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线粒体 DNA 引发酶对于布鲁氏锥虫细胞生长和动基体 DNA 复制是必需的。

A mitochondrial DNA primase is essential for cell growth and kinetoplast DNA replication in Trypanosoma brucei.

机构信息

Molecular Biology Institute and Department of Microbiology, Immunology and Molecular Genetics, UCLA, Los Angeles, California 90095-1570, USA.

出版信息

Mol Cell Biol. 2010 Mar;30(6):1319-28. doi: 10.1128/MCB.01231-09. Epub 2010 Jan 11.

Abstract

Kinetoplast DNA in African trypanosomes contains a novel form of mitochondrial DNA consisting of thousands of minicircles and dozens of maxicircles topologically interlocked to form a two-dimensional sheet. The replication of this unusual form of mitochondrial DNA has been studied for more than 30 years, and although a large number of kinetoplast replication genes and proteins have been identified, in vitro replication of these DNAs has not been possible since a kinetoplast DNA primase has not been available. We describe here a Trypanosoma brucei DNA primase gene, PRI1, that encodes a 70-kDa protein that localizes to the kinetoplast and is essential for both cell growth and kinetoplast DNA replication. The expression of PRI1 mRNA is cyclic and reaches maximum levels at a time corresponding to duplication of the kinetoplast DNA. A 3'-hydroxyl-terminated oligoriboadenylate is synthesized on a poly(dT) template by a recombinant form of the PRI1 protein and is subsequently elongated by DNA polymerase and added dATP. Poly(dA) synthesis is dependent on both PRI1 protein and ATP and is inhibited by RNase H treatment of the product of PRI1 synthesis.

摘要

动基体 DNA 含有一种新型的线粒体 DNA,由数千个小型环和数十个大型环拓扑相互连接形成二维片层。这种不寻常形式的线粒体 DNA 的复制已经研究了 30 多年,尽管已经鉴定出大量的动基体复制基因和蛋白质,但由于没有动基体 DNA 引物酶,这些 DNA 的体外复制仍然不可能。我们在这里描述了一种布鲁氏锥虫 DNA 引物酶基因 PRI1,它编码一种 70kDa 的蛋白质,定位于动基体,对于细胞生长和动基体 DNA 复制都是必需的。PRI1 mRNA 的表达是周期性的,在与动基体 DNA 复制相对应的时间达到最大值。一种 3'-羟基末端寡聚腺苷酸通过 PRI1 蛋白的重组形式在聚(dT)模板上合成,并随后由 DNA 聚合酶和添加的 dATP 延伸。多聚(dA)的合成依赖于 PRI1 蛋白和 ATP,并且产物的 RNase H 处理会抑制 PRI1 合成。

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