THE PROLACTIN-INDUCIBLE PROTEIN (PIP GCDFP-15) GENE - CLONING, STRUCTURE AND REGULATION

被引:69
作者
MYAL, Y
ROBINSON, DB
IWASIOW, B
TSUYUKI, D
WONG, P
SHIU, RPC
机构
[1] UNIV MANITOBA, FAC MED, DEPT PHYSIOL, WINNIPEG R3E 0W3, MANITOBA, CANADA
[2] UNIV OTTAWA, DEPT BIOCHEM, OTTAWA K1H 8M5, ONTARIO, CANADA
关键词
PROLACTIN-INDUCIBLE PROTEIN; GROSS CYSTIC DISEASE FLUID PROTEIN; CLONING; SEQUENCE; MESSENGER RNA STABILITY; NUCLEAR TRANSCRIPTION; HUMAN-BREAST CANCER; BETA-CASEIN GENE; RIBONUCLEIC-ACID; CELL-LINE; C-MYC; EXPRESSION; ESTROGEN; TRANSCRIPTION; OVALBUMIN; SEQUENCES;
D O I
10.1016/0303-7207(91)90153-J
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The androgen and prolactin responsive prolactin-inducible protein (PIP)/gross cystic disease fluid protein (GCDFP-15) is expressed in benign and malignant human breast tumors and in such normal exocrine organs as sweat, salivary and lacrimal glands. In this paper we report the cloning and structure of the human gene, and describe potential mechanisms involved in its regulation by hormones. The entire PIP gene, 7 kb long, was found in a single recombinant phage clone. The gene has 4 exons ranging from 106 bp to 223 bp in length. Nuclear run-on experiments utilizing PIP genomic fragments to detect nascent PIP transcripts revealed that both androgen and prolactin increased transcription of the PIP gene. Neither hormone had any effect on the stability of PIP precursor RNA or mature mRNA. Therefore the PIP gene is an excellent model by which to study the molecular events associated with the actions of prolactin and androgen in the regulation of gene expression in mammalian cells.
引用
收藏
页码:165 / 175
页数:11
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