Institut de Biologia Evolutiva, (CSIC-Universitat Pompeu Fabra), PRBB, Doctor Aiguader 88, Barcelona, Catalonia, 08003, Spain.
Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Carrer del Doctor Aiguader 88, PRBB Building, Barcelona, 08003, Spain.
Nat Commun. 2019 Jan 2;10(1):4. doi: 10.1038/s41467-018-07885-5.
Mammalian Y chromosomes are often neglected from genomic analysis. Due to their inherent assembly difficulties, high repeat content, and large ampliconic regions, only a handful of species have their Y chromosome properly characterized. To date, just a single human reference quality Y chromosome, of European ancestry, is available due to a lack of accessible methodology. To facilitate the assembly of such complicated genomic territory, we developed a novel strategy to sequence native, unamplified flow sorted DNA on a MinION nanopore sequencing device. Our approach yields a highly continuous assembly of the first human Y chromosome of African origin. It constitutes a significant improvement over comparable previous methods, increasing continuity by more than 800%. Sequencing native DNA also allows to take advantage of the nanopore signal data to detect epigenetic modifications in situ. This approach is in theory generalizable to any species simplifying the assembly of extremely large and repetitive genomes.
哺乳动物的 Y 染色体在基因组分析中经常被忽视。由于其固有的组装困难、高重复含量和大的扩增区域,只有少数物种的 Y 染色体得到了适当的描述。迄今为止,由于缺乏可访问的方法,只有一个具有欧洲血统的人类参考质量的 Y 染色体可用。为了促进这种复杂基因组区域的组装,我们开发了一种新的策略,即在 MinION 纳米孔测序设备上对天然、未扩增的流式分选 DNA 进行测序。我们的方法产生了第一个来自非洲的人类 Y 染色体的高度连续组装。与以前类似的方法相比,它的连续性提高了 800%以上。对天然 DNA 进行测序还可以利用纳米孔信号数据来检测原位的表观遗传修饰。这种方法在理论上可以推广到任何物种,简化了极其庞大和重复的基因组的组装。