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猴子富含起始位点(ors)片段之间的序列相似性。

Sequence similarities among monkey ori-enriched (ors) fragments.

作者信息

Rao B S, Zannis-Hadjopoulos M, Price G B, Reitman M, Martin R G

机构信息

Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892.

出版信息

Gene. 1990 Mar 15;87(2):233-42. doi: 10.1016/0378-1119(90)90307-d.

Abstract

Nucleotide sequences have been determined for eight ors (ori-enriched sequence) fragments isolated from monkey DNA by a method that was designed to enrich for origins of DNA replication [Kaufmann et al., Mol. Cell. Biol. 5 (1985) 721-727]. Evidence has been presented that some or possibly all of these sequences can serve, albeit inefficiently, as oris in vivo [Frappier and Zannis-Hadjopoulos, Proc. Natl. Acad. Sci. USA 84 (1987) 6668-6672]. Two of the fragments were found to contain the long terminal repeat-like elements of the 'O-family' of moderately repetitive sequences that are present in human DNA as a transposon-like element [Paulson et al., Nature 315 (1985) 359-361]. Extensive pair-wise comparisons of the sequences failed to detect any statistically significant common sequences, except for long asymmetrically distributed A + T-rich stretches. Nonetheless, when the ors fragments were examined for the presence of published consensus sequences, seven of eight were found to contain the control sequence described by Dierks et al. [Cell 32 (1983) 695-706], and the same seven of eight were found to contain both the scaffold attachment region T consensus [Gasser and Laemmli, Cell 46 (1986) 521-530] and the minimal Saccharomyces cerevisiae autonomously replicating sequence consensus [e.g., Palzkill and Newlon, Cell 53 (1988) 441-450].

摘要

通过一种旨在富集DNA复制起点的方法,从猴DNA中分离出了8个富含ori(ori富集序列)的片段,并测定了其核苷酸序列[考夫曼等人,《分子细胞生物学》5(1985)721 - 727]。有证据表明,这些序列中的一些或可能全部,尽管效率不高,但在体内可作为复制起点[弗拉皮尔和赞尼斯 - 哈乔普洛斯,《美国国家科学院院刊》84(1987)6668 - 6672]。发现其中两个片段含有中度重复序列“O家族”的长末端重复样元件,这些元件在人类DNA中作为转座子样元件存在[保尔森等人,《自然》315(1985)359 - 361]。除了长的不对称分布的富含A + T的片段外,对这些序列进行广泛的两两比较未能检测到任何具有统计学意义的共同序列。尽管如此,当检查ori片段是否存在已发表的共有序列时,发现8个片段中的7个含有迪克斯等人[《细胞》32(1983)695 - 706]描述的控制序列,并且8个片段中的相同7个被发现同时含有支架附着区域T共有序列[加塞尔和莱姆利,《细胞》46(1986)521 - 530]和酿酒酵母最小自主复制序列共有序列[例如,帕尔兹基尔和纽隆,《细胞》53(1988)441 - 450]。

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