Hu S Z, Wang T S, Korn D
J Biol Chem. 1984 Feb 25;259(4):2602-9.
The oligonucleotide primers synthesized by a highly purified KB fraction containing DNA primase and DNA polymerase-alpha activities display reproducible alterations of structure and composition in response to dNTPs. These observations are sufficiently explained by a novel model of primase catalysis that defines the primase as a complex enzyme with distinct catalytic properties that are regulated by mechanisms exquisitely sensitive to dNTP concentration. The enzyme performs the template-directed, de novo synthesis of 1 unit of oligoribonucleotide (canonical priming reaction) and then elongates that moiety to a limited extent by several cycles of addition of short tracts of homogeneous oligoribonucleotide or oligodeoxynucleotide. The oligomeric units have modal lengths of approximately 11- to 14- nucleotides that are postulated to reflect the inherent processivity of the catalytic mechanisms. Elongation is accomplished by two catalytic centers, or conformers of a single center, that are synchronously coupled, mutually exclusive, and extremely stringent for respective rNTP and dNTP substrates. Transitions between these two catalytic modes are regulated by dNTPs and demonstrable at dNTP:rNTP concentrations of less than or equal to 10(-4). In the absence of dNTPs, the primase produces a family of oligoribonucleotides, approximately 24- to 36- nucleotides long; at dNTP levels between 0.08 and 0.80 micron, the primase synthesizes mixed oligomers composed of strictly alternating tandem arrays of oligoribo- and oligodeoxynucleotide units; and at dNTP levels greater than or equal to 4.8 micron, the primase becomes stabilized in the deoxy mode after the initial oligoribo leads to oligodeoxy transition and products contain only a single 5' -terminal unit of oligoribonucleotide. The model predicts that the physiologically significant primer for DNA polymerase-alpha is a mixed 5' -oligoribo-3' -oligodeoxynucleotide and the signal which governs the switch from RNA leads to DNA synthesis is intrinsic in the primase mechanism and is generated by ambient dNTPs.
由含有DNA引发酶和DNA聚合酶α活性的高度纯化的KB组分合成的寡核苷酸引物,在dNTPs作用下,其结构和组成会发生可重复的变化。一种新的引发酶催化模型足以解释这些观察结果,该模型将引发酶定义为一种具有独特催化特性的复合酶,其催化特性受对dNTP浓度极为敏感的机制调控。该酶进行模板导向的、从头合成1个寡核糖核苷酸单位(典型的引发反应),然后通过添加短片段的同源寡核糖核苷酸或寡脱氧核苷酸的几个循环,将该部分延伸至有限程度。寡聚体单元的模式长度约为11至14个核苷酸,据推测这反映了催化机制固有的持续合成能力。延伸由两个催化中心或单个中心的构象异构体完成,它们同步耦合、相互排斥,且对各自的rNTP和dNTP底物极为严格。这两种催化模式之间的转变受dNTPs调控,并且在dNTP:rNTP浓度小于或等于10(-4)时可得到证明。在没有dNTPs的情况下,引发酶产生一系列长度约为24至36个核苷酸的寡核糖核苷酸;在dNTP水平为0.08至0.80微米之间时,引发酶合成由严格交替的寡核糖核苷酸和寡脱氧核苷酸单位串联阵列组成的混合寡聚物;在dNTP水平大于或等于4.8微米时,引发酶在初始寡核糖核苷酸向寡脱氧核苷酸转变后,在脱氧模式下变得稳定,产物仅包含单个5'-末端寡核糖核苷酸单位。该模型预测,DNA聚合酶α的生理上重要的引物是一种5'-寡核糖-3'-寡脱氧核苷酸混合物,并且控制从RNA引发向DNA合成转变的信号在引发酶机制中是固有的,由周围的dNTPs产生。