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淋巴细胞特异性蛋白酪氨酸激酶基因(lck)在人类淋巴瘤常见染色体异常位点的定位。

Localization of a lymphocyte-specific protein tyrosine kinase gene (lck) at a site of frequent chromosomal abnormalities in human lymphomas.

作者信息

Marth J D, Disteche C, Pravtcheva D, Ruddle F, Krebs E G, Perlmutter R M

出版信息

Proc Natl Acad Sci U S A. 1986 Oct;83(19):7400-4. doi: 10.1073/pnas.83.19.7400.

Abstract

The murine lck gene is closely related to a family of cellular protooncogenes and encodes a lymphocyte-specific, membrane-associated protein tyrosine kinase. We and others have demonstrated that the lck gene is rearranged and overexpressed in the murine lymphoma LSTRA, most likely as a result of the insertion of Moloney murine leukemia virus DNA immediately adjacent to the gene. We now report that the lck gene is located at the distal end of murine chromosome 4 and on human chromosome 1 at position 1p32-35 near a site of frequent structural abnormalities in human lymphomas and neuroblastomas. These results raise the possibility that structural alteration of the lck gene through chromosomal rearrangement may contribute to transformation in human malignant disease.

摘要

小鼠lck基因与一组细胞原癌基因密切相关,编码一种淋巴细胞特异性的、与膜相关的蛋白酪氨酸激酶。我们和其他人已经证明,lck基因在小鼠淋巴瘤LSTRA中发生重排并过表达,很可能是莫洛尼鼠白血病病毒DNA插入到该基因紧邻位置的结果。我们现在报告,lck基因位于小鼠4号染色体的远端,在人类染色体1上位于1p32 - 35位置,靠近人类淋巴瘤和神经母细胞瘤中频繁出现结构异常的位点。这些结果增加了一种可能性,即通过染色体重排导致的lck基因结构改变可能在人类恶性疾病的转化中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2fb/386725/3b50d9b9260c/pnas00323-0282-a.jpg

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