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Cloning and characterization of a cDNA encoding topoisomerase II in pea and analysis of its expression in relation to cell proliferation

机译:豌豆中编码拓扑异构酶Ⅱ的cDNA的克隆,鉴定及其与细胞增殖相关的表达分析

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We have isolated and sequenced four overlapping cDNA clones to identify the full-length cDNA for topoisomerase II (PsTopII) from pea. Using degenerate primers, based on the conserved amino acid sequences of other eukaryotic type II topoisomerases, a 680 bp fragment was PCR-amplified with pea cDNA as template. This fragment was used as a probe to screen an oligo-dT-primed pea cDNA library. A partial cDNA clone was isolated that was truncated at the 3' end. RACE-PCR was employed to isolate the remaining portion of the gene. The total size of PsTopII is 4639 bp with an open reading frame of 4392 bp. The deduced amino acid sequence shows a strong homology to other eukaryotic topoisomerase II (topo II) at the N-terminus end. The topo II transcript was abundant in proliferative tissues. We also show that the level of topo II transcripts could be stimulated by exogenous application of growth factors that induced proliferation in vitro cultures. Light irradiation to etiolated tissue strongly stimulated the expression of topo II. These results suggest that topo II gene expression is up-regulated in response to light and hormones and correlates with cell proliferation. Besides, we have also isolated and analysed the 5'-flanking region of the pea TopII gene. This is first report on the isolation of a putative promoter for topoisomerase II from plants.
机译:我们已经分离并测序了四个重叠的cDNA克隆,以鉴定来自豌豆的拓扑异构酶II(PsTopII)的全长cDNA。使用简并引物,基于其他II型真核拓扑异构酶的保守氨基酸序列,以豌豆cDNA为模板PCR扩增680 bp的片段。该片段用作探针,以寡聚dT-primed豌豆cDNA文库。分离了部分cDNA克隆,其在3'端被截短。使用RACE-PCR分离基因的其余部分。 PsTopII的总大小为4639 bp,开放阅读框为4392 bp。推导的氨基酸序列在N末端与其他真核拓扑异构酶II(topo II)具有很强的同源性。 topo II转录本在增生组织中含量很高。我们还显示,外源应用生长因子可诱导体外培养的增殖,从而刺激topo II转录本的水平。光照射到黄化的组织中强烈刺激了topo II的表达。这些结果表明,topo II基因表达上调响应光和激素,并与细胞增殖相关。此外,我们还分离并分析了豌豆TopII基因的5'侧翼区域。这是关于从植物中分离出拓扑异构酶II的推定启动子的首次报道。

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