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iScience. 2025 Mar 27;28(5):112301. doi: 10.1016/j.isci.2025.112301 Q14.62024

Long read genome unravels MHC I genomic architecture, evolution, and diversity loss in Gubernatrix cristata

长读取基因组揭示了Gubernatrix cristata的MHC I基因组架构、进化和多样性丧失 翻译改进

Marisol Domínguez  1, Enrique Celemín  1, Nikolai Gusev  1, Binia De Cahsan  2, Katja Havenstein  1, Bettina Mahler  3, Ralph Tiedemann  1

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作者单位

  • 1 Unit of Evolutionary Biology/Systematic Zoology, Institute for Biochemistry and Biology, University of Potsdam, Potsdam, Germany.
  • 2 Globe Institute, University of Copenhagen, Copenhagen, Denmark.
  • 3 IEGEBA, FCEN-UBA, Pabellón II, Ciudad Universitaria, Ciudad Autónoma de Buenos Aires 1428, Argentina.
  • DOI: 10.1016/j.isci.2025.112301 PMID: 40491960

    摘要 中英对照阅读

    The major histocompatibility complex (MHC) genes are vital for the adaptive immune response in vertebrates and are widely used in conservation genetics to represent adaptive variation. Accurate genotyping of MHC alleles is essential for effective conservation, particularly for endangered species like the yellow cardinal (Gubernatrix cristata). However, the absence of locus-specific primers and the highly repetitive nature of these genes present a technical limitation when using short-read sequencing technologies. We produced the first high-quality long-read reference genome for the yellow cardinal. This genome reveals sustained high genome-wide heterozygosity despite inbreeding, with homozygosity patterns and effective population size estimates indicating a long-term decline. We identified seven genomic MHC-I loci, while amplicon sequencing with non-locus specific primers had not confirmed more than two MHC-I loci. Our study also revealed mismatches in primer binding sites across multiple loci, emphasizing the need for high-quality, long-read genomic data to understand the genomic architecture of MCH and to accurately assess locus specific MHC variation.

    Keywords: Evolutionary biology; Genomics; Ornithology.

    Keywords:long read genome; genomic architecture; evolution; diversity loss

    主要组织相容性复合体(MHC)基因对于脊椎动物的适应性免疫反应至关重要,在保护遗传学中被广泛用于代表适应性变异。准确地对 MHC 基因进行基因分型对于有效的保护工作尤其重要,特别是对于像黄雀(Gubernatrix cristata)这样的濒危物种。然而,在使用短读测序技术时,缺乏位点特异性引物以及这些基因的高度重复特性构成了技术上的限制。我们为黄雀生成了第一个高质量的长读参考基因组。该基因组揭示了尽管存在近亲繁殖,全基因组范围内的杂合性仍然很高,并且同源性模式和有效种群规模估计表明长期呈下降趋势。我们确定了七个 MHC-I 位点,而使用非位点特异性引物进行扩增子测序未能确认超过两个 MHC-I 位点。我们的研究还揭示了多个位点上引物结合位点的不匹配现象,强调了为了理解 MCH 的基因组结构并准确评估特定位点的 MHC 变异,需要高质量、长读取的基因组数据。

    关键词:进化生物学;基因组学;鸟类学

    关键词:长读基因组; 主要组织相容性复合体; 基因组结构; 进化; 多样性丧失

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    期刊名:Iscience

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    ISSN:2589-0042

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    IF/分区:4.6/Q1

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