Zentrum für Medizinische Strukturbiologie, Institut für Biologie, Universität Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Germany.
Chromosome Res. 2013 Aug;21(5):491-505. doi: 10.1007/s10577-013-9376-6. Epub 2013 Aug 15.
Y and W chromosomes have mostly been excluded from whole genome sequencing projects. Due to the high amount of repetitive sequences they are 'difficult' to assemble and therefore need special treatment in the form of, e.g. adapted assembly programs, a range of different libraries, and accurate maps, if possible. A minimum requirement for these approaches is pure template DNA. We therefore microdissected the W chromatin of highly polyploid cells from the flour moth, Ephestia kuehniella, and used Roche/454 and Sanger sequencing to generate 72.6 Mbp of DNA sequence. Nominal coverage was 4.3× of the 16.7 Mbp of W chromosomal DNA. We used these data to assess the genetic content of the W chromosome. This approach allowed us to determine constituent families of transposable elements, microsatellites, and recent insertion sites of mitochondrial DNA. However, no conventional protein-coding gene has yet been found. The sequence collection is a rich source for the definition of W-specific PCR markers and the reconstruction of W chromosome loci, as a step towards full reconstruction of the chromosome.
Y 和 W 染色体在全基因组测序项目中大多被排除在外。由于它们含有大量重复序列,因此“难以”组装,因此需要特殊处理,例如使用适应性组装程序、一系列不同的文库和尽可能准确的图谱。这些方法的最低要求是纯模板 DNA。因此,我们从小粉纹夜蛾(Ephestia kuehniella)的高度多倍体细胞中微切割 W 染色质,并使用罗氏/454 和 Sanger 测序生成 72.6 Mbp 的 DNA 序列。名义覆盖率为 16.7 Mbp W 染色体 DNA 的 4.3×。我们使用这些数据来评估 W 染色体的遗传内容。这种方法使我们能够确定转座元件、微卫星和线粒体 DNA 最近插入位点的组成家族。然而,尚未发现常规的蛋白质编码基因。该序列集是定义 W 特异性 PCR 标记和重建 W 染色体基因座的丰富资源,是全面重建染色体的一步。