Allikmets R L, Kashuba V I, Pettersson B, Gizatullin R, Lebedeva T, Kholodnyuk I D, Bannikov V M, Petrov N, Zakharyev V M, Winberg G
Laboratory of Viral Carcinogenesis, National Cancer Institute, FCRDC, Frederick, Maryland 21702.
Genomics. 1994 Jan 15;19(2):303-9. doi: 10.1006/geno.1994.1062.
To study the connection among NotI linking clones, CpG islands, and genes, the sequence surrounding 143 NotI sites was determined. These NotI linking clones were isolated from human chromosome 3-specific libraries and contain an average C + G content of 65%. These clones represent sequence-tagged sites that can be positioned onto chromosome maps and used for generating a long-range NotI map of the human genome. A majority (about 90%) of these clones contain transcribed sequences, as detected by Northern blot hybridization, providing an efficient link between physical and functional (genetic) maps. The GenBank nucleotide database was searched with sequences from these NotI linking clones. For many clones, homology was found to human and other vertebrate genes. About 20 clones contained various repeats in their sequences and may represent microsatellite loci. Most of these NotI linking clones therefore represent evolutionarily conserved DNA fragments and also can be used for comparative genome mapping of other mammalian species. In addition, approximately 20% of all sequenced human CpG island-containing genes and more than 12% of all well-characterized human genes were found to possess NotI restriction sites. This is at least 2-5 times more than has been previously estimated and suggests that NotI sites have a much stronger association with genes.
为了研究NotI连接克隆、CpG岛和基因之间的联系,我们测定了143个NotI位点周围的序列。这些NotI连接克隆是从人3号染色体特异性文库中分离出来的,平均C+G含量为65%。这些克隆代表了序列标签位点,可定位到染色体图谱上,并用于构建人类基因组的长程NotI图谱。通过Northern印迹杂交检测发现,这些克隆中的大多数(约90%)含有转录序列,从而在物理图谱和功能(遗传)图谱之间建立了有效联系。我们用这些NotI连接克隆的序列搜索了GenBank核苷酸数据库。对于许多克隆,发现它们与人类及其他脊椎动物基因具有同源性。约20个克隆的序列中含有各种重复序列,可能代表微卫星位点。因此,这些NotI连接克隆中的大多数代表了进化上保守的DNA片段,也可用于其他哺乳动物物种的比较基因组图谱绘制。此外,发现所有已测序的含人类CpG岛基因中约20%以及所有已充分表征的人类基因中超过12%都具有NotI限制性位点。这至少比先前估计的多2至5倍,表明NotI位点与基因的关联要强得多。