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两种大鼠细胞系中特异性转化相关蛋白(TAPs)的合成与莫洛尼鼠肉瘤病毒(Mo-MSV)的v-mos基因产物的表达密切相关。

Synthesis of specific transformation-associated proteins (TAPs) in two rat cell lines is closely related to the expression of the v-mos gene product of Moloney murine sarcoma virus (Mo-MSV).

作者信息

Li W, Bowen J M, Chan J C

机构信息

Department of Tumor Biology, University of Texas, M.D. Anderson Hospital and Tumor Institute, Houston 77030.

出版信息

Intervirology. 1987;28(1):50-6. doi: 10.1159/000149996.

DOI:10.1159/000149996
PMID:2828268
Abstract

The 6M2 cell line was established by transformation of normal rat kidney cells with the ts110 mutant of Moloney murine sarcoma virus (Mo-MSV). P85gag-mos was found to be the only known viral-transforming protein in this cell system. Previously, we described the detection in 6M2 cells of rat-specific transformation-associated proteins (TAPs) using a monoclonal antibody (MC). In this study, we used MC to investigate further the expression of TAPs at different temperatures and the time course of turn-on and shut-off of TAPs upon temperature shifting. It was found that TAPs were expressed at 24, 28 and 33 degrees C, but not at 37 and 39 degrees C. In experiments of temperature shifting, TAPs reappeared in about 6 h in 6M2 cells after the temperature was shifted from 39 to 33 degrees C, following closely the reappearance of P85gag-mos. The data in this communication support the notion that TAPs might be activated by the v-mos gene product during the process of transformation.

摘要

6M2细胞系是通过用莫洛尼鼠肉瘤病毒(Mo-MSV)的ts110突变体转化正常大鼠肾细胞而建立的。P85gag-mos被发现是该细胞系统中唯一已知的病毒转化蛋白。此前,我们使用单克隆抗体(MC)描述了在6M2细胞中检测大鼠特异性转化相关蛋白(TAPs)的情况。在本研究中,我们使用MC进一步研究了TAPs在不同温度下的表达情况以及温度变化时TAPs开启和关闭的时间进程。结果发现,TAPs在24、28和33摄氏度时表达,但在37和39摄氏度时不表达。在温度变化实验中,当温度从39摄氏度转变为33摄氏度后,TAPs在6M2细胞中约6小时后重新出现,紧随P85gag-mos的重新出现。本通讯中的数据支持这样一种观点,即TAPs可能在转化过程中被v-mos基因产物激活。

相似文献

1
Synthesis of specific transformation-associated proteins (TAPs) in two rat cell lines is closely related to the expression of the v-mos gene product of Moloney murine sarcoma virus (Mo-MSV).两种大鼠细胞系中特异性转化相关蛋白(TAPs)的合成与莫洛尼鼠肉瘤病毒(Mo-MSV)的v-mos基因产物的表达密切相关。
Intervirology. 1987;28(1):50-6. doi: 10.1159/000149996.
2
Monoclonal antibody detection of transformation associated protein (TAP) in ts110 Moloney murine sarcoma virus transformed 6M2 cells that are different from the mos gene product.在ts110莫洛尼鼠肉瘤病毒转化的6M2细胞中,对不同于mos基因产物的转化相关蛋白(TAP)进行单克隆抗体检测。
Biochem Biophys Res Commun. 1986 Feb 13;134(3):1223-30. doi: 10.1016/0006-291x(86)90381-5.
3
Temperature-sensitive viral RNA expression in Moloney murine sarcoma virus ts110-infected cells.莫洛尼氏鼠肉瘤病毒ts110感染细胞中温度敏感型病毒RNA的表达
J Virol. 1985 Feb;53(2):616-23. doi: 10.1128/JVI.53.2.616-623.1985.
4
Temperature-sensitive splicing defect of ts110 Moloney murine sarcoma virus is virus encoded.ts110莫洛尼氏鼠肉瘤病毒的温度敏感剪接缺陷是由病毒编码的。
J Virol. 1986 Jan;57(1):301-9. doi: 10.1128/JVI.57.1.301-309.1986.
5
The gag-mos hybrid protein of ts110 Moloney murine sarcoma virus: variation of gene expression with temperature.ts110莫洛尼氏鼠肉瘤病毒的gag-mos杂合蛋白:基因表达随温度的变化
Virology. 1984 Dec;139(2):366-74. doi: 10.1016/0042-6822(84)90382-9.
6
Further characterization of the P85gag-mos -associated protein kinase activity.P85gag-mos相关蛋白激酶活性的进一步表征。
Virology. 1984 Oct 15;138(1):143-55. doi: 10.1016/0042-6822(84)90154-5.
7
A cAMP-independent serine/threonine kinase activity is associated with the mos sequences of ts110 Moloney murine sarcoma virus-encoded P85gag-mos.一种不依赖环磷酸腺苷(cAMP)的丝氨酸/苏氨酸激酶活性与ts110莫洛尼氏鼠肉瘤病毒编码的P85gag-mos的mos序列相关。
J Gen Virol. 1985 Oct;66 ( Pt 10):2135-46. doi: 10.1099/0022-1317-66-10-2135.
8
Molecular basis underlying phenotypic revertants of Moloney murine sarcoma virus MuSVts110.莫洛尼鼠肉瘤病毒MuSVts110表型回复突变体的分子基础。
J Virol. 1986 Jan;57(1):310-7. doi: 10.1128/JVI.57.1.310-317.1986.
9
P85gag-mos encoded by ts110 Moloney murine sarcoma virus: rapid at the restrictive temperature.由ts110莫洛尼氏鼠肉瘤病毒编码的P85gag-mos:在限制温度下迅速出现。
J Gen Virol. 1983 Oct;64 (Pt 10):2203-11. doi: 10.1099/0022-1317-64-10-2203.
10
Gag-mos Polyproteins encoded by variants of the Moloney strain of mouse sarcoma virus.莫洛尼氏小鼠肉瘤病毒变种编码的Gag-mos多聚蛋白。
Virology. 1983 Apr 15;126(1):336-47. doi: 10.1016/0042-6822(83)90483-x.