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人类鸟氨酸脱羧酶序列定位于染色体区域2pter----p23和7cen----qter,但不与NMYC癌基因共同扩增。

Human ornithine decarboxylase sequences map to chromosome regions 2pter----p23 and 7cen----qter but are not coamplified with the NMYC oncogene.

作者信息

Winqvist R, Mäkelä T P, Seppänen P, Jänne O A, Alhonen-Hongisto L, Jänne J, Grzeschik K H, Alitalo K

出版信息

Cytogenet Cell Genet. 1986;42(3):133-40. doi: 10.1159/000132266.

Abstract

Using a mouse cDNA probe for ornithine decarboxylase (ODC), we have identified and isolated an ODC cDNA clone from a lambda gt11 recombinant library prepared from human liver cell mRNA. The 2.0-kb insert of this clone hybridizes with several mouse genomic ODC DNA restriction fragments under conditions of low stringency, but reacts with only few human DNA fragments and a polyA+ RNA species of 2.2 kb under both nonstringent and stringent hybridization conditions. This suggests that, unlike the mouse genome, there are only few ODC genes in the human genome. The human ODC DNA fragments segregate with chromosome regions 2pter----p23 and 7cen----qter in mouse X human somatic cell hybrid clones containing normal, translocated, and deleted human chromosomes. Sequences of the short arm of chromosome 2 containing the NMYC oncogene at 2p23----p24 are often involved in DNA amplification in neuroblastomas and small-cell lung cancers. However, in at least three cases--one neuroblastoma cell line, one neuroblastoma tumor, and one lung carcinoma--the ODC sequences are not coamplified with the NMYC oncogene.

摘要

我们使用鸟氨酸脱羧酶(ODC)的小鼠cDNA探针,从一个由人肝细胞mRNA构建的λgt11重组文库中鉴定并分离出一个ODC cDNA克隆。在低严谨度条件下,该克隆的2.0kb插入片段能与几个小鼠基因组ODC DNA限制性片段杂交,但在非严谨和严谨杂交条件下,仅与少数人类DNA片段以及一个2.2kb的polyA + RNA种类发生反应。这表明,与小鼠基因组不同,人类基因组中只有少数ODC基因。在含有正常、易位和缺失人类染色体的小鼠×人类体细胞杂种克隆中,人类ODC DNA片段与染色体区域2pter----p23和7cen----qter分离。位于2p23----p24含有NMYC癌基因的2号染色体短臂序列,在神经母细胞瘤和小细胞肺癌中常参与DNA扩增。然而,在至少三例中——一个神经母细胞瘤细胞系、一个神经母细胞瘤肿瘤和一个肺癌——ODC序列并未与NMYC癌基因共同扩增。

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