Nam K, Hudson R H, Chapman K B, Ganeshan K, Damha M J, Boeke J D
Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2185.
J Biol Chem. 1994 Aug 12;269(32):20613-21.
Yeast RNA lariat debranching enzyme has been purified to near homogeneity using a bacterial overproducer of the enzyme. The enzyme is capable of digesting a variety of branched nucleic acid substrates, including group II intron lariats, multicopy single-stranded DNAs (msDNAs), and a variety of synthetic branched RNAs. A trinucleotide release assay using radiolabeled msDNA substrates was developed and used to determine the basic biochemical parameters for the enzyme. The debranching enzyme shows a strong preference for purines at the 2'-position in both msDNA and synthetic branched RNA substrates, in accord with the structure of its native substrate, which always has a 2'-G residue. The use of small synthetic branched RNA substrates will allow systematic mechanistic and structural studies of this unique enzyme.
利用该酶的细菌过量表达菌株,已将酵母RNA套索脱支酶纯化至接近均一的状态。该酶能够消化多种分支核酸底物,包括II类内含子套索、多拷贝单链DNA(msDNA)以及多种合成分支RNA。开发了一种使用放射性标记的msDNA底物的三核苷酸释放测定法,并用于确定该酶的基本生化参数。脱支酶在msDNA和合成分支RNA底物的2'-位置对嘌呤表现出强烈偏好,这与其天然底物的结构一致,其天然底物总是具有2'-G残基。使用小的合成分支RNA底物将有助于对这种独特的酶进行系统的机制和结构研究。