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第二个NM23基因NME2定位于染色体17q21 - q22。

Localization of a second NM23 gene, NME2, to chromosome 17q21-q22.

作者信息

Kelsell D P, Black D M, Solomon E, Spurr N K

机构信息

Human Genetic Resources Laboratory, Imperial Cancer Research Fund, Clare Hall Laboratorie, Potters Bar, Hertfordshire, United Kingdom.

出版信息

Genomics. 1993 Aug;17(2):522-4. doi: 10.1006/geno.1993.1362.

Abstract

NM23 is a candidate tumor suppressor protein and has recently been identified as an NDP kinase. The expression of NM23 is inversely related to the metastatic potential of tumor cells. Two NM23 genes, NME1 and NME2, that code for the A and B chains of the kinase, respectively, have been cloned. To determine the human chromosomal location of the NME2 gene, we have analyzed DNA from rodent-human cell lines and hybrid cell lines containing portions of chromosome 17 by a combination of PCR amplification and Southern hybridization. The NME2 gene was mapped to the chromosome region 17q21-q22, the same region in which the NME1 gene has been localized. This region is linked to the early onset breast/ovarian locus (BRCA1) and allelic deletions of NME1 have been associated with metastatic potential of colorectal carcinomas.

摘要

NM23是一种候选肿瘤抑制蛋白,最近被鉴定为核苷二磷酸激酶。NM23的表达与肿瘤细胞的转移潜能呈负相关。分别编码该激酶A链和B链的两个NM23基因,即NME1和NME2,已被克隆。为了确定NME2基因在人类染色体上的位置,我们通过聚合酶链反应(PCR)扩增和Southern杂交相结合的方法,分析了来自啮齿动物-人类细胞系以及含有17号染色体部分片段的杂交细胞系的DNA。NME2基因被定位到17q21-q22染色体区域,该区域与NME1基因所在区域相同。该区域与早发性乳腺癌/卵巢癌基因座(BRCA1)相关,并且NME1的等位基因缺失与结直肠癌的转移潜能有关。

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