Ellisen L W, Bird J, West D C, Soreng A L, Reynolds T C, Smith S D, Sklar J
Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Cell. 1991 Aug 23;66(4):649-61. doi: 10.1016/0092-8674(91)90111-b.
Previously we described joining of DNA in the beta T cell receptor gene to DNA of an uncharacterized locus in a t(7;9)(q34;q34.3) chromosomal translocation from a case of human T lymphoblastic leukemia (T-ALL). We now show that the locus on chromosome 9 contains a gene highly homologous to the Drosophila gene Notch. Transcripts of the human gene, for which we propose the name TAN-1, and its murine counterpart are present in many normal human fetal and adult mouse tissues, but are most abundant in lymphoid tissues. In t(7;9)(q34;q34.3) translocations from three cases of T-ALL, the breakpoints occur within 100 bp of an intron in TAN-1, resulting in truncation of TAN-1 transcripts. These observations suggest that TAN-1 may be important for normal lymphocyte function and that alteration of TAN-1 may play a role in the pathogenesis of some T cell neoplasms.
先前我们描述了在一例人类T淋巴细胞白血病(T-ALL)患者的t(7;9)(q34;q34.3)染色体易位中,βT细胞受体基因中的DNA与一个未鉴定位点的DNA发生连接。我们现在发现,9号染色体上的这个位点包含一个与果蝇Notch基因高度同源的基因。我们将该人类基因命名为TAN-1,其转录本及其小鼠对应物存在于许多正常人类胎儿和成年小鼠组织中,但在淋巴组织中最为丰富。在三例T-ALL患者的t(7;9)(q34;q34.3)易位中,断点出现在TAN-1基因一个内含子的100 bp范围内,导致TAN-1转录本截短。这些观察结果表明,TAN-1可能对正常淋巴细胞功能很重要,并且TAN-1的改变可能在某些T细胞肿瘤的发病机制中起作用。