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Nuclear factors interacting with an interleukin-6 responsive element of rat α2-macroglobulin gene
Author(s) -
Takashi Ito,
Hiroshi Tanahashi,
Yoshio Musumi,
Yoshiyuki Sakaki
Publication year - 1989
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/17.22.9425
Subject(s) - biology , gene , macroglobulin , conserved sequence , deoxyribonuclease i , regulatory sequence , acute phase protein , gene expression , microbiology and biotechnology , nuclear protein , regulation of gene expression , sequence (biology) , peptide sequence , genetics , inflammation , transcription factor , immunology , base sequence
During acute inflammation, a group of liver-derived plasma proteins, acute phase proteins (APPs), increase in concentration. Interleukin-6 (IL-6) is responsible for this increase via the induction of APP gene expression. We have identified an IL-6 responsive cis-acting element (IL-6RE) of gene encoding a typical APP, rat alpha 2-macroglobulin (alpha 2M). The IL-6RE contains a sequence that is conserved among the 5'-flanking regions of various APP genes. Introduction of mutations into the conserved sequence revealed that the sequence, termed IL-6RE core, is a critical and essential component of IL6-RE. Nuclear factors binding to the IL-6RE core were identified in livers of normal and inflamed rats. Mobility shift pattern and DNase I footprinting profile indicated that the factors from normal and inflamed stages recognized the same sequence but were distinct from each other. These results suggested that the regulation of alpha 2M gene expression may involve mutually exclusive interaction of stage-specific trans-acting factors.

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