PROLACTIN (PRL)-DEPENDENT EXPRESSION OF A ZINC-FINGER PROTEIN-ENCODING GENE, GFI-1, IN NB2 LYMPHOMA-CELLS - CONSTITUTIVE EXPRESSION IN AUTONOMOUS SUBLINES

被引:11
作者
GILKS, CB
PORTER, SD
BARKER, C
TSICHLIS, PN
GOUT, PW
机构
[1] BRITISH COLUMBIA CANC AGCY, DEPT CANC ENDOCRINOL, VANCOUVER, BC V5Z 4E6, CANADA
[2] UNIV BRITISH COLUMBIA, DEPT PATHOL, VANCOUVER, BC, CANADA
[3] FOX CHASE CANC CTR, PHILADELPHIA, PA 19111 USA
关键词
D O I
10.1210/en.136.4.1805
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The proliferation of cultured rat Nb2 lymphoma cells is dependent on prolactin (PRL) acting as the principal growth factor. Previously, PRL-independent Nb2 sublines were obtained by PRL starvation of the parent line and cloning of surviving cells. Development of PRL independence was in some cases found to be associated with a reciprocal translocation involving chromosome 14 at breakpoint 14p22. In the present study, a novel, 14p22 zinc finger protein-encoding gene, Gfi-1, has been examined for a role in Nb2 cell proliferation. PRL-dependent Nb2 cells expressed the gene during active growth; in comparison, in stationary, early G1-arrested cells obtained by an 18 hr lactogen starvation, Gfi-1 gene expression was markedly decreased. Addition of PRL to such stationary cells led to induction of Gfi-1 gene expression within a few hr with a maximum in late G1. Actively growing cells from 5 different PRL-independent Nb2 sublines, cultured in chemically defined, mitogen-free medium, expressed the gene constitutively. In two sublines, carrying the 14p22 rearrangement, the gene was markedly overexpressed. The results suggest the Gfi-1 gene product has a regulatory role in Nb2 cell mitogenesis and that unscheduled activation could contribute to loss of PRL dependency.
引用
收藏
页码:1805 / 1808
页数:4
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