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High-throughput sequencing of a single chromosome: a moth W chromosome

机译:单条染色体的高通量测序:蛾W染色体

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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.
机译:Y和W染色体大部分已被排除在全基因组测序项目之外。由于重复序列数量很多,它们很难“组装”,因此需要特殊处理,例如修改后的汇编程序,一系列不同的库以及准确的地图(如果可能)。这些方法的最低要求是纯模板DNA。因此,我们从the蛾(Ephestia kuehniella)中显微切割了高度多倍体细胞的W染色质,并使用Roche / 454和Sanger测序产生了72.6 Mbp的DNA序列。标称覆盖率为W染色体DNA 16.7 Mbp的4.3倍。我们使用这些数据来评估W染色体的遗传含量。这种方法使我们能够确定转座因子,微卫星和线粒体DNA最近插入位点的组成族。但是,尚未发现常规的蛋白质编码基因。序列收集为W特异性PCR标记的定义和W染色体基因座的重建提供了丰富的资源,是朝着染色体的完全重建迈出的一步。

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