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A Human Genomic Library Enriched in Transcriptionally Active Sequences (aDNA Library)

机译:富含转录活性序列的人类基因组文库(aDNA文库)

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摘要

Core histone hyperacetylation, in particular of H4, is concentrated in the promoter–upstream regions of active genes and in certain cases is locuswide. Antibodies to hyperacetylated H4 were used to immunoprecipitate dinucleosomal chromatin derived from K562 human erythroleukemic cells by micrococcal nuclease digestion. The extracted DNA was made into a genomic library and was expected to contain sequences from genes active in K562 cells (an active, ‘aDNA’ library). Clones (180) were randomly selected from the library; 24 of 103 tested (23%) contained highly repeated sequences, as determined by their hybridization to total genomic DNA, and were not analyzed further. An additional 10 clones (6%) were shown to contain no insert DNA. The remaining 146 were sequenced and compared with the nucleic acid databases and in all six frames to the protein databases: Sixeen clones could be assigned to known genes, the majority of which (12) were tissue specific. All but 2 of these 16 corresponded to segments 5′ of the coding sequences, as expected if H4 acetylation is concentrated at promoter regions. Thirty-three clones (23%) displayed high sequence identity to cDNAs in the expressed sequence tag database (dbEST). Northern blots and reverse transcription (RT)—PCR were used to determine the proportion of clones representing sequences expressed in K562 cells: Although only 1 of 34 tested clones showed a band in Northern hybridization, RT–PCR demonstrated that at least 12 of 40 tested clones (30%) were present in the mRNA population. Because a further 8 of these 40 clones were identified as gene fragments by database sequence comparisons, it follows that about half of this subset of 40 clones is derived from genes. The aDNA library is thus very gene rich and not skewed toward the most highly expressed sequences, as in mRNA libraries. The aDNA library is also rich in promoters and could be a valuable source of such sequences, particularly those that lack CpG islands or other features that allow their specific selection.
机译:核心组蛋白的超乙酰化,尤其是H4的超乙酰化,集中在活性基因的启动子-上游区域,在某些情况下在基因座范围内。使用超乙酰化H4抗体通过微球菌核酸酶消化,免疫沉淀源自K562人红血球白血病细胞的二核小体染色质。提取的DNA被制成基因组文库,并有望包含K562细胞中有活性的基因序列(有活性的“ aDNA”文库)。从库中随机选择克隆(180); 103个测试中的24个(23%)包含高度重复的序列,该序列是通过与总基因组DNA的杂交确定的,因此不做进一步分析。显示另外10个克隆(6%)不包含插入DNA。对其余的146个进行测序,并与核酸数据库进行比较,并在所有六个框架中与蛋白质数据库进行比较:可以将16个克隆分配给已知基因,其中大多数(12)是组织特异性的。如预期的那样,如果H4乙酰化集中在启动子区域,则这16个中除2个以外的所有部分均对应于编码序列的区段5'。 33个克隆(23%)与表达的序列标签数据库(dbEST)中的cDNA具有高度序列同一性。 Northern印迹和逆转录(RT)-PCR用于确定代表在K562细胞中表达的序列的克隆的比例:尽管34个测试克隆中只有1个显示出Northern杂交带,但RT-PCR显示,在40个测试克隆中至少有12个克隆(30%)存在于mRNA群体中。由于通过数据库序列比较将这40个克隆中的另外8个识别为基因片段,因此可以得出结论,这40个克隆的子集中约有一半来自基因。因此,aDNA文库的基因非常丰富,并且不像mRNA文库那样偏向最高度表达的序列。 aDNA文库也富含启动子,可能是此类序列的宝贵来源,尤其是缺少CpG岛或其他允许其特异性选择的特征的序列。

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