EXPRESSION OF A 74-KDA NUCLEAR FACTOR-1 (NF1) PROTEIN IS INDUCED IN MOUSE MAMMARY-GLAND INVOLUTION - INVOLUTION-ENHANCED OCCUPATION OF A TWIN NF1 BINDING-ELEMENT IN THE TESTOSTERONE-REPRESSED PROSTATE MESSAGE-2 CLUSTERTIN PROMOTER/

Citation
Eem. Furlong et al., EXPRESSION OF A 74-KDA NUCLEAR FACTOR-1 (NF1) PROTEIN IS INDUCED IN MOUSE MAMMARY-GLAND INVOLUTION - INVOLUTION-ENHANCED OCCUPATION OF A TWIN NF1 BINDING-ELEMENT IN THE TESTOSTERONE-REPRESSED PROSTATE MESSAGE-2 CLUSTERTIN PROMOTER/, The Journal of biological chemistry, 271(47), 1996, pp. 29688-29697
Citations number
70
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
271
Issue
47
Year of publication
1996
Pages
29688 - 29697
Database
ISI
SICI code
0021-9258(1996)271:47<29688:EOA7NF>2.0.ZU;2-Y
Abstract
Testosterone repressed prostate message-2 (TRPM-2)/clusterin gene expr ession is rapidly induced in early involution of the mouse mammary gla nd, after weaning, and in the rat ventral prostate, after castration, A search for involution-enhanced DNaseI footprints in the proximal mou se TRPM-2/clusterin gene promoter led to the identification and charac terization (by DNase I footprinting and EMSA) of a twin nuclear factor 1 (NF1) binding element at -356/-309, relative to the proposed transc ription start site; nuclear extracts from 2-day involuting mouse mamma ry gland showed an enhanced footprint over the proximal NF1 element; e xtracts from involuting prostate showed enhanced occupancy of both NF1 binding elements. Subsequent EMSA and Western analysis led to the det ection of a 74-kDa NF1 protein whose expression is triggered in early involution in the mouse mammary gland; such an induced protein is not found in the involuting rat ventral prostate, This protein was not fou nd in lactation where three other NF1 proteins of 114, 68, and 46 kDa were detected. Reiteration of the epithelial cell apoptosis associated with early mammary gland involution, in vitro, in a primary cell cult ure system, triggered the appearance of the 74-kDa NF1, Overlaying the cells with laminin-rich extracellular matrix suppressed the apoptosis and the expression of the 74-kDa NF1 and, in the presence of lactogen ic hormones, initiated milk protein gene expression and the expression of two of the lactation-associated NF1 proteins (68 and 46 kDa), This study, thus, identifies for the first time the occurrence of a switch in expression of different members of the family of NF1 transcription factors as mammary epithelial cells move from the differentiated to t he involution/apoptotic state, and it is likely that the involution-sp ecific 74-kDa NF1 accounts for the enhanced NF1 footprint detected on the TRPM-2/clusterin promoter with extracts of mouse mammary gland.