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分子克隆的c-mos(大鼠)具有生物活性。

Molecularly cloned c-mos(rat) is biologically active.

作者信息

van der Hoorn F A, Hulsebos E, Berns A J, Bloemers H P

出版信息

EMBO J. 1982;1(11):1313-7. doi: 10.1002/j.1460-2075.1982.tb01316.x.

Abstract

A unique rat cellular gene, c-mos(rat), homologous to the transforming sequences, v-mos, of Moloney murine sarcoma virus (M-MSV) was detected by hybridization to a v-mos specific probe. The c-mos(rat) gene was cloned together with its flanking sequences in an 11-kbp EcoRI DNA fragment inserted in vector Charon 4A. Two probes were used to investigate the position and orientation of c-mos(rat) in the clone examined ( D3e ), namely pMSV -31 which contains the sequences specific for the transforming sequences of M-MSV and pCS-1 which harbors 0.5 kbp of 5'-terminal sequences of c-mos(mouse) as well as 0.7 kbp of its flanking sequences. After ligation of a restriction fragment of clone D3e containing c-mos(rat) to a fragment containing the long terminal repeat of M-MSV and transfection of the DNA onto rat cells, we detected foci of transformed cells, thus showing that c-mos(rat) is biologically active. Using DNA framents derived from clone D3e , we studied the conservation of c-mos and of its flanking sequences in several species. c-mos(rat) as well as some of its flanking sequences appeared to be highly conserved in the species studied.

摘要

通过与v-mos特异性探针杂交,检测到一种独特的大鼠细胞基因c-mos(大鼠),它与莫洛尼氏鼠肉瘤病毒(M-MSV)的转化序列v-mos同源。c-mos(大鼠)基因与其侧翼序列一起被克隆到插入载体Charon 4A的一个11kbp的EcoRI DNA片段中。使用两个探针来研究c-mos(大鼠)在所检测克隆(D3e)中的位置和方向,即包含M-MSV转化序列特异性序列的pMSV -31和含有c-mos(小鼠) 5'末端序列0.5kbp及其侧翼序列0.7kbp的pCS-1。将含有c-mos(大鼠)的克隆D3e的一个限制性片段与含有M-MSV长末端重复序列的片段连接,并将该DNA转染到大鼠细胞后,我们检测到了转化细胞集落,从而表明c-mos(大鼠)具有生物学活性。利用来自克隆D3e的DNA片段,我们研究了c-mos及其侧翼序列在几个物种中的保守性。c-mos(大鼠)及其一些侧翼序列在所研究的物种中似乎高度保守。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a525/553210/66a36b9b5ab4/emboj00303-0026-a.jpg

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