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拟南芥中核DNA拓扑异构酶II的丰度与细胞增殖相关。

Abundance of nuclear DNA topoisomerase II is correlated with proliferation in Arabidopsis thaliana.

作者信息

Xie S, Lam E

机构信息

AgBiotech Center, Piscataway, NJ.

出版信息

Nucleic Acids Res. 1994 Dec 25;22(25):5729-36. doi: 10.1093/nar/22.25.5729.

Abstract

Topoisomerase II (TOPII) is an important enzyme involved in DNA replication and chromosome condensation. The level of TOPII expression has been correlated with the proliferative state of eukaryotic cells. Here we report the cloning and characterization of a cDNA clone AtTopII encoding the first reported TOPII from higher plants. AtTopII is 4603 base pairs (bp) in length and encodes an open reading frame of 1473 amino acid residues. One interesting feature of AtTopII is the presence of a 110 bp direct repeat in the last one-third of the cDNA. Analysis of the genomic sequence within this region by PCR revealed that this duplication includes a small intron of 89 bp. Conservation of sequences within this repeated intron suggests that this in-frame duplication may be a relatively recent event. The deduced amino acid sequence of AtTopII shows strong homologies to TOPII sequences reported from other eukaryotes, particularly in the regions that are highly conserved among different species. Southern blot analysis with Arabidopsis DNA indicates that AtTopII is a single-copy gene while Northern blots detected a 5.0 kb transcript, the level of which is substantially higher in young seedlings than in mature plants. Using a polyclonal antiserum raised against the C-terminal one-third of AtTOPII, we found that the protein is localized in the nucleus and its level is correlated with the proliferative state of the particular tissue.

摘要

拓扑异构酶II(TOPII)是一种参与DNA复制和染色体浓缩的重要酶。TOPII的表达水平与真核细胞的增殖状态相关。在此,我们报道了一个编码高等植物中首个报道的TOPII的cDNA克隆AtTopII的克隆及特性分析。AtTopII长度为4603个碱基对(bp),编码一个由1473个氨基酸残基组成的开放阅读框。AtTopII的一个有趣特征是在cDNA的最后三分之一处存在一个110 bp的直接重复序列。通过PCR对该区域内的基因组序列进行分析发现,这种重复包括一个89 bp的小内含子。该重复内含子内序列的保守性表明,这种框内重复可能是一个相对较新的事件。AtTopII推导的氨基酸序列与其他真核生物报道的TOPII序列具有很强的同源性,特别是在不同物种间高度保守的区域。用拟南芥DNA进行的Southern印迹分析表明AtTopII是一个单拷贝基因,而Northern印迹检测到一个5.0 kb的转录本,其水平在幼苗中明显高于成熟植株。使用针对AtTOPII C端三分之一区域制备的多克隆抗血清,我们发现该蛋白定位于细胞核,其水平与特定组织的增殖状态相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/903d/310140/e33c1eb6b99e/nar00049-0216-a.jpg

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