首页> 外文期刊>The Journal of biological chemistry >The Cdc45·Mcm2–7·GINS Protein Complex in Trypanosomes Regulates DNA Replication and Interacts with Two Orc1-like Proteins in the Origin Recognition Complex
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The Cdc45·Mcm2–7·GINS Protein Complex in Trypanosomes Regulates DNA Replication and Interacts with Two Orc1-like Proteins in the Origin Recognition Complex

机译:TRYPANOSOMES中的谷蛋白蛋白复合物调节DNA复制,并在原始识别复合物中与两个奥氏蛋白相互作用

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Accurate DNA replication requires a complex interplay of many regulatory proteins at replication origins. The CMG (Cdc45·Mcm2–7·GINS) complex, which is composed of Cdc45, Mcm2–7, and the GINS (Go-Ichi-Ni-San) complex consisting of Sld5 and Psf1 to Psf3, is recruited by Cdc6 and Cdt1 onto origins bound by the heterohexameric origin recognition complex (ORC) and functions as a replicative helicase. Trypanosoma brucei, an early branched microbial eukaryote, appears to express an archaea-like ORC consisting of a single Orc1/Cdc6-like protein. However, unlike archaea, trypanosomes possess components of the eukaryote-like CMG complex, but whether they form an active helicase complex, associate with the ORC, and regulate DNA replication remains unknown. Here, we demonstrated that the CMG complex is formed in vivo in trypanosomes and that Mcm2–7 helicase activity is activated by the association with Cdc45 and the GINS complex in vitro. Mcm2–7 and GINS proteins are confined to the nucleus throughout the cell cycle, whereas Cdc45 is exported out of the nucleus after DNA replication, indicating that nuclear exclusion of Cdc45 constitutes one mechanism for preventing DNA re-replication in trypanosomes. With the exception of Mcm4, Mcm6, and Psf1, knockdown of individual CMG genes inhibits DNA replication and cell proliferation. Finally, we identified a novel Orc1-like protein, Orc1b, as an additional component of the ORC and showed that both Orc1b and Orc1/Cdc6 associate with Mcm2–7 via interactions with Mcm3. All together, we identified the Cdc45·Mcm2–7·GINS complex as the replicative helicase that interacts with two Orc1-like proteins in the unusual origin recognition complex in trypanosomes.
机译:准确的DNA复制需要在复制起源时许多调节蛋白的复杂相互作用。 CDC6和CDT1由CDC45,MCM2-7和由SLD5和PSF1组成的GC45,MCM2-7和GINS(GO-ICHI-NI-SAN)复合物组成的CMG(CDC45·MCM2-7·GINS)复合物通过异鸦透镜来源识别复合物(ORC)的起源和用作复制螺旋酶。胰蛋白酶体瘤Brucei是一种早期的分支微生物真核素,似乎表达了一种由单个ORC1 / CDC6样蛋白组成的古代ORC。然而,与古痤疮不同,锥虫具有真核状CMG复合物的组分,但它们是否形成活性螺旋酶复合物,与兽人相关联,并调节DNA复制仍然未知。在这里,我们证明CMG络合物在锥虫中形成体内,并且通过与CDC45和谷蛋白复合物在体外的胶质复合物激活MCM2-7螺旋酶活性。在整个细胞周期中,MCM2-7和谷蛋白蛋白被限制在核上,而DDC45在DNA复制后出口核,表明CDC45的核排除构成了防止DNA在锥虫中重新复制的一种机制。除MCM4,MCM6和PSF1外,单个CMG基因的敲低抑制DNA复制和细胞增殖。最后,我们鉴定了一种新的ORC1样蛋白,ORC1B,作为兽人的另外的组分,并显示ORC1B和ORC1 / CDC6通过与MCM3的相互作用与MCM2-7相关联。一切都在一起,我们确定了CDC45·MCM2-7·GINS复合物作为复制螺旋酶,其在锥虫中不寻常的起源识别复合物中与两个ORC1样蛋白相互作用。

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