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Retrovirus-induced insertional mutagenesis: mechanism of collagen mutation in Mov13 mice.

作者信息

Barker D D, Wu H, Hartung S, Breindl M, Jaenisch R

机构信息

Whitehead Institute for Biomedical Research, Nine Cambridge Center, Massachusetts.

出版信息

Mol Cell Biol. 1991 Oct;11(10):5154-63. doi: 10.1128/mcb.11.10.5154-5163.1991.

DOI:10.1128/mcb.11.10.5154-5163.1991
PMID:1922037
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC361539/
Abstract

The Mov13 mouse strain carries a mutation in the alpha 1(I) procollagen gene which is due to the insertion of a Moloney murine leukemia provirus into the first intron. This insertion results in the de novo methylation of the provirus and flanking DNA, the alteration of chromatin structure, and the transcriptional inactivity of the collagen promoter. To address the mechanism of mutagenesis, we reintroduced a cloned and therefore demethylated version of the Mov13 mutant allele into mouse fibroblasts. The transfected gene was not transcribed, indicating that the transcriptional defect was not due to the hypermethylation. Rather, this result strongly suggests that the mutation is due to the displacement or disruption of cis-acting regulatory DNA sequences within the first intron. We also constructed a Mov13 variant allele containing a single long terminal repeat instead of the whole provirus. This construct also failed to express mRNA, indicating that the Mov13 mutation does not revert by provirus excision as has been observed for other retrovirus-induced mutations.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/f027327c83e6/molcellb00034-0366-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/80556d4b0b84/molcellb00034-0363-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/a58212474e5a/molcellb00034-0364-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/659635fa8eb3/molcellb00034-0365-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/1263f4b65616/molcellb00034-0365-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/f027327c83e6/molcellb00034-0366-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/80556d4b0b84/molcellb00034-0363-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/a58212474e5a/molcellb00034-0364-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/659635fa8eb3/molcellb00034-0365-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/1263f4b65616/molcellb00034-0365-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e5/361539/f027327c83e6/molcellb00034-0366-a.jpg

相似文献

1
Retrovirus-induced insertional mutagenesis: mechanism of collagen mutation in Mov13 mice.
Mol Cell Biol. 1991 Oct;11(10):5154-63. doi: 10.1128/mcb.11.10.5154-5163.1991.
2
Retrovirus-induced interference with collagen I gene expression in Mov13 fibroblasts is maintained in the absence of DNA methylation.逆转录病毒诱导的对Mov13成纤维细胞中I型胶原基因表达的干扰在不存在DNA甲基化的情况下仍会持续。
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3
Retrovirus-induced insertional mutation in Mov13 mice affects collagen I expression in a tissue-specific manner.
Cell. 1989 Jun 2;57(5):807-16. doi: 10.1016/0092-8674(89)90795-2.
4
Retrovirus-induced de novo methylation of flanking host sequences correlates with gene inactivity.
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5
Transcription of a mutant collagen I gene is a cell type and stage-specific marker for odontoblast and osteoblast differentiation.
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Tissue- and stage-specific activation of an endogenous provirus after transcription through its integration site in the opposite orientation.通过其整合位点以相反方向转录后内源性前病毒的组织和阶段特异性激活。
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Retrovirus insertion inactivates mouse alpha 1(I) collagen gene by blocking initiation of transcription.逆转录病毒插入通过阻断转录起始使小鼠α1(I)胶原蛋白基因失活。
Nature. 1986;320(6060):365-7. doi: 10.1038/320365a0.
8
Restricted expression of Mov13 mutant alpha 1(I) collagen gene in osteoblasts and its consequences for bone development.
Dev Dyn. 1993 Dec;198(4):273-83. doi: 10.1002/aja.1001980405.
9
Isolation of an integrated provirus of Moloney murine leukemia virus with long terminal repeats in inverted orientation: integration utilizing two U3 sequences.分离出具有反向长末端重复序列的莫洛尼鼠白血病病毒整合前病毒:利用两个U3序列进行整合。
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10
Retrovirus-induced lethal mutation in collagen I gene of mice is associated with an altered chromatin structure.逆转录病毒诱导的小鼠I型胶原蛋白基因致死性突变与染色质结构改变有关。
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引用本文的文献

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2
Mutation of SENP1/SuPr-2 reveals an essential role for desumoylation in mouse development.SENP1/SuPr-2的突变揭示了去SUMO化在小鼠发育中的重要作用。
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3
Collagen alpha1(I) gene (COL1A1) is repressed by RFX family.胶原蛋白α1(I)基因(COL1A1)受RFX家族抑制。

本文引用的文献

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Molecular analysis of large transposable elements carrying the white locus of Drosophila melanogaster.大转座子携带的果蝇黑素体的白色基因座的分子分析。
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