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Identification and functional analysis of PCNA1 and PCNA-like1 genes of Phaseolus coccineus

机译:菜豆PCNA1和PCNA-like1基因的鉴定和功能分析

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摘要

Proliferating cell nuclear antigen (PCNA) is an essential factor in DNA replication and in many other processes in eukaryotic cells. Genetic analysis of Phaseolus coccineus showed the presence of at least two PCNA-like genes in the runner bean genome. Two PCNA genes have previously been found in a few plant species including Arabidopsis, tobacco, and maize. In these species, genes were nearly identical. Two cDNAs of P. coccineus PCNA (PcPCNA1 and PcPCNA-like1) have been identified that differ distinctly from each other. Interestingly, both the genetic organization of PcPCNA1 and PcPCNA-like1 genes and their expression patterns were similar, but these were the only similarities between these genes and their products. The identity between PcPCNA1 and PcPCNA-like1 at the amino acid level was only 54%, with PcPCNA-like1 lacking motifs that are crucial for the activity typical of PCNA. Consequently, these two proteins showed different properties. PcPCNA1 behaved like a typical PCNA protein: it formed a homotrimer and stimulated the activity of human DNA polymerase delta. In addition, PcPCNA1 interacted with a p21 peptide and was recognized by an anti-human PCNA monoclonal antibody PC10. By contrast, PcPCNA-like1 was detected as a monomer and was unable to stimulate the DNA polymerase delta activity. PcPCNA-like1 also could not interact with p21 and was not recognized by the PC10 antibody. Our results suggest that PcPCNA-like1 either is unable to function alone and therefore might be a component of the heterotrimeric PCNA ring or may have other, yet unknown functions. Alternatively, the PcPCNA-like1 gene may represent a pseudogene.
机译:增殖细胞核抗原(PCNA)是真核细胞中DNA复制和许多其他过程中的重要因素。菜豆的菜豆的遗传分析表明,在菜豆基因组中至少存在两个PCNA样基因。先前已经在包括拟南芥,烟草和玉米在内的几种植物中发现了两个PCNA基因。在这些物种中,基因几乎相同。鉴定了两个球形的球形球菌PCNA cDNA(PcPCNA1和PcPCNA-like1)。有趣的是,PcPCNA1和PcPCNA-like1基因的遗传组织和它们的表达模式相似,但这是这些基因与其产物之间的唯一相似之处。 PcPCNA1和PcPCNA-like1在氨基酸水平上的同一性仅为54%,其中PcPCNA-like1缺少对PCNA典型活性至关重要的基序。因此,这两种蛋白质显示出不同的性质。 PcPCNA1的行为类似于典型的PCNA蛋白:它形成同源三聚体并刺激人类DNA聚合酶δ的活性。此外,PcPCNA1与p21肽相互作用,并被抗人PCNA单克隆抗体PC10识别。相比之下,PcPCNA-like1被检测为单体,不能刺​​激DNA聚合酶δ活性。 PcPCNA-like1也不能与p21相互作用,也不能被PC10抗体识别。我们的结果表明, Pc PCNA-like1不能单独发挥功能,因此可能是异三聚体PCNA环的组成部分,或者可能具有其他但未知的功能。或者, PcPCNA-like1 基因可能代表假基因。

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