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首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >Complete DNA sequence and characterization of a 330-kb VNTR-rich region on chromosome 6q27 that is commonly deleted in ovarian cancer.
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Complete DNA sequence and characterization of a 330-kb VNTR-rich region on chromosome 6q27 that is commonly deleted in ovarian cancer.

机译:完整的DNA序列和6q27染色体上330kb VNTR富集区域的特征,该区域通常在卵巢癌中缺失。

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We report the complete genomic DNA sequence and the characterization of a 330-kb region on chromosome 6q27 that is often deleted in ovarian cancers. Using computer programs to predict exonic sequences, we isolated four novel genes, HGC6.1-4, as well as the known AF-6 gene. None of the deduced products of the novel genes exhibited significant homology to previously known proteins. We also identified ten microsatellites and 12 different VNTR sequences within the target region. HGC6.3 contained a VNTR within a coding exon, each repeat consisting of 42 nucleotides; the predicted 14-amino-acid consensus unit is MTPTVFSSQHTAGG. At least nine different sizes of this VNTR locus were detected among 20 unrelated DNA samples from caucasians. The polymorphic markers and the transcript map documented here may contribute to identification of novel genes or allelic aberrations associated with the development of ovarian cancers.
机译:我们报告了完整的基因组DNA序列和染色体6q27上一个330 kb区域的特征,该区域通常在卵巢癌中被删除。使用计算机程序预测外显子序列,我们分离了四个新基因HGC6.1-4和已知的AF-6基因。新基因的推导产物均未显示出与先前已知蛋白质的显着同源性。我们还确定了目标区域内的十个微卫星和12个不同的VNTR序列。 HGC6.3在一个编码外显子中包含一个VNTR,每个重复由42个核苷酸组成;预测的14个氨基酸的共有单位为MTPTVFSSQHTAGG。在来自白种人的20个无关DNA样本中,至少检测到9种不同大小的VNTR基因座。此处记录的多态性标记和转录图可能有助于鉴定与卵巢癌发展相关的新基因或等位基因畸变。

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