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一种潜在原癌基因int-2的人类同源物的特性鉴定与染色体定位

Characterization and chromosome assignment of the human homolog of int-2, a potential proto-oncogene.

作者信息

Casey G, Smith R, McGillivray D, Peters G, Dickson C

出版信息

Mol Cell Biol. 1986 Feb;6(2):502-10. doi: 10.1128/mcb.6.2.502-510.1986.

Abstract

int-2 is one of two cellular genes (int-1 and int-2) currently implicated in the genesis of mammary carcinomas by mouse mammary tumor virus and may constitute a novel cellular proto-oncogene. Using low-stringency hybridization with mouse int-2 probes, we established that homologous genes exist in a variety of mammalian species, including humans, but failed to detect related sequences in other classes and phyla. Recombinant bacteriophage clones and a single cosmid encompassing the human int-2 gene were isolated and characterized by restriction enzyme mapping. A survey of nine primary human breast tumors, three breast tumor cell lines, and three normal individuals revealed no evidence for gross amplification or rearrangement of the int-2 locus. Three distinct restriction fragment length polymorphisms were observed which could prove useful in future linkage studies. By a combination of in situ hybridization of metaphase chromosomes and somatic cell genetics, the human int-2 gene was mapped to chromosome 11, band q13.

摘要

Int-2是目前被认为与小鼠乳腺肿瘤病毒诱发乳腺癌相关的两个细胞基因(int-1和int-2)之一,可能构成一种新的细胞原癌基因。利用与小鼠Int-2探针进行的低严谨度杂交,我们确定在包括人类在内的多种哺乳动物物种中存在同源基因,但在其他类别和门中未检测到相关序列。分离出了包含人类Int-2基因的重组噬菌体克隆和一个黏粒,并通过限制性酶切图谱进行了表征。对9例原发性人类乳腺肿瘤、3个乳腺肿瘤细胞系和3个正常个体的调查显示,没有证据表明Int-2基因座存在明显扩增或重排。观察到三种不同的限制性片段长度多态性,这可能在未来的连锁研究中有用。通过中期染色体原位杂交和体细胞遗传学相结合的方法,将人类Int-2基因定位于11号染色体q13带。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d99/367539/de49003fa90c/molcellb00086-0167-a.jpg

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