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1
Evidence that the AKR murine-leukemia-virus genome is complete in DNA of the high-virus AKR mouse and incomplete in the DNA of the "virus-negative" NIH mouse.有证据表明,AKR鼠白血病病毒基因组在高病毒血症AKR小鼠的DNA中是完整的,而在“病毒阴性”NIH小鼠的DNA中是不完整的。
Proc Natl Acad Sci U S A. 1974 Jan;71(1):167-71. doi: 10.1073/pnas.71.1.167.
2
Qualitative and quantitative studies of AKR-type murine leukemia virus sequences in mouse DNA.小鼠DNA中AKR型鼠白血病病毒序列的定性和定量研究。
Cold Spring Harb Symp Quant Biol. 1975;39 Pt 2:1085-101. doi: 10.1101/sqb.1974.039.01.124.
3
AKR murine leukemia virus genome: frequency of sequences in DNA of high-, low-, and non-virus-yielding mouse strains.AKR鼠白血病病毒基因组:高产、低产和不产病毒小鼠品系DNA中序列的频率
Proc Natl Acad Sci U S A. 1974 Sep;71(9):3555-9. doi: 10.1073/pnas.71.9.3555.
4
Quantitative studies of integration of murine leukemia virus after exogenous infection.外源感染后小鼠白血病病毒整合的定量研究。
Proc Natl Acad Sci U S A. 1976 Nov;73(11):4095-9. doi: 10.1073/pnas.73.11.4095.
5
Differences in murine leukaemia virus-specific DNA sequences in normal and malignant cells.正常细胞与恶性细胞中鼠白血病病毒特异性DNA序列的差异。
Nature. 1973;246(5434):485-7. doi: 10.1038/246485a0.
6
Definitive evidence that the murine C-type virus inducing locus Akv-1 is viral genetic material.诱导小鼠C型病毒的位点Akv-1是病毒遗传物质的确切证据。
Proc Natl Acad Sci U S A. 1975 Mar;72(3):906-10. doi: 10.1073/pnas.72.3.906.
7
Detection of AKR MuLV-specific RNA in AKR mouse cells by in situ hybridization.通过原位杂交检测AKR小鼠细胞中AKR MuLV特异性RNA。
Nucleic Acids Res. 1979 Jun 25;6(8):2849-61. doi: 10.1093/nar/6.8.2849.
8
Correlation of the induction of transcription of the AKR mouse genome 5-lododeoxyuridine with the activation of an endogenous murine leukemia virus.AKR小鼠基因组5-碘脱氧尿苷转录诱导与内源性鼠白血病病毒激活的相关性。
Cancer Res. 1979 May;39(5):1539-46.
9
Increase of AKR-specific sequences in tumor tissues of leukemic AKR mice.白血病AKR小鼠肿瘤组织中AKR特异性序列的增加。
Proc Natl Acad Sci U S A. 1976 Jul;73(7):2448-52. doi: 10.1073/pnas.73.7.2448.
10
Characterization of murine leukaemia virus-specific DNA present in normal mouse cells.正常小鼠细胞中存在的鼠白血病病毒特异性DNA的特性分析。
Nat New Biol. 1973 Jul 18;244(133):76-9. doi: 10.1038/newbio244076a0.

引用本文的文献

1
A quantitative trait locus responsible for inducing B-cell lymphoblastic lymphoma is a hotspot for microsatellite instability.一个导致 B 细胞淋巴母细胞淋巴瘤的数量性状位点是微卫星不稳定的热点。
Cancer Sci. 2010 Mar;101(3):800-5. doi: 10.1111/j.1349-7006.2009.01437.x.
2
Lymphomas and high-level expression of murine leukemia viruses in CFW mice.CFW小鼠中的淋巴瘤与鼠白血病病毒的高水平表达
J Virol. 2000 Aug;74(15):6832-7. doi: 10.1128/jvi.74.15.6832-6837.2000.
3
Structure of retroviral RNAs produced by cell lines derived from spontaneous lymphomas of AKR mice.源自AKR小鼠自发性淋巴瘤的细胞系所产生的逆转录病毒RNA的结构
J Virol. 1982 Jan;41(1):18-29. doi: 10.1128/JVI.41.1.18-29.1982.
4
Expression of endogenous retroviral glycoprotein 70 by antigen-activated cytotoxic and suppressor T lymphocytes of nice.内源性逆转录病毒糖蛋白70在正常小鼠抗原激活的细胞毒性和抑制性T淋巴细胞中的表达
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1250-3. doi: 10.1073/pnas.79.4.1250.
5
A novel sequence segment and other nucleotide structural features in the long terminal repeat of a BALB/c mouse genomic leukemia virus-related DNA clone.BALB/c小鼠基因组白血病病毒相关DNA克隆的长末端重复序列中的一个新序列片段及其他核苷酸结构特征。
Nucleic Acids Res. 1983 Aug 25;11(16):5603-20. doi: 10.1093/nar/11.16.5603.
6
Kinetics of expression of infectious ecotropic, xenotropic, and mink cell focus-forming murine leukemia virus after 5-iododeoxyuridine induction of cells from high- and low-leukemia mouse strains.用5-碘脱氧尿苷诱导高白血病和低白血病小鼠品系的细胞后,感染性亲嗜性、异嗜性和貂细胞集落形成性鼠白血病病毒的表达动力学
J Virol. 1983 Feb;45(2):755-65. doi: 10.1128/JVI.45.2.755-765.1983.
7
A locus that enhances the induction of endogenous ecotropic murine leukemia viruses is distinct from genome-length ecotropic proviruses.一个增强内源性亲嗜性鼠白血病病毒诱导的基因座与基因组长度的亲嗜性前病毒不同。
J Virol. 1982 Dec;44(3):950-7. doi: 10.1128/JVI.44.3.950-957.1982.
8
Nontumoral, benign ad malignant stages of transformation of a diploid pig cell line. A review.二倍体猪细胞系转化的非肿瘤性、良性及恶性阶段。综述。
Can J Comp Med. 1981 Jul;45(3):279-90.
9
Comparison of the restriction endonuclease maps of unintegrated proviral DNAs from four xenotropic murine leukemia viruses.四种嗜异性小鼠白血病病毒未整合前病毒DNA的限制性内切酶图谱比较
J Virol. 1981 Dec;40(3):963-70. doi: 10.1128/JVI.40.3.963-970.1981.
10
Identification of ecotropic proviral sequences in inbred mouse strains with a cloned subgenomic DNA fragment.用克隆的亚基因组DNA片段鉴定近交系小鼠品系中的嗜亲性前病毒序列。
Proc Natl Acad Sci U S A. 1980 Oct;77(10):5779-83. doi: 10.1073/pnas.77.10.5779.

本文引用的文献

1
Kinetics of renaturation of DNA.DNA复性动力学
J Mol Biol. 1968 Feb 14;31(3):349-70. doi: 10.1016/0022-2836(68)90414-2.
2
A crude nuclease preparation suitable for use in DNA reassociation experiments.一种适用于DNA重缔合实验的粗制核酸酶制剂。
Biochim Biophys Acta. 1971 Jul 29;240(4):522-31. doi: 10.1016/0005-2787(71)90709-x.
3
Induction of murine C-type viruses from clonal lines of virus-free BALB-3T3 cells.从无病毒的BALB-3T3细胞克隆系中诱导出鼠C型病毒。
Science. 1971 Oct 8;174(4005):157-9. doi: 10.1126/science.174.4005.157.
4
Isolation and characterization of bacterial ribosomal RNA cistrons.细菌核糖体RNA顺反子的分离与特性分析。
Biophys J. 1968 Oct;8(10):1104-18. doi: 10.1016/S0006-3495(68)86542-7.
5
Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms.DNA中的重复序列。数以十万计的DNA序列拷贝已被纳入高等生物的基因组中。
Science. 1968 Aug 9;161(3841):529-40. doi: 10.1126/science.161.3841.529.
6
Partial transcription of murine type C viral genomes in BALB c cell lines.BALB c细胞系中小鼠C型病毒基因组的部分转录
J Virol. 1973 Oct;12(4):711-20. doi: 10.1128/JVI.12.4.711-720.1973.
7
Independent segregation of loci for activation of biologically distinguishable RNA C-type viruses in mouse cells.小鼠细胞中生物可区分的RNA C型病毒激活位点的独立分离。
Proc Natl Acad Sci U S A. 1973 Jul;70(7):2055-8. doi: 10.1073/pnas.70.7.2055.
8
Characterization of murine leukaemia virus-specific DNA present in normal mouse cells.正常小鼠细胞中存在的鼠白血病病毒特异性DNA的特性分析。
Nat New Biol. 1973 Jul 18;244(133):76-9. doi: 10.1038/newbio244076a0.
9
Measurement of endogenous leukosis virus nucleotide sequences in the DNA of normal avian embryos by RNA-DNA hybridization.通过RNA-DNA杂交技术检测正常禽胚DNA中内源性白血病病毒核苷酸序列
Virology. 1973 May;53(1):196-203. doi: 10.1016/0042-6822(73)90478-9.
10
Studies of genetic transmission of murine leukemia virus by AKR mice. II. Crosses with Fv-1 b strains of mice.AKR小鼠对鼠白血病病毒的遗传传递研究。II. 与Fv-1 b系小鼠的杂交
J Exp Med. 1972 Nov 1;136(5):1286-301. doi: 10.1084/jem.136.5.1286.

有证据表明,AKR鼠白血病病毒基因组在高病毒血症AKR小鼠的DNA中是完整的,而在“病毒阴性”NIH小鼠的DNA中是不完整的。

Evidence that the AKR murine-leukemia-virus genome is complete in DNA of the high-virus AKR mouse and incomplete in the DNA of the "virus-negative" NIH mouse.

作者信息

Chattopadhyay S K, Lowy D R, Teich N M, Levine A S, Rowe W P

出版信息

Proc Natl Acad Sci U S A. 1974 Jan;71(1):167-71. doi: 10.1073/pnas.71.1.167.

DOI:10.1073/pnas.71.1.167
PMID:4359326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC387958/
Abstract

The AKR mouse has a high titer of murine leukemia virus early in life, and virus-negative cells derived from embryos of this mouse strain can be activated to yield murine leukemia virus by treatment with 5-iododeoxyuridine. In contrast to this high-virus strain, the NIH Swiss mouse has a low incidence of leukemia and no murine leukemia virus has been isolated from it (virus-negative). We have investigated this difference between AKR and NIH mice by examining the sequences specific for murine leukemia virus in nucleic acids of these mice. A single-stranded viral-DNA probe synthesized in vitro using murine-leukemia-virus from the AKR mouse contains at least 87% of the sequences present in the 70S viral RNA; most of these sequences are in proportions similar to their content in the 70S RNA. Using this probe in nucleic acid hybridization experiments, we have shown that NIH-mouse-cell DNA and AKR-mouse-cell DNA differ with respect to sequences specific for AKR murine-leukemia-virus: NIH-mouse-cell DNA lacks some of the virus-specific sequences present in AKR-mouse-cell DNA, and there are two distinct sets of virus-specific sequences in AKR-mouse-cell DNA, whereas there is only one set in NIH-mouse-cell DNA.RNA from virus-negative AKR-mouse cells grown in tissue culture contains some, but not all, virus-specific RNA sequences; however, within 48 hr after initiating treatment of these cells with 5-iododeoxyuridine, the complete viral genome is represented in cellular RNA.

摘要

AKR小鼠在生命早期具有高滴度的鼠白血病病毒,并且源自该小鼠品系胚胎的病毒阴性细胞可以通过用5-碘脱氧尿苷处理而被激活以产生鼠白血病病毒。与这种高病毒品系相反,NIH瑞士小鼠白血病发病率低,且未从其分离出鼠白血病病毒(病毒阴性)。我们通过检查这些小鼠核酸中鼠白血病病毒特有的序列,研究了AKR小鼠和NIH小鼠之间的这种差异。使用来自AKR小鼠的鼠白血病病毒体外合成的单链病毒DNA探针包含70S病毒RNA中至少87%的序列;这些序列中的大多数比例与其在70S RNA中的含量相似。在核酸杂交实验中使用该探针,我们发现NIH小鼠细胞DNA和AKR小鼠细胞DNA在AKR鼠白血病病毒特有的序列方面存在差异:NIH小鼠细胞DNA缺乏AKR小鼠细胞DNA中存在的一些病毒特异性序列,并且AKR小鼠细胞DNA中有两组不同的病毒特异性序列,而NIH小鼠细胞DNA中只有一组。在组织培养中生长的病毒阴性AKR小鼠细胞的RNA包含一些但不是全部病毒特异性RNA序列;然而,在用5-碘脱氧尿苷开始处理这些细胞后的48小时内,完整的病毒基因组出现在细胞RNA中。