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首页> 外文期刊>Comparative and functional genomics >A 4 Mb high resolution BAC contig on bovine chromosome 1q12 and comparative analysis with human chromosome 21q22
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A 4 Mb high resolution BAC contig on bovine chromosome 1q12 and comparative analysis with human chromosome 21q22

机译:牛染色体1q12上的4 Mb高分辨率BAC重叠群与人染色体21q22的比较分析

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The bovine RPCI-42 BAC library was screened to construct a sequence-ready 4 Mb single contig of 92 BAC clones on BTA 1q12. The contig covers the region between the genes KRTAP8P1 and CLIC6. This genomic segment in cattle is of special interest as it contains the dominant gene responsible for the hornless or polled phenotype in cattle. The construction of the BAC contig was initiated by screening the bovine BAC library with heterologous cDNA probes derived from 12 human genes of the syntenic region on HSA 21q22. Contig building was facilitated by BAC end sequencing and chromosome walking. During the construction of the contig, 165 BAC end sequences and 109 single-copy STS markers were generated. For comparative mapping of 25 HSA 21q22 genes, genomic PCR primers were designed from bovine EST sequences and the gene-associated STSs mapped on the contig. Furthermore, bovine BAC end sequence comparisons against the human genome sequence revealed significant matches to HSA 21q22 and allowed the in silico mapping of two new genes in cattle. In total, 31 orthologues of human genes located on HSA 21q22 were directly mapped within the bovine BAC contig, of which 16 genes have been cloned and mapped for the first time in cattle. In contrast to the existing comparative bovine-human RH maps of this region, these results provide a better alignment and reveal a completely conserved gene order in this 4 Mb segment between cattle, human and mouse. The mapping of known polled linked BTA 1q12 microsatellite markers allowed the integration of the physical contig map with existing linkage maps of this region and also determined the exact order of these markers for the first time. Our physical map and transcript map may be useful for positional cloning of the putative polled gene in cattle. The nucleotide sequence data reported in this paper have been submitted to EMBL and have been assigned Accession Numbers AJ698510-AJ698674.
机译:筛选牛RPCI-42 BAC文库以在BTA 1q12上构建92个BAC克隆的序列就绪4 Mb单重叠群。重叠群覆盖基因KRTAP8P1和CLIC6之间的区域。牛的这一基因组片段特别受关注,因为它包含负责牛无角或轮询表型的显性基因。 BAC重叠群的构建是通过用源自HSA 21q22上同义区域的12个人类基因的异源cDNA探针筛选牛BAC文库来启动的。 BAC末端测序和染色体步移促进了重叠群的构建。在重叠群的构建过程中,产生了165个BAC末端序列和109个单拷贝STS标记。为了比较地绘制25个HSA 21q22基因,从牛EST序列设计基因组PCR引物,并将与基因相关的STS定位在重叠群上。此外,牛BAC末端序列与人基因组序列的比较显示出与HSA 21q22的显着匹配,并允许对牛中的两个新基因进行计算机绘图。总共,位于HSA 21q22上的31个人类基因的直向同源物被直接定位在牛BAC重叠群中,其中16个基因已被克隆并首次在牛中定位。与该区域现有的比较牛-人RH图相比,这些结果提供了更好的比对,并揭示了牛,人和小鼠之间4 Mb区段中完全保守的基因顺序。已知的轮询链接BTA 1q12微卫星标记的作图可以将物理重叠群图与该区域的现有链接图进行整合,并首次确定这些标记的确切顺序。我们的物理图谱和转录本图谱可能对在牛中推定的轮询基因的位置克隆有用。本文报道的核苷酸序列数据已提交给EMBL,并获得了登录号AJ698510-AJ698674。

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