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Fim-1、Fim-2/c-fms和Fim-3是弗氏小鼠白血病病毒在成髓细胞白血病中的三个常见整合位点,分别定位于小鼠的13号、18号和3号染色体上。

Fim-1, Fim-2/c-fms, and Fim-3, three common integration sites of Friend murine leukemia virus in myeloblastic leukemias, map to mouse chromosomes 13, 18, and 3, respectively.

作者信息

Sola B, Simon D, Mattéi M G, Fichelson S, Bordereaux D, Tambourin P E, Guenet J L, Gisselbrecht S

机构信息

Institut National de la Santé et de la Recherche Médicale U152-Centre National de la Recherche Scientifique, UA628, Hôpital Cochin, Paris, France.

出版信息

J Virol. 1988 Nov;62(11):3973-8. doi: 10.1128/JVI.62.11.3973-3978.1988.

Abstract

Three common proviral integration sites, Fim-1, Fim-2/c-fms, and Fim-3, have been described in mouse myeloid leukemias induced by the Friend murine leukemia virus. The nature and function of Fim-1 and Fim-3 are still unknown since no transcript from these loci has been detected so far. To identify these two loci, we undertook their chromosomal localization using restriction fragment length polymorphism detected between C57BL/6 mice and the wild-derived inbred strain of Mus spretus. Using interspecific backcross analysis, we mapped Fim-1 to mouse chromosome 13 and Fim-3 to mouse chromosome 3. Interestingly, Fim-3 is tightly linked to Evi-1, another common integration site of ecotropic virus involved in another model of mouse myeloid leukemogenesis. Fim-2 spans the 5' end of the c-fms gene, which encodes for the macrophage-colony-stimulating factor receptor. We located the c-fms gene on the D band of chromosome 18 by in situ hybridization.

摘要

在由弗瑞德氏鼠白血病病毒诱导的小鼠髓性白血病中,已发现三个常见的前病毒整合位点,即Fim-1、Fim-2/c-fms和Fim-3。由于目前尚未检测到这些基因座的转录本,Fim-1和Fim-3的性质和功能仍不清楚。为了鉴定这两个基因座,我们利用在C57BL/6小鼠和野生来源的近交系小家鼠之间检测到的限制性片段长度多态性对它们进行染色体定位。通过种间回交分析,我们将Fim-1定位到小鼠13号染色体,将Fim-3定位到小鼠3号染色体。有趣的是,Fim-3与Evi-1紧密连锁,Evi-1是嗜亲性病毒的另一个常见整合位点,参与另一种小鼠髓性白血病发生模型。Fim-2跨越c-fms基因的5'端,该基因编码巨噬细胞集落刺激因子受体。我们通过原位杂交将c-fms基因定位到18号染色体的D带。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/864b/253824/b80db11da117/jvirol00090-0072-a.jpg

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