Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.1.27.1 (
RNase
)
16,360
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Metal activation of metallothionein gene transcription depends mainly on the presence of regulatory DNA sequences termed metal-regulatory elements (MREs) and involves
MRE-binding transcription factor-1
(
MTF-1
) interacting with the MREs in a Zn(2+)-dependent manner. We previously identified and characterized a nuclear protein, termed metal element protein-1 (MEP-1), specifically binding with high affinity to MRE elements. The precise relationship between
MTF-1
and MEP-1 was unclear, and to determine whether MEP-1 and
MTF-1
were distinct protein species, we performed DNA binding analyses to characterize the binding properties of both proteins. Electrophoretic mobility-shift assays showed that
MTF-1
, produced in COS cells, produces a slower-migrating band compared with that obtained with purified MEP-1. Using an anti-
MTF-1
antibody, we showed that both the
MTF-1
-MRE and the MEP-1-MRE complexes are supershifted by an anti-
MTF-1
antibody, thus demonstrating that MEP-1 is antigenically related to
MTF-1
.
RNase
protection analyses carried out with RNA prepared from different tissues and cell lines failed to reveal the presence of
MTF-1
splicing variants. This indicates that MEP-1 may be a proteolytic fragment of
MTF-1
.
MTF-1
DNA-binding activity was rapidly activated in vivo by Zn(2+) ions but not by Cd(2+), UV irradiation or PMA, and occurred on ice as well as at 21 degrees C. In control and Zn(2+)-treated cell extracts, DNA-binding activity was not enhanced in vitro following the addition of exogenous Zn(2+) or a preincubation at 37 degrees C. However, recombinant
MTF-1
produced in vitro required Zn(2+) activation for DNA binding. Interestingly, treatment of nuclear extracts with calf intestine phosphatase completely abrogated
MTF-1
DNA-binding activity, thus suggesting that phosphorylation is involved in the regulation of
MTF-1
activity.
...
PMID:Characterization of the mouse metal-regulatory-element-binding proteins, metal element protein-1 and metal regulatory transcription factor-1. 1117 Oct 56