Asanuma H, Tamaru D, Yoshida T, Yamazawa A, Mitsui T, Okuni T, Kimoto M, Hirao I, Yokoyama S, Komiyama M
Research Center for Advanced Science and Technology, Univ. of Tokyo, Komaba, Meguro-ku, Tokyo 153-8904, Japan.
Nucleic Acids Res Suppl. 2001(1):55-6. doi: 10.1093/nass/1.1.55.
Transcription reaction by T7-RNA polymerase was photo-regulated on the basis of two strategies as depicted in Scheme 1. It was found that incorporation reaction of azobenzene-tethered uridine triphosphate proceeded only when azobenzene took trans-form (Scheme 1(A)). On the other hand, the transcription was more efficient when the azobenzene moiety, tethered to the non-template strand of the promoter DNA, was in its cis-form under UV irradiation (Scheme 1(B)). Thus, azobenzene-tethered DNAs are promising for the photo-regulation of gene-expression.
基于方案1中所描述的两种策略,T7 - RNA聚合酶的转录反应受到光调控。结果发现,只有当偶氮苯处于反式构象时,偶氮苯连接的三磷酸尿苷的掺入反应才会进行(方案1(A))。另一方面,当连接到启动子DNA非模板链上的偶氮苯部分在紫外线照射下处于顺式构象时,转录效率更高(方案1(B))。因此,偶氮苯连接的DNA有望用于基因表达的光调控。