Nguyen T P, Kmiec E B
Jefferson Cancer Institute, Thomas Jefferson School of Medicine, Philadelphia, Pennsylvania 19107.
Mol Cell Biochem. 1993 Mar 10;120(1):33-41. doi: 10.1007/BF00925982.
The first exon of the human c-myc gene can be transcribed by either RNA polymerase II or RNA polymerase III. The molecular factors contributing to polymerase selection are not yet completely defined. We have examined the role of chromatin structure in regulating transcription by RNA polymerase III. Using as competitor a pol III gene in both a cis and trans arrangement, we demonstrate that c-myc gene expression is facilitated from templates containing a minimal number of fully assembled nucleosomes. The removal of excess histones by DNA titration leads to an elevated level of c-myc expression. These results suggest that either the c-myc expression is inhibited when the template is fully packaged into chromatin or that the affinity of RNA polymerase for the regulatory elements of this exon is such that a template, devoid of histones, is required for transcriptional initiation.
人类c-myc基因的第一个外显子可由RNA聚合酶II或RNA聚合酶III转录。导致聚合酶选择的分子因素尚未完全明确。我们研究了染色质结构在RNA聚合酶III调控转录中的作用。使用顺式和反式排列的pol III基因作为竞争者,我们证明,从含有最少量完全组装核小体的模板中,c-myc基因表达更容易。通过DNA滴定去除过量组蛋白会导致c-myc表达水平升高。这些结果表明,要么当模板完全包装成染色质时c-myc表达受到抑制,要么RNA聚合酶对该外显子调控元件的亲和力使得转录起始需要一个不含组蛋白的模板。