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Site-specific rearrangements in the long terminal repeat of extra mouse mammary tumor proviruses in murine T-cell leukemias.

作者信息

Michalides R, Wagenaar E

出版信息

Virology. 1986 Oct 15;154(1):76-84. doi: 10.1016/0042-6822(86)90431-9.

DOI:10.1016/0042-6822(86)90431-9
PMID:3019010
Abstract

Extra MMTV proviruses in T-cell leukemias of GR and C57/BL10 mice contain alterations in their long terminal repeat (LTR) sequence. The four different leukemias studied contain different deletions, but common hallmarks were observed around the recombination sites. At the 5' end of the deletions we observed a common nonamer sequence, AGACAGGTG, in two leukemias and an almost identical sequence, AGAGCAGGTG, in two other leukemias. At the 3' end of the deletions we invariably found a common stretch of five nucleotides, TTAAA. Three of the four leukemias showed nonconserved crossover sites. The deletions in two leukemias were replaced with neighboring sequences, generating direct repeats. The MMTV LTR characteristic open reading frame and glucocorticoid response element were altered in all four rearranged MMTV LTRs. These results demonstrate site specific rearrangements in the LTR of extra MMTV proviruses in T-cell leukemias and suggest that these rearrangements might permit expression of MMTV in a new target cell.

摘要

相似文献

1
Site-specific rearrangements in the long terminal repeat of extra mouse mammary tumor proviruses in murine T-cell leukemias.
Virology. 1986 Oct 15;154(1):76-84. doi: 10.1016/0042-6822(86)90431-9.
2
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3
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Extra mouse mammary tumor proviruses in DBA/2 mouse lymphomas acquire a selective advantage in lymphocytes by alteration in the U3 region of the long terminal repeat.DBA/2小鼠淋巴瘤中额外的小鼠乳腺肿瘤前病毒通过长末端重复序列U3区域的改变在淋巴细胞中获得选择性优势。
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Expression of the protein product of the mouse mammary tumor virus long terminal repeat gene in phorbol ester-treated mouse T-cell-leukemia cells.小鼠乳腺肿瘤病毒长末端重复基因的蛋白质产物在佛波酯处理的小鼠T细胞白血病细胞中的表达。
J Virol. 1986 May;58(2):441-9. doi: 10.1128/JVI.58.2.441-449.1986.

引用本文的文献

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J Virol. 2000 Oct;74(20):9786-91. doi: 10.1128/jvi.74.20.9786-9791.2000.
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