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PMID: 2082185 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

5'-Heterogeneity in human progesterone receptor transcripts predicts a new amino-terminal truncated "C"-receptor and unique A-receptor messages.

Molecular endocrinology (Baltimore, Md.) ·Vol. 4 ·No. 12 ·1990-12-00 ·Pages 1833-40

Wei LL, Gonzalez-Aller C, Wood WM, Miller LA, Horwitz KB

Abstract

Human progesterone receptors (PR) are thought to comprise two naturally occurring hormone-binding proteins: 94-kDa A-receptors and 120-kDa B-receptors. In this paper we present evidence for a third human PR, an N-terminally truncated, 45- to 50-kDa species, termed the C-receptor. To determine the translational origin of B- and A-receptors we mapped the multiple messages that code for human PR by Northern blot analyses, using a series of oligonucleotides and cDNA fragment probes corresponding to different regions of the PR message. In addition to the six transcripts of 2.5, 3.2, 4.5, 5.2, 6.1, and 11.4 kilobases (kb) originally described, we found that the 11.4-kb species is a complex of four bands that we have termed I-IV. Analysis of poly(A)+ RNA derived from T47Dv human breast cancer cells using a variety of 5'-specific probes has identified three separate structural classes of human PR transcripts, indicating extensive 5'-termini heterogeneity. Class A messages, the 2.5- and 5.2-kb species, lack the sequences surrounding AUGB (codon 1), which is the translation initiation site for B-receptors, but contain AUGA (codon 165), the initiation site for A-receptors, and, therefore, potentially encode only the latter. Class B messages, consisting of the 3.2-, 4.5-, and 6.1-kb species as well as bands I and II of the 11.4-kb complex contain both AUGB and AUGA and could encode both receptor forms.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Base Sequence Binding Sites Breast Neoplasms Chromosome Mapping Codon DNA Probes Humans Methionine/genetics Molecular Sequence Data Molecular Weight Nucleic Acid Hybridization Oligonucleotide Probes Protein Biosynthesis RNA, Messenger/genetics Receptors, Progesterone/chemistry,genetics Transcription, Genetic Tumor Cells, Cultured
Chemicals
Codon DNA Probes Oligonucleotide Probes RNA, Messenger Receptors, Progesterone Methionine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wei L L
Department of Medicine, University of Colorado Health Sciences Center, Denver 80262.
Gonzalez-Aller C
Wood W M
Miller L A
Horwitz K B
Article Info
Journal
Molecular endocrinology (Baltimore, Md.)
Abbr.
Mol Endocrinol
ISSN
0888-8809
Published
1990-12-00
Pages
1833-40
Language
English
Region
United States
NLM ID
8801431
Subset
IM
Grants
NCI NIH HHS · CA-26869 · United States
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