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/
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
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.