, Talpa occidentalis, with transcriptomic, epigenetic, and chromatin interaction datasets, we identify rearrangements altering the regulatory landscape of genes with distinct gonadal expression patterns. These include a tandem triplication involving CYP17A1, a gene controlling androgen synthesis, and an intrachromosomal inversion involving the pro-testicular growth factor gene FGF9, which is heterochronically expressed in mole ovotestes. Transgenic mice with a knock-in mole CYP17A1 enhancer or overexpressing FGF9 showed phenotypes recapitulating mole sexual features. Our results highlight how integrative genomic approaches can reveal the phenotypic impact of noncoding sequence changes.
机译:将基因组变异与表型特性联系起来仍然是进化遗传学的主要挑战。在这项研究中,我们使用文学组织策略来调查哺乳动物中的独特性状:雌性痣中阳性化卵囊的发展。通过组合Iberian Mole的染色体型基因组组件,Talpa occidentalis与转录组,表观遗传和染色质相互作用数据集,我们识别重新排列,改变具有不同性腺表达模式的基因的调节景观。这些包括涉及CYP17A1的串联三次,该基因控制雄激素合成,以及涉及亲睾丸生长因子基因FGF9的血管囊瘤复位,其在摩尔OVOTESTES中异相表示。具有敲入摩尔CYP17A1增强剂或过表达FGF9的转基因小鼠表现出重新制备摩尔性特征的表型。我们的结果强调了综合基因组方法如何揭示非编码序列变化的表型影响。

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  • 来源
    《Science》 |2020年第6513期|208-214|共7页
  • 作者单位

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany|Charite Univ Med Berlin Inst Med & Human Genet Berlin Germany;

    Max Planck Inst Mol Genet Dept Computat Mol Biol Berlin Germany;

    Univ Konstanz Dept Biol Zool & Evolutionary Biol D-78457 Constance Germany;

    Univ Konstanz Dept Biol Zool & Evolutionary Biol D-78457 Constance Germany;

    Univ Vienna Dept Mol Evolut & Dev A-1090 Vienna Austria;

    Leibniz Inst Freshwater Ecol & Inland Fisheries Dept Ecophysiol & Aquaculture Berlin Germany;

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany|Charite Univ Med Berlin Inst Med & Human Genet Berlin Germany;

    Max Planck Inst Mol Genet Dept Computat Mol Biol Berlin Germany;

    Max Planck Inst Mol Genet Dept Computat Mol Biol Berlin Germany;

    Max Planck Inst Mol Genet Dept Computat Mol Biol Berlin Germany;

    Max Planck Inst Mol Genet Dept Computat Mol Biol Berlin Germany;

    Max Planck Inst Mol Genet Dept Computat Mol Biol Berlin Germany;

    Justus Liebig Univ Div Paediat Endocrinol & Diabetol Steroid Res & Mass Spectrometry Unit Ctr Child & Adolescent Med Lab Translat Hormone A Giessen Germany;

    Justus Liebig Univ Div Paediat Endocrinol & Diabetol Steroid Res & Mass Spectrometry Unit Ctr Child & Adolescent Med Lab Translat Hormone A Giessen Germany;

    Max Planck Inst Annual Behav Dept Migrat & Immunoecol Radolfzell am Bodensee Germany|Univ Konstanz Dept Biol Constance Germany;

    Univ Granada Dept Genet Granada Spain|Univ Granada Inst Biotecnol Ctr Invest Biomed Granada Spain;

    Univ Granada Dept Genet Granada Spain|Univ Granada Inst Biotecnol Ctr Invest Biomed Granada Spain;

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany|Charite Univ Med Berlin Inst Med & Human Genet Berlin Germany;

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany;

    Lawrence Berkeley Natl Lab Environm Genom & Syst Biol Div Berkeley CA 94720 USA|Univ Bern Dept BioMed Res DBMR CH-3008 Bern Switzerland;

    Max Planck Inst Mol Cell Biol & Genet D-01307 Dresden Germany|Max Planck Inst Phys Komplexer Syst D-01187 Dresden Germany|Ctr Syst Biol Dresden D-01307 Dresden Germany;

    Max Planck Inst Mol Genet Dept Dev Genet Transgen Unit Berlin Germany;

    Lawrence Berkeley Natl Lab Environm Genom & Syst Biol Div Berkeley CA 94720 USA|US DOE Joint Genome Inst Berkeley CA 94720 USA|Univ Calif Merced Sch Nat Sci Merced CA 95343 USA;

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany;

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany|Charite Univ Med Berlin Inst Med & Human Genet Berlin Germany|Charite Univ Med Berlin Berlin Brandenburg Ctr Regenerat Therapies BCRT Berlin Germany;

    Max Planck Inst Mol Genet RG Dev & Dis Berlin Germany|Charite Univ Med Berlin Inst Med & Human Genet Berlin Germany|Charite Univ Med Berlin Berlin Brandenburg Ctr Regenerat Therapies BCRT Berlin Germany|Max Delbruck Ctr Mol Med Berlin Inst Med Syst Biol Epigenet & Sex Dev Grp Berlin Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 22:15:12

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