Hernandez Alfredo J, Lee Seung-Joo, Richardson Charles C
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115
Proc Natl Acad Sci U S A. 2016 May 24;113(21):5916-21. doi: 10.1073/pnas.1604894113. Epub 2016 May 9.
DNA replication occurs semidiscontinuously due to the antiparallel DNA strands and polarity of enzymatic DNA synthesis. Although the leading strand is synthesized continuously, the lagging strand is synthesized in small segments designated Okazaki fragments. Lagging-strand synthesis is a complex event requiring repeated cycles of RNA primer synthesis, transfer to the lagging-strand polymerase, and extension effected by cooperation between DNA primase and the lagging-strand polymerase. We examined events controlling Okazaki fragment initiation using the bacteriophage T7 replication system. Primer utilization by T7 DNA polymerase is slower than primer formation. Slow primer release from DNA primase allows the polymerase to engage the complex and is followed by a slow primer handoff step. The T7 single-stranded DNA binding protein increases primer formation and extension efficiency but promotes limited rounds of primer extension. We present a model describing Okazaki fragment initiation, the regulation of fragment length, and their implications for coordinated leading- and lagging-strand DNA synthesis.
由于DNA链的反平行性和酶促DNA合成的极性,DNA复制以半不连续方式进行。尽管前导链是连续合成的,但滞后链是由称为冈崎片段的小片段合成的。滞后链合成是一个复杂的过程,需要RNA引物合成、转移到滞后链聚合酶以及DNA引发酶和滞后链聚合酶之间协同作用进行延伸的重复循环。我们使用噬菌体T7复制系统研究了控制冈崎片段起始的事件。T7 DNA聚合酶对引物的利用比引物形成要慢。从DNA引发酶缓慢释放引物使得聚合酶能够结合该复合物,随后是一个缓慢的引物交接步骤。T7单链DNA结合蛋白提高了引物形成和延伸效率,但促进了有限轮次的引物延伸。我们提出了一个描述冈崎片段起始、片段长度调节及其对前导链和滞后链DNA合成协调影响的模型。