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在广古菌DNA复制过程中与增殖细胞核抗原(PCNA)结合,DNA聚合酶D需要两个增殖细胞核抗原相互作用基序(PIP基序),而DNA聚合酶B需要一个PIP基序。

Binding to PCNA in Euryarchaeal DNA Replication requires two PIP motifs for DNA polymerase D and one PIP motif for DNA polymerase B.

作者信息

Castrec Benoît, Rouillon Christophe, Henneke Ghislaine, Flament Didier, Querellou Joël, Raffin Jean-Paul

机构信息

Université de Bretagne Occidentale, UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes, BP 70, F-29280 Plouzané, France.

出版信息

J Mol Biol. 2009 Nov 27;394(2):209-18. doi: 10.1016/j.jmb.2009.09.044. Epub 2009 Sep 23.

DOI:10.1016/j.jmb.2009.09.044
PMID:19781553
Abstract

Replicative DNA polymerases possess a canonical C-terminal proliferating cell nuclear antigen (PCNA)-binding motif termed the PCNA-interacting protein (PIP) box. We investigated the role of the PIP box on the functional interactions of the two DNA polymerases, PabPol B (family B) and PabPol D (family D), from the hyperthermophilic euryarchaeon Pyrococcus abyssi, with its cognate PCNA. The PIP box was essential for interactions of PabPol B with PCNA, as shown by surface plasmon resonance and primer extension studies. In contrast, binding of PabPol D to PCNA was affected only partially by removing the PIP motif. We identified a second palindromic PIP box motif at the N-terminus of the large subunit of PabPol D that was required for the interactions of PabPol D with PCNA. Thus, two PIP motifs were needed for PabPol D for binding to PabPCNA. Moreover, the C-terminus of PabPCNA was essential for stimulation of PabPol D activity but not for stimulation of PabPol B activity. Neither DNA polymerase interacted with the PabPCNA interdomain connecting loop. Our data suggest that distinct processes are involved in PabPol D and PabPol B binding to PCNA, raising the possibility that Archaea require two mechanisms for recruiting replicative DNA polymerases at the replication fork.

摘要

复制性DNA聚合酶具有一个典型的C端增殖细胞核抗原(PCNA)结合基序,称为PCNA相互作用蛋白(PIP)框。我们研究了PIP框在嗜热古菌深渊热球菌的两种DNA聚合酶PabPol B(B家族)和PabPol D(D家族)与其同源PCNA的功能相互作用中的作用。表面等离子体共振和引物延伸研究表明,PIP框对于PabPol B与PCNA的相互作用至关重要。相比之下,去除PIP基序仅部分影响PabPol D与PCNA的结合。我们在PabPol D大亚基的N端鉴定出第二个回文PIP框基序,它是PabPol D与PCNA相互作用所必需的。因此,PabPol D需要两个PIP基序来结合PabPCNA。此外,PabPCNA的C端对于刺激PabPol D的活性至关重要,但对刺激PabPol B的活性并非必需。两种DNA聚合酶均未与PabPCNA结构域间连接环相互作用。我们的数据表明,PabPol D和PabPol B与PCNA的结合涉及不同的过程,这增加了古菌在复制叉处募集复制性DNA聚合酶需要两种机制的可能性。

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