Gallahan D, Callahan R
Laboratory of Tumor Immunology and Biology, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA.
Oncogene. 1997 Apr 24;14(16):1883-90. doi: 10.1038/sj.onc.1201035.
The INT3 gene is frequently rearranged in mouse mammary tumor virus (MMTV)-induced mammary tumors of the CzechII mouse strain. We have completed the nucleotide sequence of the normal 6.5 Kb INT3 RNA and defined the intron/exon boundaries of the gene. The open reading frame of INT3 RNA should encode a 200 kd protein which shares 60% homology with the mouse homologue of Drosophila NOTCH. INT3 is unique among other members of the NOTCH family by containing 29 instead of 36 EGF-like repeats in the extracellular domain of the gene product. Five novel EGF-like repeats have been created as consequence of apparent small deletions which have occurred within the coding region for the extracellular domain during evolution. Nucleotide sequence analysis of host-viral junction fragments from nine independent MMTV-induced mammary tumors containing a rearranged INT3 gene reveals that all of the integration events occur within a 174 bp region 3' of the sequences encoding the LIN12 repeats in the INT3 extracellular domain and 5' of the sequences encoding the transmembrane domain. Therefore, the only tumorigenic INT3 mutations resulting from MMTV proviral insertions are those which results in the expression of the intracellular domain. This strongly suggests that MMTV-induced activation of INT3 is manifest in the absence of the regulatory action of the extracellular domain, including the LIN12 repeat sequences, leaving the expressed intracellular domain constitutively free to function in its role in mammary tumorigenesis.
INT3基因在捷克II小鼠品系的小鼠乳腺肿瘤病毒(MMTV)诱导的乳腺肿瘤中经常发生重排。我们已经完成了正常6.5 Kb INT3 RNA的核苷酸序列测定,并确定了该基因的内含子/外显子边界。INT3 RNA的开放阅读框应编码一种200 kd的蛋白质,该蛋白质与果蝇NOTCH的小鼠同源物具有60%的同源性。INT3在NOTCH家族的其他成员中是独特的,因为其基因产物的细胞外结构域含有29个而非36个EGF样重复序列。由于在进化过程中细胞外结构域编码区域内发生了明显的小缺失,产生了五个新的EGF样重复序列。对来自九个独立的含有重排INT3基因的MMTV诱导的乳腺肿瘤的宿主-病毒连接片段进行核苷酸序列分析,结果显示所有整合事件均发生在INT3细胞外结构域中编码LIN12重复序列的序列3'端的174 bp区域内以及编码跨膜结构域的序列5'端。因此,MMTV前病毒插入导致的唯一致瘤性INT3突变是那些导致细胞内结构域表达的突变。这强烈表明,MMTV诱导的INT3激活在没有细胞外结构域(包括LIN12重复序列)的调节作用的情况下表现出来,使得表达的细胞内结构域能够持续自由地发挥其在乳腺肿瘤发生中的作用。