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大鼠鸟氨酸脱羧酶cDNA的克隆与核苷酸序列

Cloning and nucleotide sequence of rat ornithine decarboxylase cDNA.

作者信息

van Kranen H J, van de Zande L, van Kreijl C F, Bisschop A, Wieringa B

机构信息

National Institute of Public Health and Environmental Hygiene, Bilthoven, The Netherlands.

出版信息

Gene. 1987;60(2-3):145-55. doi: 10.1016/0378-1119(87)90222-8.

Abstract

The enzyme ornithine decarboxylase (ODC; EC 4.1.1.17) catalyses the first and rate-limiting step in polyamine biosynthesis. Its activity is markedly increased in rapidly growing or regenerating tissue and is subject to regulation by a variety of trophic and mitogenic stimuli. ODC is therefore believed to play an essential role in the onset of cellular proliferation. In a molecular-biological approach to investigate ODC regulation upon induction by tumor promoters in rat liver we isolated an almost full-length rat ODC cDNA clone of 2.4 kb (designated pODC.E10) from a cDNA library of testosterone-induced rat kidney poly(A)+ RNA. Characterization by restriction-endonuclease mapping and sequence analysis showed strong homology to mouse ODC cDNA sequences previously published [Gupta and Coffino, J. Biol. Chem. 260 (1985) 2941-2944; Kahana and Nathans, Proc. Natl. Acad. Sci. USA 82 (1985) 1673-1677; Hickok et al., Proc. Natl. Acad. Sci. USA 83 (1986) 594-598]. This homology is most pronounced in the 461-aa-spanning coding region, amounting to 94% and 97% at the DNA and protein levels, respectively. In the 423-nt 5' leader the rat-mouse homology (approx. 75%) is most pronounced in a region of about 175 nt directly upstream from the translational start site. The leader sequence also contains a perfect inverted repeat of 54 nt and ten additional upstream ATG triplets, which are all followed by nonsense codons before the initiating ATG. In the 633-nt 3' trailer region of pODC.E10 an additional polyadenylation signal is observed more than 300 nt upstream from the 3' end. Rat-mouse homology is about 80% up to this first polyadenylation signal and is considerably less thereafter. The presence of two alternate polyadenylation sites most likely accounts for the 3' size heterogeneity observed in the two ODC mRNAs of 2.1 and 2.6 kb, respectively. In rat liver both mRNAs are coordinately induced by different tumor promoters. Finally, Southern blot analysis of normal rat liver and rat hepatoma DNA revealed that rat ODC, as in other rodents, belongs to a multigene family.

摘要

鸟氨酸脱羧酶(ODC;EC 4.1.1.17)催化多胺生物合成的第一步且是限速步骤。其活性在快速生长或再生的组织中显著增加,并受到多种营养和促有丝分裂刺激的调节。因此,ODC被认为在细胞增殖的起始过程中起重要作用。在一项分子生物学研究中,为了探究大鼠肝脏中肿瘤启动子诱导后ODC的调控机制,我们从睾酮诱导的大鼠肾脏多聚腺苷酸加尾RNA的cDNA文库中分离出一个2.4 kb的几乎全长的大鼠ODC cDNA克隆(命名为pODC.E10)。通过限制性内切酶图谱分析和序列分析进行的特征鉴定表明,它与先前发表的小鼠ODC cDNA序列具有高度同源性[古普塔和科菲诺,《生物化学杂志》260(1985)2941 - 2944;卡哈纳和内森斯,《美国国家科学院院刊》82(1985)1673 - 1677;希科克等人,《美国国家科学院院刊》83(1986)594 - 598]。这种同源性在跨越461个氨基酸的编码区域最为明显,在DNA和蛋白质水平上分别达到94%和97%。在423个核苷酸的5'前导序列中,大鼠与小鼠的同源性(约75%)在翻译起始位点上游约175个核苷酸的区域最为明显。前导序列还包含一个54个核苷酸的完美反向重复序列和另外10个上游ATG三联体,在起始ATG之前它们后面都跟着无义密码子。在pODC.E10的633个核苷酸的3'拖尾区域,在3'末端上游300多个核苷酸处观察到一个额外的聚腺苷酸化信号。直到这个第一个聚腺苷酸化信号,大鼠与小鼠的同源性约为80%,此后则明显降低。两个交替聚腺苷酸化位点的存在很可能解释了分别在2.1 kb和2.6 kb的两种ODC mRNA中观察到的3'大小异质性。在大鼠肝脏中,这两种mRNA都受到不同肿瘤启动子的协同诱导。最后,对正常大鼠肝脏和大鼠肝癌DNA的Southern印迹分析表明,大鼠ODC与其他啮齿动物一样,属于一个多基因家族。

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