• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Chromosome structure and DNA sequence alterations associated with mutation of transformed genes.

作者信息

Robins D M, Axel R, Henderson A S

出版信息

J Mol Appl Genet. 1981;1(3):191-203.

PMID:6286823
Abstract

We have constructed a series of tk+ cell lines by DNA-mediated gene transfer to correlate chromosomal behavior and DNA sequence alterations associated with reversion to the tk- phenotype. Tk- revertants were selected from each of four well-characterized transformed cell lines containing the viral tk gene and multiple human growth hormone genes (HGH). Tk- colonies were analyzed for the presence of tk and HGH sequences by blot hybridization to restriction endonuclease cleaved DNA. Revertants were further characterized by detailed karyotype analysis and hybridization in situ. Blot hybridization of forty tk- revertants indicates that over half of the revertants delete all of the transforming DNA from the recipient chromosome. In fifteen additional revertants, significant deletion has occurred, although transforming DNA is retained. The analysis of chromosomes by Giemsa banding together with hybridization in situ reveals that the deletion of transforming DNA is never associated with loss of an entire chromosome. Reversion to the tk- phenotype, therefore, seems to involve discrete deletions of transforming DNA without apparent chromosome loss. In this restricted set of mutants, it thus seems crucial to maintain the diploid chromosomal complement.

摘要

相似文献

1
Chromosome structure and DNA sequence alterations associated with mutation of transformed genes.
J Mol Appl Genet. 1981;1(3):191-203.
2
Chromosome sorting and DNA sequence localization.染色体分选与DNA序列定位。
Cytometry. 1982 Nov;3(3):145-54. doi: 10.1002/cyto.990030302.
3
The structure and function of a eukaryotic promoter.真核生物启动子的结构与功能。
Princess Takamatsu Symp. 1982;12:73-85.
4
Deletion, rearrangement, and gene conversion; genetic consequences of chromosomal double-strand breaks in human cells.缺失、重排和基因转换;人类细胞中染色体双链断裂的遗传后果。
Environ Mol Mutagen. 2003;42(4):288-98. doi: 10.1002/em.10201.
5
Multicolor spectral karyotyping of the L5178Y Tk+/- -3.7.2C mouse lymphoma cell line.L5178Y Tk+/- -3.7.2C小鼠淋巴瘤细胞系的多色光谱核型分析
Environ Mol Mutagen. 2006 Mar;47(2):127-31. doi: 10.1002/em.20175.
6
[Characteristics of integration of monkey adenovirus SA7 DNA fragments with genomes of transformed and tumoral cells].[猴腺病毒SA7 DNA片段与转化细胞和肿瘤细胞基因组的整合特征]
Vopr Med Khim. 1983 May-Jun;29(3):14-22.
7
Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.通过比较基因组杂交(CGH)和CGH芯片分析的肝癌细胞系中的Y染色体丢失及其他基因组改变。
Cancer Genet Cytogenet. 2006 Apr 1;166(1):56-64. doi: 10.1016/j.cancergencyto.2005.08.022.
8
[Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].[神经母细胞瘤患者中一种先天性易位T(1;17)(p36;q12-21)的1号和17号染色体断点侧翼标记物的鉴定]
Verh K Acad Geneeskd Belg. 1995;57(5):389-422.
9
Molecular and cytogenetic characterization of site-specific repetitive DNA sequences in the Chinese soft-shelled turtle (Pelodiscus sinensis, Trionychidae).中华鳖(鳖科,中华鳖)位点特异性重复DNA序列的分子与细胞遗传学特征
Chromosome Res. 2005;13(1):33-46. doi: 10.1007/s10577-005-2351-0.
10
Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma cell line MG-63.联合光谱核型分析、多色带分析和微阵列比较基因组杂交分析为骨肉瘤细胞系MG-63中与基因扩增相关的复杂结构染色体重排提供了详细的特征描述。
Cancer Genet Cytogenet. 2004 Sep;153(2):158-64. doi: 10.1016/j.cancergencyto.2004.01.016.

引用本文的文献

1
Evolution of chromosomal regions containing transfected and amplified dihydrofolate reductase sequences.包含转染和扩增的二氢叶酸还原酶序列的染色体区域的演变。
Mol Cell Biol. 1983 Apr;3(4):699-711. doi: 10.1128/mcb.3.4.699-711.1983.
2
Changes in structure and methylation pattern in a cluster of thymidine kinase genes.一组胸苷激酶基因的结构和甲基化模式变化
Mol Cell Biol. 1984 Apr;4(4):611-7. doi: 10.1128/mcb.4.4.611-617.1984.
3
High-frequency mutation at the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells due to deletion of the gene.
中国仓鼠卵巢细胞中腺嘌呤磷酸核糖转移酶基因座因基因缺失而发生高频突变。
Proc Natl Acad Sci U S A. 1983 Feb;80(3):810-4. doi: 10.1073/pnas.80.3.810.
4
Homologous recombination between overlapping thymidine kinase gene fragments stably inserted into a mouse cell genome.稳定插入小鼠细胞基因组中的重叠胸苷激酶基因片段之间的同源重组。
Mol Cell Biol. 1984 May;4(5):852-61. doi: 10.1128/mcb.4.5.852-861.1984.
5
High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells.高频结构基因缺失作为中国仓鼠卵巢细胞中腺嘌呤磷酸核糖转移酶基因座功能半合子状态的基础。
Proc Natl Acad Sci U S A. 1983 Oct;80(19):5961-4. doi: 10.1073/pnas.80.19.5961.
6
Detection of deletion mutations in pSV2gpt-transformed cells.pSV2gpt转化细胞中缺失突变的检测。
Mol Cell Biol. 1984 Jul;4(7):1411-5. doi: 10.1128/mcb.4.7.1411-1415.1984.
7
Cre-stimulated recombination at loxP-containing DNA sequences placed into the mammalian genome.在置于哺乳动物基因组中的含loxP DNA序列处进行Cre刺激的重组。
Nucleic Acids Res. 1989 Jan 11;17(1):147-61. doi: 10.1093/nar/17.1.147.